Disease on EC 7.2.2.3 - P-type Na+ transporter
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Acidosis
Enzymatic and functional evidence for adaptation of the vacuolar H(+)-ATPase in proximal tubule apical membranes from rats with chronic metabolic acidosis.
Acidosis
Lactic acidosis progressively impairs dopamine uptake in rat striatal synaptosomes by a mechanism partially independent of the Na+/K+-ATPase dysfunction.
Acidosis
[Effect of acidosis on membrane potential and calcium transport in rat brain synaptosomes]
Acidosis, Lactic
Lactic acidosis progressively impairs dopamine uptake in rat striatal synaptosomes by a mechanism partially independent of the Na+/K+-ATPase dysfunction.
Acidosis, Renal Tubular
An immunocytochemical study of H+ ATPase in kidney transplant rejection.
Acidosis, Renal Tubular
Environmental distal renal tubular acidosis in Thailand: an enigma.
Acquired Immunodeficiency Syndrome
Cytochemical localization of Na+/K+-ATPase activity in cochlear strial marginal cells after various catecholamine administrations.
Acromegaly
Basal metabolic rate in adults with growth hormone deficiency and in patients with acromegaly: relationship with lean body mass, plasma insulin level and leucocyte sodium pump activity.
Acromegaly
Evidence of an endogenous digitalis-like factor in the plasma of patients with acromegaly.
Acromegaly
Increased activity of digoxin-like substance in low-renin hypertension in acromegaly.
Acute Kidney Injury
Effects of acute and chronic uremia on active cation transport in rat myocardium.
Acute Kidney Injury
The pathophysiology of septic shock: acute renal failure in rats following live E coli injection. A histochemical study of the proximal tubules.
Adenocarcinoma
Comparison of adenosine triphosphatase activity of nuclei and mitochondria from mouse mammary adenocarcinoma.
Adenocarcinoma
Identification of Proteins Whose Interaction with Na+,K+-ATPase Is Triggered by Ouabain.
Adenocarcinoma
Immunohistochemical localization of sodium-potassium-stimulated adenosine triphosphatase and carbonic anhydrase in human colon and colonic neoplasms.
Adenocarcinoma
Oxidative Stress and Apoptotic Responses Elicited by Nostoc-Synthesized Silver Nanoparticles against Different Cancer Cell Lines.
Adenocarcinoma of Lung
[Expression of Copper-Transporting P-Type Adenosine Triphosphatase (ATP7B) Correlates with Cisplatin-Resistance in Human Lung Adenocarcinoma Cell Line A549.]
Adenocarcinoma, Papillary
Immunohistochemical and histochemical markers of primary lung cancer, lung metastases, and pleural mesotheliomas.
Adenoma
Gene mutations that promote adrenal aldosterone production, sodium retention, and hypertension.
Adenoma
Immunohistochemical localization of sodium-potassium-stimulated adenosine triphosphatase and carbonic anhydrase in human colon and colonic neoplasms.
Adenoma
[Enzymatic activity of adenosine triphosphatase and acid phosphatase in adenoma of the tongue]
Adenoma, Oxyphilic
Mitochondrial adenosine triphosphatase in the oxyphil cells of a renal oncocytoma.
Adenoma, Pleomorphic
A cytochemical study on the salivary gland pleomorphic adenoma (mixed tumor) and the fetal and adult salivary gland.
Albuminuria
Hyperaldosteronemia and activation of the epithelial sodium channel are not required for sodium retention in puromycin-induced nephrosis.
Alkalosis
Is the alkaline tide a signal to activate metabolic or ionoregulatory enzymes in the dogfish shark (Squalus acanthias)?
Alkalosis
Recovery from blood alkalosis in the Pacific hagfish (Eptatretus stoutii): involvement of gill V-H+-ATPase and Na+/K+-ATPase.
Altitude Sickness
Transport ATPases in the erythrocytes of rats acclimatized to intermittent altitude hypoxia.
Alzheimer Disease
Alzheimer A? Assemblies Accumulate in Excitatory Neurons upon Proteasome Inhibition and Kill Nearby NAK?3 Neurons by Secretion.
Alzheimer Disease
Effect of a purine derivative containing selenium to improve memory decline and anxiety through modulation of the cholinergic system and Na+/K+-ATPase in an Alzheimer's disease model.
Alzheimer Disease
Genetic variability in copper-transporting P-type adenosine triphosphatase (ATP7B) is associated with Alzheimer's disease in a Chinese population.
Alzheimer Disease
Phosphatidylinositol and PI-4-monophosphate recover amyloid beta protein-induced inhibition of Cl- -ATPase activity.
Alzheimer Disease
Regulation of the frontocortical sodium pump by Na+ in Alzheimer's disease: difference from the age-matched control but similarity to the rat model.
Alzheimer Disease
Specificity of biophysical and biochemical alterations in erythrocyte membranes in neurological disorders--Huntington's disease, Friedreich's ataxia, Alzheimer's disease, amyotrophic lateral sclerosis, and myotonic and duchenne muscular dystrophy.
Amyotrophic Lateral Sclerosis
Sodium Pumps Mediate Activity-Dependent Changes in Mammalian Motor Networks.
Amyotrophic Lateral Sclerosis
Specificity of biophysical and biochemical alterations in erythrocyte membranes in neurological disorders--Huntington's disease, Friedreich's ataxia, Alzheimer's disease, amyotrophic lateral sclerosis, and myotonic and duchenne muscular dystrophy.
Anemia
Abnormalities in adenosine triphosphatase of the erythrocyte membrane in iron deficiency anaemia.
Anemia
[Some data on the activity of adenosine triphosphatase and acetylcholinesterase in the erythrocytes of patients with various forms of anemia]
Anemia
[Studies on renal anemias. 3. The behavior of the phosphoric esters of adenosine and adenosine triphosphatase of the erythrocytes in hyperazotemic states]
Anemia, Hemolytic
A new mutation of Wilson's disease P-type ATPase gene in a patient with cirrhosis and coombs-positive hemolytic anemia.
Anemia, Hemolytic
Congenital non-spherocytic haemolytic anaemia variants with primary and secondary pyruvate kinase deficiency. II. Enzymatic studies.
Anemia, Hemolytic
[Adenosine triphosphatase (ATP-ase) deficiency in a family with nonspherocytic hemolytic anemia]
Anemia, Hemolytic
[Adenosine triphosphatase activity in normal persons and patients with hemolytic anemia]
Anemia, Hemolytic
[Experimental hemolytic anemia induced by hetero-antisera. I. Behavior of the adenosine triphosphatase activity of erythrocytes.]
Anemia, Iron-Deficiency
Abnormalities in adenosine triphosphatase of the erythrocyte membrane in iron deficiency anaemia.
Anemia, Pernicious
Fas/CD95 is required for gastric mucosal damage in autoimmune gastritis.
Anemia, Pernicious
Monoclonal antibodies specific for the core protein of the beta-subunit of the gastric proton pump (H+/K+ ATPase). An autoantigen targetted in pernicious anaemia.
Aneurysm
A Novel ATP1A2 Gene Variant Associated With Pure Sporadic Hemiplegic Migraine Improved After Patent Foramen Ovale Closure: A Case Report.
Apnea
2B.03: URIC ACID LEVELS RELATED TO OBSTRUCTIVE SLEEP APNEA SYNDROME IN PATIENTS WITH HYPERTENSION FROM XINJIANG OF CHINA.
Arrhythmias, Cardiac
Angiotensin receptor-neprilysin inhibitior (thiorphan/irbesartan) decreased ischemia-reperfusion induced ventricular arrhythmias in rat; in vivo study.
Arrhythmias, Cardiac
Beneficial effect of eplerenone on cardiac remodelling and electrical properties of the failing heart.
Arrhythmias, Cardiac
Cardenolides: Insights from chemical structure and pharmacological utility.
Arrhythmias, Cardiac
Digitalis toxicity: lack of marked effect on brain na+,k+-adenosine triphosphatase in the cat.
Arrhythmias, Cardiac
Evidence against an involvement of Na+, K+-ATPase in antiarrhythmic mechanism of phenytoin.
Arrhythmias, Cardiac
Exposure to low-level metalaxyl impacts the cardiac development and function of zebrafish embryos.
Arrhythmias, Cardiac
Investigation of cardiac glycosides from oleander in a human induced pluripotent stem cells derived cardiomyocyte model.
Arrhythmias, Cardiac
The cardiac glycoside ouabain activates NLRP3 inflammasomes and promotes cardiac inflammation and dysfunction.
Arteriosclerosis
[Studies on arteriosclerosis and endangitis obliterans. VIII. Hexokinase and adenosine triphosphatase in skeletal muscles in peripheral vascular disorders.]
Arthritis, Rheumatoid
Decreased NA+, K+-ATPase activity in erythrocyte membrane from rheumatoid arthritis patients.
Arthrogryposis
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.
Arthrogryposis
Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations.
Asthma
Decreased sodium-potassium and calcium adenosine triphosphatase activity in asthma: modulation by inhaled and oral corticosteroids.
Asthma
Increased intracellular calcium and decreased activities of leucocyte Na+,K+-ATPase and Ca2+-ATPase in asthma.
Astrocytoma
Sodium-potassium adenosine triphosphatase activity in N-nitrosomethylurea-induced rat astrocytoma cells.
Ataxia
A novel ATP1A2 variant associated with severe stepwise regression, hemiplegia, epilepsy and movement disorders in two unrelated patients.
Ataxia
High mitochondrial DNA T8993G mutation (<90%) without typical features of Leigh's and NARP syndromes.
Ataxia
Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4.
Ataxia
Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures.
Atrial Fibrillation
Cardenolides: Insights from chemical structure and pharmacological utility.
Atrial Fibrillation
Down-regulation of L-type calcium channel and sarcoplasmic reticular Ca(2+)-ATPase mRNA in human atrial fibrillation without significant change in the mRNA of ryanodine receptor, calsequestrin and phospholamban: an insight into the mechanism of atrial electrical remodeling.
Bacteremia
The pathophysiology of septic shock: acute renal failure in rats following live E coli injection. A histochemical study of the proximal tubules.
Bartter Syndrome
The effect of long-term treatment with spironolactone on sodium pump abnormalities in the red blood cells of patients with Bartter's syndrome.
Bone Resorption
Comparative analysis of the effects of a novel vacuolar adenosine 5'-triphosphatase inhibitor, FR202126, and doxycycline on bone loss caused by experimental periodontitis in rats.
Bone Resorption
Metabolic activation stimulates acid secretion and expression of matrix degrading proteases in human osteoblasts.
Bone Resorption
Proton pumping V-ATPase inhibitor bafilomycin A1 affects Rab7 lysosomal localization and abolishes anterograde trafficking of osteoclast secretory lysosomes.
Bradycardia
Mechanism in bradycardia induced by Trimethyltin chloride: Inhibition activity and expression of Na+/K+-ATPase and apoptosis in myocardia.
Bradycardia
Mutation of the Na+/K+-ATPase Atp1a1a.1 causes QT interval prolongation and bradycardia in zebrafish.
Brain Diseases
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.
Brain Diseases
Early onset severe ATP1A2 epileptic encephalopathy: Clinical characteristics and underlying mutations.
Brain Diseases
Early Treatment in Acute Severe Encephalopathy Caused by ATP1A2 Mutation of Familial Hemiplegic Migraine Type 2: Case Report and Literature Review.
Brain Diseases
Familial Hemiplegic Migraine With Asymmetric Encephalopathy Secondary to ATP1A2 Mutation: A Case Series.
Brain Diseases
Na+/K+-ATPase activity and GABA uptake in astroglial cell-enriched fractions and synaptosomes derived from rats in the early stage of experimental hepatogenic encephalopathy.
Brain Edema
Brain damage related to hemorrhagic transformation following cerebral ischemia and the role of K ATP channels.
Brain Edema
Effects of repeated brain ischemia induced by rapid lower body negative pressure on brain water and Na+,K+-ATPase activity in rats.
Brain Edema
Inhibition of rat brain Na+,K+-ATPase activity by serum from patients with fulminant hepatic failure.
Brain Edema
Neurologic manifestations of diabetic comas: correlation with biochemical alterations in the brain.
Brain Edema
Potassium Aspartate Attenuates Brain Injury Induced by Controlled Cortical Impact in Rats Through Increasing Adenosine Triphosphate (ATP) Levels, Na+/K+-ATPase Activity and Reducing Brain Edema.
Brain Edema
The endogenous ouabain-like sodium pump inhibitor in cold injury-induced brain edema.
Brain Injuries
Down-regulated Na(+)/K(+)-ATPase activity in ischemic penumbra after focal cerebral ischemia/reperfusion in rats.
Brain Injuries
Na+,K+-ATPase activity impairment after experimental traumatic brain injury: relationship to spatial learning deficits and oxidative stress.
Brain Injuries
Polymorphisms in migraine-associated gene, atp1a2, and ischemic stroke risk in a biracial population: the genetics of early onset stroke study.
Brain Injuries
Potassium Aspartate Attenuates Brain Injury Induced by Controlled Cortical Impact in Rats Through Increasing Adenosine Triphosphate (ATP) Levels, Na+/K+-ATPase Activity and Reducing Brain Edema.
Brain Injuries
[Study on regulation of tanshinone II(A) on GFAP and ATPase and PDI of cerebral ischemia reperfusion injury in rats].
Brain Injuries, Traumatic
Na+,K+-ATPase activity impairment after experimental traumatic brain injury: relationship to spatial learning deficits and oxidative stress.
Brain Ischemia
Combined actions of Na/K-ATPase, NCX1 and glutamate dependent NMDA receptors in ischemic rat brain penumbra.
Brain Ischemia
Effect of deferoxamine on Na+K+ATPase activity after cerebral ischemia in rabbits.
Brain Ischemia
Effects of repeated brain ischemia induced by rapid lower body negative pressure on brain water and Na+,K+-ATPase activity in rats.
Brain Ischemia
Preconditioning prevents the inhibition of Na+,K+-ATPase activity after brain ischemia.
Brain Ischemia
The influence of MK-801 on the hippocampal free arachidonic acid level and Na+,K+-ATPase activity in global cerebral ischemia-exposed rats.
Brain Ischemia
[Study on regulation of tanshinone II(A) on GFAP and ATPase and PDI of cerebral ischemia reperfusion injury in rats].
Brain Neoplasms
Present and potential future adjuvant issues in high-grade astrocytic glioma treatment.
Brain Neoplasms
Spider venom components decrease glioblastoma cell migration and invasion through RhoA-ROCK and Na+/K+-ATPase ?2: potential molecular entities to treat invasive brain cancer.
Breast Neoplasms
An easy and fast adenosine 5'-diphosphate quantification procedure based on hydrophilic interaction liquid chromatography-high resolution tandem mass spectrometry for determination of the in vitro adenosine 5'-triphosphatase activity of the human breast cancer resistance protein ABCG2.
Breast Neoplasms
BRIP1 inhibits the tumorigenic properties of cervical cancer by regulating RhoA GTPase activity.
Breast Neoplasms
Copper-transporting P-type adenosine triphosphatase (ATP7B) is expressed in human breast carcinoma.
Breast Neoplasms
Digitalis-induced signaling by Na+/K+-ATPase in human breast cancer cells.
Breast Neoplasms
Glyceraldehyde-3-phosphate dehydrogenase as a surface associated antigen on human breast cancer cell lines MACL-1 and MGSO-3.
Breast Neoplasms
Identification of a sodium pump Na+/K+ ATPase ?1-targeted peptide for PET imaging of breast cancer.
Breast Neoplasms
Inner Blood-Retinal Barrier Dominantly Expresses Breast Cancer Resistance Protein: Comparative Quantitative Targeted Absolute Proteomics Study of CNS Barriers in Pig.
Breast Neoplasms
Oleandrin, a cardiac glycoside, induces immunogenic cell death via the PERK/elF2?/ATF4/CHOP pathway in breast cancer.
Breast Neoplasms
On the importance and mechanism of amplification of digitalis signal through Na+/K+-ATPase.
Breast Neoplasms
Oxidative Stress and Apoptotic Responses Elicited by Nostoc-Synthesized Silver Nanoparticles against Different Cancer Cell Lines.
Breast Neoplasms
Pentoxifylline and its major oxidative metabolites exhibit different pharmacological properties.
Breast Neoplasms
[A Simple Medical Research Microdevice for Analyzing Three-dimensional Migration of Tumor Cells in Vitro].
Carcinogenesis
ATP6AP2 is Overexpressed in Breast Cancer and Promotes Breast Cancer Progression.
Carcinogenesis
BRIP1 inhibits the tumorigenic properties of cervical cancer by regulating RhoA GTPase activity.
Carcinogenesis
Bufalin inhibits glioblastoma growth by promoting proteasomal degradation of the Na+/K+-ATPase ?1 subunit.
Carcinogenesis
Integrative Transcriptomic, Proteomic and Functional Analysis Reveals ATP1B3 as a Diagnostic and Potential Therapeutic Target in Hepatocellular Carcinoma.
Carcinoma
Cardiotonic Steroids-Mediated Na+/K+-ATPase Targeting Could Circumvent Various Chemoresistance Pathways.
Carcinoma
Changes of enzyme activities recognized in lymphocytes from patients with carcinoma of the gastrointestinal tract.
Carcinoma
Copper-transporting P-type adenosine triphosphatase (ATP7B) as a cisplatin based chemoresistance marker in ovarian carcinoma: comparative analysis with expression of MDR1, MRP1, MRP2, LRP and BCRP.
Carcinoma
Copper-transporting P-type adenosine triphosphatase (ATP7B) is expressed in human gastric carcinoma.
Carcinoma
Distribution of adenosine triphosphatase in infiltrating ductal carcinoma and non-neoplastic breast.
Carcinoma
Effects of SLC31A1 and ATP7B polymorphisms on platinum resistance in patients with esophageal squamous cell carcinoma receiving neoadjuvant chemoradiotherapy.
Carcinoma
Elevated lymphocyte adenosine triphosphatase activity in patients with gastrointestinal carcinoma.
Carcinoma
Emergency Use of Targeted Osmotic Lysis for the Treatment of a Patient with Aggressive Late-Stage Squamous Cell Carcinoma of the Cervix.
Carcinoma
Enzymatic responses of transplanted tumour cells towards estrogen, progesterone and testosterone.
Carcinoma
Expression and cisplatin sensitivity of copper-transporting P-type adenosine triphosphatase (ATP7B) in human solid carcinoma cell lines.
Carcinoma
Expression of ATP7A in esophageal squamous cell carcinoma (ESCC) and its clinical significance.
Carcinoma
Expression of copper-transporting P-type adenosine triphosphatase (ATP7B) as a chemoresistance marker in human oral squamous cell carcinoma treated with cisplatin.
Carcinoma
Expression of copper-transporting P-type adenosine triphosphatase (ATP7B) as a chemoresistance marker in human solid carcinomas.
Carcinoma
Expression of copper-transporting P-type adenosine triphosphatase (ATP7B) correlates with cisplatin resistance in human non-small cell lung cancer xenografts.
Carcinoma
Expression of copper-transporting P-type adenosine triphosphatase in human esophageal carcinoma.
Carcinoma
Immunohistochemical localization of Na+, K+-ATPase in human normal and malignant pancreatic tissues.
Carcinoma
Inhibition of Na+,K+-ATPase by cisplatin and its recovery by 2-mercaptoethanol in human squamous cell carcinoma cells.
Carcinoma
Is ATP7B a predictive marker in patients with ovarian carcinoma treated with platinum-taxane combination chemotherapy?
Carcinoma
Mutation analysis of copper-transporting P-type adenosine triphosphatase (ATP7B) in human solid carcinomas.
Carcinoma
Novel progesterone target genes identified by an improved differential display technique suggest that progestin-induced growth inhibition of breast cancer cells coincides with enhancement of differentiation.
Carcinoma in Situ
Polarization of the vacuolar adenosine triphosphatase delineates a transition to high-grade pancreatic intraepithelial neoplasm lesions.
Carcinoma, Ductal
Distribution of adenosine triphosphatase in infiltrating ductal carcinoma and non-neoplastic breast.
Carcinoma, Ehrlich Tumor
A Mg2+- and Ca2+-stimulated adenosine triphosphatase at the outer surface of Ehrlich ascites tumor cells.
Carcinoma, Ehrlich Tumor
Increase in adenosine triphosphatase activity of Ehrlich ascites tumor cells following serial cultivation in media with increased (hypertonic) NaCl content.
Carcinoma, Ehrlich Tumor
Inhibition of tumor growth by an alkylation of the plasma membrane.
Carcinoma, Ehrlich Tumor
Quercetin inhibition of the induction and function of cytotoxic T lymphocytes.
Carcinoma, Hepatocellular
Adenosine triphosphatase pontin is overexpressed in hepatocellular carcinoma and coregulated with reptin through a new posttranslational mechanism.
Carcinoma, Hepatocellular
Cinobufagin Triggers Defects in Spindle Formation and Cap-Dependent Translation in Liver Cancer Cells by Inhibiting the AURKA-mTOR-eIF4E Axis.
Carcinoma, Hepatocellular
Cytochemical studies of acid phosphatase, adenosine triphosphatase and lactic dehydrogenase activity in thioacetamide-induced hepatoma.
Carcinoma, Hepatocellular
Deficiency of uncoupler-stimulated adenosine triphosphatase activity in tightly coupled hepatoma mitochondria.
Carcinoma, Hepatocellular
Effects of db-cAMP and theophylline on cell surface adenosine triphosphatase activity in cultured hepatoma cells.
Carcinoma, Hepatocellular
Expression of copper-transporting P-type adenosine triphosphatase (ATP7B) in human hepatocellular carcinoma.
Carcinoma, Hepatocellular
Mitochondrial adenosine triphosphatase of Zajdela hepatoma. III. Effect of uncouplers on the hydrolysis of intramitochondrial ATP.
Carcinoma, Hepatocellular
Mitochondrial ATPase of Zajdela hepatoma. II. Mitochondria of Zajdela hepatoma contain less adenosine triphosphatase than mitochondria of rat liver.
Carcinoma, Hepatocellular
Na+/K+-ATPase ?1 subunit, a novel therapeutic target for hepatocellular carcinoma.
Carcinoma, Hepatocellular
Na+/K+-ATPase ?3 mediates sensitivity of hepatocellular carcinoma cells to bufalin.
Carcinoma, Hepatocellular
Sodium orthovanadate overcomes sorafenib resistance of hepatocellular carcinoma cells by inhibiting Na+/K+-ATPase activity and hypoxia-inducible pathways.
Carcinoma, Hepatocellular
Uncoupler-stimulated adenosine triphosphatase activity. Deficiency in intact mitochondria from Morris hepatomas and ascites tumor cells.
Carcinoma, Non-Small-Cell Lung
Clinical outcome of cisplatin-based chemotherapy is associated with the polymorphisms of GSTP1 and XRCC1 in advanced non-small cell lung cancer patients.
Carcinoma, Non-Small-Cell Lung
Copper-transporting P-type adenosine triphosphatase (ATP7A) is associated with platinum-resistance in non-small cell lung cancer (NSCLC).
Carcinoma, Non-Small-Cell Lung
Evaluation of the relationship of erythrocyte membrane Na+/K+-ATPase enzyme activity and tumor response to chemoradiotherapy in patients diagnosed with locally advanced nonsmall cell lung cancer and glioblastoma multiforme.
Carcinoma, Non-Small-Cell Lung
Expression of copper-transporting P-type adenosine triphosphatase (ATP7B) correlates with cisplatin resistance in human non-small cell lung cancer xenografts.
Carcinoma, Non-Small-Cell Lung
MiR-495 enhances the sensitivity of non-small cell lung cancer cells to platinum by modulation of copper-transporting P-type adenosine triphosphatase A (ATP7A).
Carcinoma, Non-Small-Cell Lung
Role of sodium pump systems to determine sensitivity to mitomycin C in non-small cell lung cancer cell lines.
Carcinoma, Renal Cell
Cardiotonic Steroids-Mediated Na+/K+-ATPase Targeting Could Circumvent Various Chemoresistance Pathways.
Carcinoma, Squamous Cell
Cisplatin sensitivity of oral squamous carcinoma cells is regulated by Na+,K+-ATPase activity rather than copper-transporting P-type ATPases, ATP7A and ATP7B.
Carcinoma, Squamous Cell
Inhibition of Na+,K+-ATPase by cisplatin and its recovery by 2-mercaptoethanol in human squamous cell carcinoma cells.
Cardiomegaly
Angiotensin type 1 receptor antagonism with irbesartan inhibits ventricular hypertrophy and improves diastolic function in the remodeling post-myocardial infarction ventricle.
Cardiomegaly
Changes in sarcolemmal adenosine triphosphatase activity and in ouabain sensitivity of rat myocardium in isoproterenol-induced cardiac hypertrophy.
Cardiomegaly
Multiple signal transduction pathways link Na+/K+-ATPase to growth-related genes in cardiac myocytes. The roles of Ras and mitogen-activated protein kinases.
Cardiomegaly
Na+/K+-ATPase alpha isoforms expression in stroke-prone spontaneously hypertensive rat heart ventricles: effect of salt loading and lacidipine treatment.
Cardiomegaly
Pressure-induced cardiac hypertrophy: changes in Na+,K+-ATPase and glycoside actions in cats.
Cardiomegaly
Ral-GTPase interacts with the beta1 subunit of Na+/K+-ATPase and is activated upon inhibition of the Na+/K+ pump.
Cardiomegaly
Regulation of sarco(endo)plasmic reticulum Ca2+ adenosine triphosphatase by phospholamban and sarcolipin: implication for cardiac hypertrophy and failure.
Cardiomegaly
Studies on adenosine triphosphatase activity of rat cardiac myosin in isoproterenol-induced cardiac hypertrophy.
Cardiomyopathies
Cardiomyopathic etiology and SERCA2a reverse remodeling during mechanical support of the failing human heart.
Cardiomyopathies
Effects of acute and chronic uremia on active cation transport in rat myocardium.
Cardiomyopathies
Effects of chronic, rapid right atrial pacing on cardiac hemodynamics and myofibrillar ATPase activity in piglets.
Cardiomyopathies
Safety and efficacy of high-dose adeno-associated virus 9 encoding sarcoplasmic reticulum Ca(2+) adenosine triphosphatase delivered by molecular cardiac surgery with recirculating delivery in ovine ischemic cardiomyopathy.
Cardiomyopathies
Sarcoplasmic reticulum adenosine triphosphatase overexpression in the L-type Ca2+ channel mouse results in cardiomyopathy and Ca2+ -induced arrhythmogenesis.
Cardiomyopathies
Sodium potassium adenosine triphosphatase (Na/K-ATPase) as a therapeutic target for uremic cardiomyopathy.
Cardiomyopathies
Sodium pump and calcium channel modulation of Mg-deficiency cardiomyopathy.
Cardiomyopathy, Dilated
Human myocardial adenosine triphosphatase activities in health and heart failure.
Cardiomyopathy, Dilated
Structure and function of contractile proteins in human dilated cardiomyopathy.
Cardiomyopathy, Hypertrophic
Altered adenosine triphosphatase activities in pigs with naturally occurring hypertrophic cardiomyopathy.
Cardiotoxicity
Cardiotonic Steroids-Mediated Targeting of the Na(+)/K(+)-ATPase to Combat Chemoresistant Cancers.
Cardiotoxicity
Comparison of adriamycin- and ouabain-induced cytotoxicity and inhibition of 86rubidium transport in wild-type and ouabain-resistant C3H/10T1/2 mouse fibroblasts.
Cardiotoxicity
Molecular mechanisms of bufadienolides and their novel strategies for cancer treatment.
Cardiotoxicity
Pharmacological characterization of the activity of endogenous inotropic factor from porcine left ventricle.
Cardiotoxicity
Protective effects of dietary selenium and vitamin C in barium-induced cardiotoxicity.
Cardiovascular Diseases
Effects of obesity and estradiol on Na+/K+-ATPase and their relevance to cardiovascular diseases.
Cardiovascular Diseases
Lanatoside C Induces G2/M Cell Cycle Arrest and Suppresses Cancer Cell Growth by Attenuating MAPK, Wnt, JAK-STAT, and PI3K/AKT/mTOR Signaling Pathways.
Cardiovascular Diseases
Regulation of Na+/K+-ATPase by Estradiol and IGF-1 in Cardio-Metabolic Diseases.
Cataract
AKT activation promotes PTEN hamartoma tumor syndrome-associated cataract development.
Cataract
Extracellular matrix and Na+,K+-ATPase in human corneas following cataract surgery: comparison with bullous keratopathy and Fuchs' dystrophy corneas.
Cataract
In vitro production of steroid cataract in bovine lens. Part II: measurement of sodium-potassium adenosine triphosphatase activity.
Cataract
Lenticular rubidium uptake and plasma renin activity in weanling cataract-prone salt-sensitive rats.
Cataract
Prevention of tubulin/aldose reductase association delays the development of pathological complications in diabetic rats.
Cataract
Sodium pump inhibition and regional expression of sodium pump alpha-isoforms in lens.
Cataract
Studies on cataractogenesis in humans and in rats with alloxan-induced diabetes. I. Cation transport and sodium-potassium-dependent ATPase.
Cataract
Topical nerve growth factor attenuates streptozotocin-induced diabetic cataracts via polyol pathway inhibition and Na+/K+-ATPase upregulation.
Cerebellar Ataxia
Asparagine-905 of the mammalian phospholipid flippase ATP8A2 is essential for lipid substrate-induced activation of ATP8A2 dephosphorylation.
Cerebellar Ataxia
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.
Cerebellar Ataxia
The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management.
Cerebellar Ataxia
The Influence of Na(+), K(+)-ATPase on Glutamate Signaling in Neurodegenerative Diseases and Senescence.
Cerebral Hemorrhage
Analysis of amplicon-based NGS data from neurological disease gene panels: a new method for allele drop-out management.
Cerebral Infarction
Brain damage related to hemorrhagic transformation following cerebral ischemia and the role of K ATP channels.
Chemical and Drug Induced Liver Injury
[Biochemical mechanisms of the effect of prostaglandin E2 on the effect of parenteral nitrogenous nutrition]
Chemical and Drug Induced Liver Injury
[Effect of Arnica montana tincture on some hydrolytic enzyme activities of rat liver in experimental toxic hepatitis]
Cholecystitis
[Comparative characteristics of adenosine triphosphatase activity in the erythrocytes of patients with acute and chronic liver diseases, chronic cholecystitis and in HBs antigen carriers]
Cholera
Angiotensin II AT1 receptor/signaling mechanisms in the biphasic effect of the peptide on proximal tubular Na+,K+-ATPase.
Cholera
Experimental cholera in the rabbit intestinal loop: fluid accumulation and sodium pump inhibition.
Cholera
Sodium-potassium stimulated adenosine triphosphatase of the small intestine of man: studies in cholera and other diarrheal diseases.
Cholestasis
Assessment of Adenosine Triphosphatase Phospholipid Transporting 8B1 (ATP8B1) Function in Patients With Cholestasis With ATP8B1 Deficiency by Using Peripheral Blood Monocyte-Derived Macrophages.
Cholestasis
Effect of alpha-asarone and a derivative on lipids, bile flow and Na+/K+-ATPase in ethinyl estradiol-induced cholestasis in the rat.
Cholestasis
Intravenous fish oil emulsion attenuates total parenteral nutrition-induced cholestasis in newborn piglets.
Cholestasis
Modulation by S-adenosyl-L-methionine of hepatic Na+,K+-ATPase, membrane fluidity, and bile flow in rats with ethinyl estradiol-induced cholestasis.
Cholestasis
Role of Na+/K(+)-ATPase in Natriuretic Effect of Prolactin in a Model of Cholestasis of Pregnancy.
Cholestasis
Significant increase of Kuppfer cells associated with loss of Na+,K+-ATPase activity in rat hepatic allograft rejection.
Cholestasis
The respective roles of membrane cholesterol and of sodium potassium adenosine triphosphatase in the pathogenesis of lithocholate-induced cholestasis.
Cholestasis, Intrahepatic
Assessment of Adenosine Triphosphatase Phospholipid Transporting 8B1 (ATP8B1) Function in Patients With Cholestasis With ATP8B1 Deficiency by Using Peripheral Blood Monocyte-Derived Macrophages.
Cholestasis, Intrahepatic
Autoimmune BSEP Disease: Disease Recurrence After Liver Transplantation for Progressive Familial Intrahepatic Cholestasis.
Cholestasis, Intrahepatic
Indel in the FIC1/ATP8B1 gene-a novel rare type of mutation associated with benign recurrent intrahepatic cholestasis.
Cholestasis, Intrahepatic
Mutation Analysis and Disease Features at Presentation in a Multi-Center Cohort of Children With Monogenic Cholestasis.
Cholestasis, Intrahepatic
The Drosophila melanogaster Phospholipid Flippase dATP8B Is Required for Odorant Receptor Function.
Cholestasis, Intrahepatic
The type 4 subfamily of P-type ATPases, putative aminophospholipid translocases with a role in human disease.
Chondrosarcoma
Contribution to the knowledge of the fine structure of chondrosarcoma of bone. With a note on the localization of alkaline phosphatase and "ATPase".
Chorea
A novel ATP1A2 variant associated with severe stepwise regression, hemiplegia, epilepsy and movement disorders in two unrelated patients.
Colitis
Regional intestinal adaptations in Na+,K+-ATPase in experimental colitis and the contrasting effects of interferon-gamma.
Colonic Neoplasms
Cardiotonic Steroids-Mediated Na+/K+-ATPase Targeting Could Circumvent Various Chemoresistance Pathways.
Colonic Neoplasms
Cardiotonic Steroids-Mediated Targeting of the Na(+)/K(+)-ATPase to Combat Chemoresistant Cancers.
Colonic Neoplasms
Immunohistochemical localization of sodium-potassium-stimulated adenosine triphosphatase and carbonic anhydrase in human colon and colonic neoplasms.
Colonic Neoplasms
Polyamines secreted by cancer cells possibly account for the impairment of the human erythrocyte sodium pump activity.
Colorectal Neoplasms
FXYD6 Regulates Chemosensitivity by Mediating the Expression of Na+/K+-ATPase ?1 and Affecting Cell Autophagy and Apoptosis in Colorectal Cancer.
Colorectal Neoplasms
Interaction of Mat-8 (FXYD-3) with Na+/K+-ATPase in colorectal cancer cells.
Coma
Inhibition of rat brain Na+,K+-ATPase activity by serum from patients with fulminant hepatic failure.
Coma
Recurrent coma and fever in familial hemiplegic migraine type 2. A prospective 15-year follow-up of a large family with a novel ATP1A2 mutation.
Coma
Thermal acclimation alters Na+/K+-ATPase activity in a tissue-specific manner in Drosophila melanogaster.
Confusion
Early Treatment in Acute Severe Encephalopathy Caused by ATP1A2 Mutation of Familial Hemiplegic Migraine Type 2: Case Report and Literature Review.
Contracture
Calpain-mediated impairment of Na+/K+-ATPase activity during early reperfusion contributes to cell death after myocardial ischemia.
Contracture
Enhancement of cardiac actions of ouabain and its binding to Na+, K+-adenosine triphosphatase by increased sodium influx in isolated guinea-pig heart.
Contracture
Relationship between the potentiation of potassium-induced contracture of cardiac muscle by four cardenolides and their inhibitory effects on the sodium potassium activated adenosine triphosphatase of brain.
Contracture
Role of the sodium-calcium exchange mechanism and the effect of magnesium on sodium-free and high-potassium contractures in pregnant human myometrium.
Corneal Diseases
Human corneal endothelial cell expression of Na+,K+-adenosine triphosphatase isoforms.
Corneal Edema
Human corneal endothelial cell expression of Na+,K+-adenosine triphosphatase isoforms.
Coronary Artery Disease
Decreased Na+/K+-ATPase Activity and Altered Susceptibility to Peroxidation and Lipid Composition in the Erythrocytes of Metabolic Syndrome Patients with Coronary Artery Disease.
Coronary Artery Disease
Increased membrane lipid peroxidation and decreased Na+/K+-ATPase activity in erythrocytes of patients with stable coronary artery disease.
Cough
Selective expression of a sodium pump isozyme by cough receptors and evidence for its essential role in regulating cough.
COVID-19
Hypotheses about sub-optimal hydration in the weeks before coronavirus disease (COVID-19) as a risk factor for dying from COVID-19.
COVID-19
Na+/K+-ATPase as a Target of Cardiac Glycosides for the Treatment of SARS-CoV-2 Infection.
Craniocerebral Trauma
Exploring Neuronal Vulnerability to Head Trauma Using a Whole Exome Approach.
Craniocerebral Trauma
Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation.
Craniocerebral Trauma
The prognostic value of the brain sodium-potassium ATPase enzyme concentration in head injury.
Cystic Fibrosis
Chloride turnover and ion-transporting activities of yolk-sac preparations (yolk balls) separated from Mozambique tilapia embryos and incubated in freshwater and seawater.
Cystic Fibrosis
Cortisol regulates insulin-like growth-factor binding protein (igfbp) gene expression in Atlantic salmon parr.
Cystic Fibrosis
Dynamics of Gene Expression Responses for Ion Transport Proteins and Aquaporins in the Gill of a Euryhaline Pupfish during Freshwater and High-Salinity Acclimation.
Cystic Fibrosis
Functional classification of mitochondrion-rich cells in euryhaline Mozambique tilapia (Oreochromis mossambicus) embryos, by means of triple immunofluorescence staining for Na+/K+-ATPase, Na+/K+/2Cl- cotransporter and CFTR anion channel.
Cystic Fibrosis
Gene expression after freshwater transfer in gills and opercular epithelia of killifish: insight into divergent mechanisms of ion transport.
Cystic Fibrosis
Genome-wide analysis of MicroRNA-messenger RNA interactome in ex-vivo gill filaments, Anguilla japonica.
Cystic Fibrosis
Influence of salinity on the localization of Na+/K+-ATPase, Na+/K+/2Cl- cotransporter (NKCC) and CFTR anion channel in chloride cells of the Hawaiian goby (Stenogobius hawaiiensis).
Cystic Fibrosis
Regulation of Cl- Electrolyte Permeability in Epithelia by Active Traditional Chinese Medicine Monomers for Diarrhea.
Cystic Fibrosis
Short- and long-term low-salinity acclimation effects on the branchial and intestinal gene expression in the European seabass (Dicentrarchus labrax).
Cystic Fibrosis
Systemic versus tissue-level prolactin signaling in a teleost during a tidal cycle.
Cystic Fibrosis
The effect of environmental salinity on the protein expression of Na+/K+-ATPase, Na+/K+/2Cl- cotransporter, cystic fibrosis transmembrane conductance regulator, anion exchanger 1, and chloride channel 3 in gills of a euryhaline teleost, Tetraodon nigroviridis.
Cystic Fibrosis
The effects of transfer from steady-state to tidally-changing salinities on plasma and branchial osmoregulatory variables in adult Mozambique tilapia.
Cysts
A role for Na/K adenosine triphosphatase in the pathogenesis of cyst formation in experimental polycystic kidney disease.
Cysts
Congenital murine polycystic kidney disease. II. Pathogenesis of tubular cyst formation.
Cysts
Effect of antihydatid drugs on carbohydrate metabolism of metacestode of echinococcus granulosus.
Cysts
Effects of mebendazole, albendazole, and praziquantel on alkaline phosphatase, acid phosphatase, and adenosine triphosphatase of Echinococcus granulosus cysts harbored in mice.
Cysts
Sarcocystis fusiformis: some Krebs cycle enzymes in various fractions of sarcocysts of buffalo (Bubalus bubalis).
Cysts
Triiodothyronine-induced cyst formation in metanephric organ culture: the role of increased Na-K-adenosine triphosphatase activity.
Cysts
[Seasonal changes in the adenosine triphosphatase activity in the germinal cysts of the testis of the common frog Rana temporaria. An enzyme histochemical study]
Cysts
[Ultrastructural localization of alkaline phosphatase and ATP-ase in cyst stages of Sarcocystis tenella (Sporozoa, Coccidia) parasitic in the esophagus of sheep (author's transl)]
Cytochrome-c Oxidase Deficiency
Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implications.
Deficiency Diseases
Menkes disease diagnosed by a novel ATP7A frameshift mutation in a patient with infantile spasms-a case report.
Dehydration
An hypothesis on the consolidation and PGE1-induced deconsolidation of a platelet plug.
Dehydration
Solute effects on the sodium pump. An evaluation of the osmotic dehydration hypothesis.
Dementia
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase.
Demyelinating Diseases
Potential implications of Helicobacter pylori-related neutrophil-activating protein.
Demyelinating Diseases
Quercetin treatment regulates the Na+,K+-ATPase activity, peripheral cholinergic enzymes, and oxidative stress in a rat model of demyelination.
Dengue
NS3 helicase from dengue virus specifically recognizes viral RNA sequence to ensure optimal replication.
Diabetes Complications
Aldose reductase and its inhibition in the control of diabetic complications.
Diabetes Complications
Modifications induced by diabetes on the physicochemical and functional properties of erythrocyte plasma membrane.
Diabetes Complications
NO levels in diabetes mellitus: Effects of l-NAME and insulin on LCAT, Na(+)/K(+) ATPase activity and lipid profile.
Diabetes Mellitus
Effects of proinsulin C-peptide on nitric oxide, microvascular blood flow and erythrocyte Na+,K+-ATPase activity in diabetes mellitus type I.
Diabetes Mellitus
Endogenous sodium pump inhibitors, diabetes mellitus and preeclampsia Preliminary observations and a hypothesis.
Diabetes Mellitus
Impairment of sodium pump and Na/H exchanger in erythrocytes from non-insulin dependent diabetes mellitus patients: effect of tea catechins.
Diabetes Mellitus
NO levels in diabetes mellitus: Effects of l-NAME and insulin on LCAT, Na(+)/K(+) ATPase activity and lipid profile.
Diabetes Mellitus
Prevention of tubulin/aldose reductase association delays the development of pathological complications in diabetic rats.
Diabetes Mellitus
Small intestinal Na+,K+-adenosine triphosphatase activity and gene expression in experimental diabetes mellitus.
Diabetes Mellitus
Sorbitol, myo-inositol and sodium-potassium ATPase in diabetic peripheral nerve.
Diabetes Mellitus
[Tian-shou liquor on activity of cell membrane and energy metabolism in diabetes mellitus]
Diabetes Mellitus, Experimental
Abnormal membrane fluidity and acetylcholinesterase activity in erythrocytes from insulin-dependent diabetic patients.
Diabetes Mellitus, Experimental
Effects of streptozotocin diabetes and insulin treatment on myocardial sodium pump and contractility of the rat heart.
Diabetes Mellitus, Experimental
Impaired rat sciatic nerve sodium-potassium adenosine triphosphatase in acute streptozocin diabetes and its correction by dietary myo-inositol supplementation.
Diabetes Mellitus, Experimental
Na+,K+-ATPase and Mg2+-ATPase activities in different regions of rat brain during alloxan diabetes.
Diabetes Mellitus, Experimental
Reduced glomerular sodium/potassium adenosine triphosphatase activity in acute streptozocin diabetes and its prevention by oral sorbinil.
Diabetes Mellitus, Type 1
A study on human umbilical cord endothelial cells: functional modifications induced by plasma from insulin-dependent diabetes mellitus patients.
Diabetes Mellitus, Type 1
Influence of low density lipoprotein from insulin-dependent diabetic patients on platelet functions.
Diabetes Mellitus, Type 1
Modifications induced by insulin-dependent diabetes mellitus on human placental Na+/K+-adenosine triphosphatase.
Diabetes Mellitus, Type 1
Regulation of the inducible nitric oxide synthase and sodium pump in type 1 diabetes.
Diabetes Mellitus, Type 1
Sialic acid, diabetes, and aging: a study on the erythrocyte membrane.
Diabetes Mellitus, Type 2
Association of sick sinus syndrome with hyperinsulinemia and insulin resistance in patients with non-insulin-dependent diabetes mellitus: report of four cases.
Diabetes Mellitus, Type 2
Reduction of erythrocyte (Na(+)-K+) ATPase activities in non-insulin-dependent diabetic patients with hyperkalemia.
Diabetes Mellitus, Type 2
Sialic acid, diabetes, and aging: a study on the erythrocyte membrane.
Diabetic Neuropathies
Accumulation of sorbitol in the sciatic nerve modulates circadian properties of diabetes-induced neuropathic pain hypersensitivity in a diabetic mouse model.
Diabetic Neuropathies
Effect of pre-germinated brown rice intake on diabetic neuropathy in streptozotocin-induced diabetic rats.
Diabetic Neuropathies
Endoneurial ATPase activity in Tangier disease and other peripheral neuropathies.
Diabetic Neuropathies
Erythropoietin: A potential drug in the management of diabetic neuropathy.
Diabetic Neuropathies
Genetic and environmental regulation of Na/K adenosine triphosphatase activity in diabetic patients.
Diabetic Neuropathies
Metabolic correction in the management of diabetic peripheral neuropathy: improving clinical results beyond symptom control.
Diabetic Neuropathies
Platelet sodium and potassium ATPase [corrected] activity and noradrenaline efflux rate in relation to autonomic and peripheral nerve function in insulin-dependent diabetic patients.
Drug Resistant Epilepsy
A novel ATP1A2 variant associated with severe stepwise regression, hemiplegia, epilepsy and movement disorders in two unrelated patients.
Duodenal Ulcer
[Prognostic factors of the speed of cicatrization in duodenal ulcer. Controlled trial of omeprazole versus ranitidine]
Dystonia
A novel ATP1A2 variant associated with severe stepwise regression, hemiplegia, epilepsy and movement disorders in two unrelated patients.
Dystonia
Abnormal high-frequency burst firing of cerebellar neurons in rapid-onset dystonia-parkinsonism.
Dystonia
Cellular function and pathological role of ATP13A2 and related P-type transport ATPases in Parkinson's disease and other neurological disorders.
Dystonia
Genome-wide screen for modifiers of Na + /K + ATPase alleles identifies critical genetic loci.
Dystonia
Hypothermia-induced dystonia and abnormal cerebellar activity in a mouse model with a single disease-mutation in the sodium-potassium pump.
Dystonia
Mutations Phe785Leu and Thr618Met in Na+,K+-ATPase, associated with familial rapid-onset dystonia parkinsonism, interfere with Na+ interaction by distinct mechanisms.
Dystonia
Rescue of Na+ Affinity in Aspartate-928 Mutants of Na+,K+-ATPase by Secondary Mutation of Glutamate-314.
Dystonia
The structure of the Na+,K+-ATPase and mapping of isoform differences and disease-related mutations.
Dystonic Disorders
Striatal dopaminergic dysregulation and dystonia-like movements induced by sensorimotor stress in a pharmacological mouse model of rapid-onset dystonia-parkinsonism.
Eczema
[Adenosine triphosphoric acid content and adenosine triphosphatase activity in eczema]
Embolism
Microsphere embolism-induced changes in noradrenaline uptake of the cerebral cortex in rats.
Encephalitis, Tick-Borne
[Change in Na+,K+-ATPase activity during reproduction of the tick-borne encephalitis virus in SPEV cell culture]
Encephalomyelitis, Autoimmune, Experimental
Localization of adenosine triphosphatase activity of the endothelia in chronic relapsing experimental allergic encephalomyelitis.
Endolymphatic Hydrops
Na+,K+-ATPase and Ca2+-ATPase activities in the cochlear lateral wall following surgical induction of hydrops.
Endometrial Neoplasms
Expression of copper-transporting P-type adenosine triphosphatase (ATP7B) as a prognostic factor in human endometrial carcinoma.
Eosinophilic Granuloma
Langerhans' cells and macrophages in eosinophilic granuloma. An enzyme-histochemical, enzyme-cytochemical, and ultrastructural study.
Epilepsies, Partial
Astroglial contribution in human temporal lobe epilepsy: K+ activation of Na+,K+-ATPase in bulk isolated glial cells and synaptosomes.
Epilepsy
A Novel ATP1A2 Gene Variant Associated With Pure Sporadic Hemiplegic Migraine Improved After Patent Foramen Ovale Closure: A Case Report.
Epilepsy
A novel ATP1A2 variant associated with severe stepwise regression, hemiplegia, epilepsy and movement disorders in two unrelated patients.
Epilepsy
An Infant With Epilepsy and Recurrent Hemiplegia due to Compound Heterozygous Variants in ATP1A2.
Epilepsy
Analysis of chromosome 1 microsatellite markers and the FHM2-ATP1A2 gene mutations in migraine pedigrees.
Epilepsy
Astroglial contribution in human temporal lobe epilepsy: K+ activation of Na+,K+-ATPase in bulk isolated glial cells and synaptosomes.
Epilepsy
Biphasic neurovascular changes in prolonged migraine aura in familial hemiplegic migraine type 2.
Epilepsy
Characteristics of cortical spreading depression and c-Fos expression in transgenic mice having a mutation associated with familial hemiplegic migraine 2.
Epilepsy
Early onset severe ATP1A2 epileptic encephalopathy: Clinical characteristics and underlying mutations.
Epilepsy
Familial Hemiplegic Migraine With Asymmetric Encephalopathy Secondary to ATP1A2 Mutation: A Case Series.
Epilepsy
Functional characterization of a novel C-terminal ATP1A2 mutation causing hemiplegic migraine and epilepsy.
Epilepsy
Functional correlation of ATP1A2 mutations with phenotypic spectrum: from pure hemiplegic migraine to its variant forms.
Epilepsy
Genetic effects of ATP1A2 in familial hemiplegic migraine type II and animal models.
Epilepsy
In vitro studies of the influence of glutamatergic agonists on the Na+,K+-ATPase and K+-p-nitrophenylphosphatase activities in the hippocampus and frontal cortex of rats.
Epilepsy
Kinetic alterations due to a missense mutation in the Na,K-ATPase alpha2 subunit cause familial hemiplegic migraine type 2.
Epilepsy
Migraine and epilepsy: A focus on overlapping clinical, pathophysiological, molecular, and therapeutic aspects.
Epilepsy
Neural dysfunction and neurodegeneration in Drosophila Na+/K+ ATPase alpha subunit mutants.
Epilepsy
Neurovascular changes in prolonged migraine aura in FHM with a novel ATP1A2 gene mutation.
Epilepsy
Opening of the blood-brain barrier preceding cortical edema in a severe attack of FHM type II.
Epilepsy
Prophylactically administered phenytoin. Effects on the development of chronic cobalt-induced epilepsy in the cat.
Epilepsy
Regional distributions of hippocampal Na+,K(+)-ATPase, cytochrome oxidase, and total protein in temporal lobe epilepsy.
Epilepsy
Relationship between susceptibility to DMCM-induced generalized motor convulsions and low-affinity [3H]-ouabain binding in membranes in rat brain.
Epilepsy
Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutation.
Epilepsy
The CACNA1A and ATP1A2 genes are not involved in dominantly inherited migraine with aura.
Epilepsy
The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families.
Epilepsy
The kinetics of non-synaptically triggered acute excitotoxic responses in the central nervous system observed using intrinsic optical signals.
Epilepsy, Benign Neonatal
Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions.
Epilepsy, Generalized
Common variants of ATP1A3 but not ATP1A2 are associated with Chinese genetic generalized epilepsies.
Epilepsy, Temporal Lobe
Astroglial contribution in human temporal lobe epilepsy: K+ activation of Na+,K+-ATPase in bulk isolated glial cells and synaptosomes.
Epilepsy, Temporal Lobe
Regional distributions of hippocampal Na+,K(+)-ATPase, cytochrome oxidase, and total protein in temporal lobe epilepsy.
Esophageal Squamous Cell Carcinoma
Effects of SLC31A1 and ATP7B polymorphisms on platinum resistance in patients with esophageal squamous cell carcinoma receiving neoadjuvant chemoradiotherapy.
Esophageal Squamous Cell Carcinoma
Expression of ATP7A in esophageal squamous cell carcinoma (ESCC) and its clinical significance.
Esophagitis
Regulation of Na/H exchanger-1 in gastroesophageal reflux disease: possible interaction of histamine receptor.
Essential Hypertension
A plasma inhibitor of sodium and potassium activated adenosine triphosphatase in patients with essential hypertension.
Essential Hypertension
Abnormal leucocyte sodium transport in Chinese patients with essential hypertension and their normotensive offsprings.
Essential Hypertension
An increase in a circulating inhibitor of Na+,K+-dependent ATPase: a possible link between salt intake and the development of essential hypertension.
Essential Hypertension
Assay of a circulating sodium pump inhibitor in patients with essential hypertension and normotensive subjects.
Essential Hypertension
Blood pressure in essential hypertension correlates with the concentration of a circulating inhibitor of the sodium pump.
Essential Hypertension
Digibind Reverses Inhibition of Cellular rb+ Uptake Caused by Endogenous Sodium Pump Inhibitors Present in Serum and Placenta of Women With Preeclampsia.
Essential Hypertension
Digitalis-like factor and digoxin-like immunoreactive factor in diabetic women with preeclampsia, transient hypertension of pregnancy, and normotensive pregnancy.
Essential Hypertension
Effect of the calcium antagonist verapamil on human leucocyte sodium transport in vitro.
Essential Hypertension
Effects of changes in dietary sodium intake on normotensive subjects with and without a genetic predisposition to essential hypertension.
Essential Hypertension
Effects of lead and a low-molecular-weight endogenous plasma inhibitor on the kinetics of sodium-potassium-activated adenosine triphosphatase and potassium-activated p-nitrophenylphosphatase.
Essential Hypertension
Erythrocyte and plasma Ca2+, Mg2+ and cell membrane adenosine triphosphatase activity in patients with essential hypertension.
Essential Hypertension
Erythrocyte calcium-stimulated, magnesium-activated adenosine 5'-triphosphatase activity in essential hypertension.
Essential Hypertension
Erythrocyte membrane ouabain-sensitive Na+, K(+)-ATPase of hypertensive Nigerians.
Essential Hypertension
Forearm vasoconstrictor response to ouabain: studies in patients with mild and moderate essential hypertension.
Essential Hypertension
Genetic and ethnic influences on the distribution of sodium and potassium in normotensive and hypertensive subjects.
Essential Hypertension
Humoral sodium transport inhibitor in acute volume expansion and low renin hypertension.
Essential Hypertension
Increased concentrations of a circulating sodium pump inhibitor in essential hypertension and uraemia and its partial purification from haemofiltrate.
Essential Hypertension
Kinetics of the human leucocyte Na(+)-H+ antiport in essential hypertension.
Essential Hypertension
Low-concentration ouabain does not inhibit noradrenaline-induced contraction of human resistance arteries.
Essential Hypertension
Maximum binding of ouabain to erythrocytes in relation to a family history of essential hypertension, sodium balance and body weight in normotensive children.
Essential Hypertension
Measurement by bioluminescence technique of erythrocyte membrane Na+,K+-ATPase activity in hypertensive patients.
Essential Hypertension
Observations on the "cascade" of Na-K-ATPase inhibitory and digoxin-like immunoreactive material in human urine: possible relevance to essential hypertension.
Essential Hypertension
Ouabain-like and non-ouabain-like factors in plasma of patients with essential hypertension.
Essential Hypertension
Ouabainlike Na+,K+-ATPase inhibitor in the plasma of normotensive and hypertensive humans and rats.
Essential Hypertension
Partial purification and properties of a plasma ouabain-like inhibitor of Na+, K+-ATPase in patients with essential hypertension.
Essential Hypertension
Plasma sodium pump inhibitor in essential hypertension and normotensive subjects with hypertensive heredity.
Essential Hypertension
Platelet and erythrocyte Mg2+, Ca2+, Na+, K+ and cell membrane adenosine triphosphatase activity in essential hypertension in blacks.
Essential Hypertension
Predominance of high molecular weight plasma Na(+)-K(+)-ATPase inhibitor in essential hypertension.
Essential Hypertension
Raised sodium pump activity and a circulating sodium transport inhibitor demonstrated on red blood cells of patients with untreated essential hypertension: correlation of pump activity with potassium permeability.
Essential Hypertension
Red blood cell Na+,K+-ATPase in men with newly diagnosed or previously treated essential hypertension.
Essential Hypertension
Reduced number of erythrocyte sodium pump units in essential hypertension.
Essential Hypertension
Regulation of sodium/potassium ATPase activity: impact on salt balance and vascular contractility.
Essential Hypertension
Relation of sodium-potassium adenosine triphosphatase inhibitor to sympathetic nervous system during salt-loading in essential hypertension.
Essential Hypertension
Relationship between the sympathetic nervous system and sodium potassium adenosine triphosphatase inhibitor in salt-sensitive patients with essential hypertension.
Essential Hypertension
Role of a natriuretic factor in essential hypertension: an hypothesis.
Essential Hypertension
Sodium pump inhibitor in the serum of patients with essential hypertension and its partial purification from hemofiltrate.
Essential Hypertension
The effect of ouabain on pressor responses to infused noradrenaline in patients with essential hypertension.
Essential Hypertension
The role of a humoral Na+,K+-ATPase inhibitor in regulating precapillary vessel tone.
Essential Hypertension
The sodium pump and energy regulation: some new aspects for essential hypertension, diabetes II and severe overweight.
Essential Hypertension
[Association of the polymorphisms of sodium transport related genes with essential hypertension]
Essential Hypertension
[Comparison of extra renal potassium management in hypertensive, diabetic and normal subjects]
Facial Paralysis
Impaired Ranvier node sodium-potassium adenosine triphosphatase may induce facial palsy.
Foramen Ovale, Patent
A Novel ATP1A2 Gene Variant Associated With Pure Sporadic Hemiplegic Migraine Improved After Patent Foramen Ovale Closure: A Case Report.
Friedreich Ataxia
Specificity of biophysical and biochemical alterations in erythrocyte membranes in neurological disorders--Huntington's disease, Friedreich's ataxia, Alzheimer's disease, amyotrophic lateral sclerosis, and myotonic and duchenne muscular dystrophy.
galactokinase deficiency
Suckling rat brain regional distribution of Na+,K+-atpase activity in the in vitro galactosaemia: the effect of L-cysteine and glutathione.
Galactosemias
Suckling rat brain regional distribution of Na+,K+-atpase activity in the in vitro galactosaemia: the effect of L-cysteine and glutathione.
Gallstones
Evidence for oxidative stress in the gall bladder mucosa of gall stone patients.
Gangliosidoses
Fluorescence polarization analysis, lipid composition, and Na+, K+-ATPase kinetics of synaptosomal membranes in feline GM1 and GM2 gangliosidosis.
Gangliosidosis, GM1
Fluorescence polarization analysis, lipid composition, and Na+, K+-ATPase kinetics of synaptosomal membranes in feline GM1 and GM2 gangliosidosis.
Gastritis
Analysis of mononuclear cell infiltrate and cytokine production in murine autoimmune gastritis.
Gastritis
Interleukin 27 Protects From Gastric Atrophy and Metaplasia During Chronic Autoimmune Gastritis.
Gastritis
Monoclonal antibodies specific for the core protein of the beta-subunit of the gastric proton pump (H+/K+ ATPase). An autoantigen targetted in pernicious anaemia.
Gastritis, Atrophic
Variations of energy metabolism and adenosine triphosphatase activity in gastric mucosa in chronic atrophic gastritis rats with Qi deficiency and blood stasis syndrome and effect of zhiweifangbian capsule.
Gastroenteritis
Natural cardenolides suppress coronaviral replication by downregulating JAK1 via a Na+/K+-ATPase independent proteolysise.
Gastroenteritis
The cardenolide ouabain suppresses coronaviral replication via augmenting a Na+/K+-ATPase-dependent PI3K_PDK1 axis signaling.
Gastroesophageal Reflux
Regulation of Na/H exchanger-1 in gastroesophageal reflux disease: possible interaction of histamine receptor.
Genetic Diseases, Inborn
Mitochondrial G8292A and C8794T mutations in patients with Niemann-Pick disease type C.
Glioblastoma
Bufalin inhibits glioblastoma growth by promoting proteasomal degradation of the Na+/K+-ATPase ?1 subunit.
Glioblastoma
Cardiotonic Steroids-Mediated Targeting of the Na(+)/K(+)-ATPase to Combat Chemoresistant Cancers.
Glioblastoma
Editorial: on the road to multi-modal and pluri-disciplinary treatment of glioblastomas.
Glioblastoma
Epi-reevesioside F inhibits Na+/K+-ATPase, causing cytosolic acidification, Bak activation and apoptosis in glioblastoma.
Glioblastoma
Evaluation of the relationship of erythrocyte membrane Na+/K+-ATPase enzyme activity and tumor response to chemoradiotherapy in patients diagnosed with locally advanced nonsmall cell lung cancer and glioblastoma multiforme.
Glioblastoma
Inhibition of Na+/K+-ATPase induces hybrid cell death and enhanced sensitivity to chemotherapy in human glioblastoma cells.
Glioblastoma
Present and potential future adjuvant issues in high-grade astrocytic glioma treatment.
Glioblastoma
Response of sodium pump to ouabain challenge in human glioblastoma cells in culture.
Glioblastoma
Spider venom components decrease glioblastoma cell migration and invasion through RhoA-ROCK and Na+/K+-ATPase ?2: potential molecular entities to treat invasive brain cancer.
Glioblastoma
Targeting ?2 subunit of Na+/K+-ATPase induces glioblastoma cell apoptosis through elevation of intracellular Ca2.
Glioblastoma
Targeting the alpha 1 subunit of the sodium pump to combat glioblastoma cells.
Glioblastoma
The sodium pump ?1 subunit regulates bufalin sensitivity of human glioblastoma cells through the p53 signaling pathway.
Glioblastoma
The sodium pump alpha1 subunit as a potential target to combat apoptosis-resistant glioblastomas.
Glioblastoma
Update on the effects of the sodium pump ?1 subunit on human glioblastoma: from the laboratory to the clinic.
Glioma
Alterations of membrane integrity and cellular constituents by arachidonic acid in neuroblastoma and glioma cells.
Glioma
ATP1A1 Integrates AKT and ERK Signaling via Potential Interaction With Src to Promote Growth and Survival in Glioma Stem Cells.
Glioma
Cardiotonic Steroids-Mediated Na+/K+-ATPase Targeting Could Circumvent Various Chemoresistance Pathways.
Glioma
Marinobufagenin inhibits glioma growth through sodium pump ?1 subunit and ERK signaling-mediated mitochondrial apoptotic pathway.
Glioma
Present and potential future adjuvant issues in high-grade astrocytic glioma treatment.
Glioma
The sodium pump ?1 subunit regulates bufalin sensitivity of human glioblastoma cells through the p53 signaling pathway.
Glioma
The sodium pump alpha1 subunit as a potential target to combat apoptosis-resistant glioblastomas.
Glioma
[Distribution of adenosine triphosphatase activity in the culture of cerebral gliomas]
Glomerulonephritis
Glomerulonephritis and sodium retention: enhancement of Na+/K+-ATPase activity in the collecting duct is shared by rats with puromycin induced nephrotic syndrome and mice with spontaneous lupus-like glomerulonephritis.
Glomerulonephritis
[Adenosine triphosphatase activity of erythrocytes in diffuse glomerulonephritis in children]
glucose-6-phosphatase deficiency
Induction of altered hepatic foci in rats by the administration of hypolipidemic peroxisome proliferators alone or following a single dose of diethylnitrosamine.
Glycogen Storage Disease Type I
Induction of altered hepatic foci in rats by the administration of hypolipidemic peroxisome proliferators alone or following a single dose of diethylnitrosamine.
Granuloma
Susceptibility of desert sheep to infection with Schistosoma mansoni of Northern Sudan.
Graves Disease
[Therapeutic effect and its mechanism exploration on mainly using traditional Chinese medicine of replenishing qi and nourishing yin in treating Graves disease]
Head and Neck Neoplasms
[The cytochemical determination of alpha-glycerophosphate dehydrogenase and adenosine triphosphatase in the peripheral blood lymphocytes of patients with hepatobiliary system pathology]
Hearing Loss
A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraine.
Hearing Loss
The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management.
Hearing Loss
The Drosophila melanogaster Phospholipid Flippase dATP8B Is Required for Odorant Receptor Function.
Hearing Loss
The Endocannabinoid/Cannabinoid Receptor 2 System Protects Against Cisplatin-Induced Hearing Loss.
Hearing Loss, Sensorineural
A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraine.
Hearing Loss, Sensorineural
Functional consequences of the CAPOS mutation E818K of Na+,K+-ATPase.
Hearing Loss, Sensorineural
Inhibition of Na+,K+-stimulated ATPase in the cochlea of the guinea pig. A potential cause of disturbed inner ear function in terminal renal failure.
Hearing Loss, Sensorineural
The Influence of Na(+), K(+)-ATPase on Glutamate Signaling in Neurodegenerative Diseases and Senescence.
Heart Defects, Congenital
Sodium pump reduction correlates with aortic clamp time in pediatric heart surgery.
Heart Diseases
Insect Collections as an Untapped Source of Bioactive Compounds-Fireflies (Coleoptera: Lampyridae) and Cardiotonic Steroids as a Proof of Concept.
Heart Failure
Altered diastolic [Ca2+]i handling in human ventricular myocytes from patients with terminal heart failure.
Heart Failure
Altered Na+/Ca2+-exchanger activity due to downregulation of Na+/K+-ATPase {alpha}2-isoform in heart failure.
Heart Failure
Altered sarco(endo)plasmic reticulum calcium adenosine triphosphatase 2a content: Targets for heart failure therapy.
Heart Failure
Antiherpes activity of glucoevatromonoside, a cardenolide isolated from a Brazilian cultivar of Digitalis lanata.
Heart Failure
Assist devices fail to reverse patterns of fetal gene expression despite beta-blockers.
Heart Failure
Association of chronic congestive heart failure in humans with an intrinsic upregulation in skeletal muscle sarcoplasmic reticulum calcium ion adenosine triphosphatase activity.
Heart Failure
Association of depressed myofibrillar adenosine triphosphatase and reduced contractility in experimental heart failure.
Heart Failure
Cardiac glycoside bufalin blocks cancer cell growth by inhibition of Aurora A and Aurora B activation via PI3K-Akt pathway.
Heart Failure
Cardiac Glycosides Activate the Tumor Suppressor and Viral Restriction Factor Promyelocytic Leukemia Protein (PML).
Heart Failure
Cardiac Resynchronization and Circulating Markers of Sarcoplasmic Reticulum Calcium Handling and Sudden Death Risk.
Heart Failure
Cardiotonic steroid ouabain stimulates steroidogenesis in Leydig cells via the ?3 isoform of the sodium pump.
Heart Failure
Comparison of heart sarcolemmal enzyme activities in normal and cardiomyopathic (UM-X7.1) hamsters.
Heart Failure
Digitoxin-induced cytotoxicity in cancer cells is mediated through distinct kinase and interferon signalling networks.
Heart Failure
Distribution of sodium and potassium in chronic obstructive pulmonary disease.
Heart Failure
Human myocardial adenosine triphosphatase activities in health and heart failure.
Heart Failure
Isoform-specific alterations in cardiac and erythrocyte Na+,K+-ATPase activity induced by norepinephrine.
Heart Failure
Istaroxime, a stimulator of sarcoplasmic reticulum calcium adenosine triphosphatase isoform 2a activity, as a novel therapeutic approach to heart failure.
Heart Failure
Magnesium treatment of diuretic-induced hyponatremia with a preliminary report of a new aldosterone-antagonist.
Heart Failure
Marinobufagenin, an endogenous ligand of alpha-1 sodium pump, is a marker of congestive heart failure severity.
Heart Failure
Mitigation of myocardial fibrosis by molecular cardiac surgery-mediated gene overexpression.
Heart Failure
Ouabain potentiates the antimicrobial activity of aminoglycosides against Staphylococcus aureus.
Heart Failure
Reduced sodium pump alpha1, alpha3, and beta1-isoform protein levels and Na+,K+-ATPase activity but unchanged Na+-Ca2+ exchanger protein levels in human heart failure.
Heart Failure
Regulation of Na+/K+-ATPase by Estradiol and IGF-1 in Cardio-Metabolic Diseases.
Heart Failure
Role of inositol 1,4,5-trisphosphate receptors in regulating apoptotic signaling and heart failure.
Heart Failure
The ?2-isoform of the Na+/K+-ATPase protects against pathological remodeling and ?-adrenergic desensitization after myocardial infarction.
Heart Failure
The amino acid composition of actin and myosin and Ca2+-activated myosin adenosine triphosphatase in chronic canine congestive heart failure.
Heart Failure
The cardiac glycoside ouabain activates NLRP3 inflammasomes and promotes cardiac inflammation and dysfunction.
Heart Failure
[Cancer cell-specific functional relation between Na+,K+-ATPase and volume-regulated anion channel].
Hemiplegia
'Absence of T378N mutation of ATP1A2 gene in five patients with alternating hemiplegia of childhood'.
Hemiplegia
A novel ATP1A2 variant associated with severe stepwise regression, hemiplegia, epilepsy and movement disorders in two unrelated patients.
Hemiplegia
A novel lethal recognizable polymicrogyric syndrome caused by ATP1A2 homozygous truncating variants.
Hemiplegia
Alternating hemiplegia of childhood and a pathogenic variant of ATP1A3: a case report and pathophysiological considerations.
Hemiplegia
Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation.
Hemiplegia
Alternating hemiplegia of childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2.
Hemiplegia
An Infant With Epilepsy and Recurrent Hemiplegia due to Compound Heterozygous Variants in ATP1A2.
Hemiplegia
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.
Hemiplegia
Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations.
Hemiplegia
CACNA1A-Linked Hemiplegic Migraine in GLUT 1 Deficiency Syndrome: A Case Report.
Hemiplegia
Characterization of cognitive deficits in mice with an alternating hemiplegia-linked mutation.
Hemiplegia
Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severity.
Hemiplegia
De novo ATP1A2 variants in two Chinese children with alternating hemiplegia of childhood upgraded the gene-disease relationship and variant classification: a case report.
Hemiplegia
Genome-wide screen for modifiers of Na + /K + ATPase alleles identifies critical genetic loci.
Hemiplegia
Hypothermia-induced dystonia and abnormal cerebellar activity in a mouse model with a single disease-mutation in the sodium-potassium pump.
Hemiplegia
Knock-in mouse model of alternating hemiplegia of childhood: behavioral and electrophysiologic characterization.
Hemiplegia
Rescue of Na+ Affinity in Aspartate-928 Mutants of Na+,K+-ATPase by Secondary Mutation of Glutamate-314.
Hemiplegia
The Influence of Na(+), K(+)-ATPase on Glutamate Signaling in Neurodegenerative Diseases and Senescence.
Hemoglobinuria
[Activity of adenosine triphosphatase of the erythrocytic membrane in paroxysmal nacturnal hemoglobinuria]
Hepatic Encephalopathy
Inhibition of rat brain Na+,K+-ATPase activity by serum from patients with fulminant hepatic failure.
Hepatitis
[Histochemical studies of the effect of Meritschleri mineral water on the activity of lipase, cytochrome oxidase and adenosine triphosphatase enzymes in the liver in experimental hepatitis]
Hepatitis
[Lactate dehydrogenase, glucosephosphate dehydrogenase, glutathione reductase and adenosine triphosphatase activities in the erythrocytes of patients with acute viral hepatitis]
Hepatitis
[The activities of acid phosphatase (ACP) and Mg++ adenosine triphosphatase in acute hepatitis with submassive necrosis]
Hepatitis
[The cytochemical determination of alpha-glycerophosphate dehydrogenase and adenosine triphosphatase in the peripheral blood lymphocytes of patients with hepatobiliary system pathology]
Hepatitis B
Immune and enzyme histochemical studies of a human hepatocellular carcinoma cell line producing hepatitis B surface antigen.
Hepatitis C
Antigenicity of a recombinant NS3 protein representative of ATPase/helicase domain from hepatitis C virus.
Hepatolenticular Degeneration
A new mutation of Wilson's disease P-type ATPase gene in a patient with cirrhosis and coombs-positive hemolytic anemia.
Hepatolenticular Degeneration
Adenosine triphosphate-dependent copper transport in human liver.
Hepatolenticular Degeneration
Adenosine triphosphate-dependent copper transport in isolated rat liver plasma membranes.
Hepatolenticular Degeneration
Concordance rates of Wilson's disease phenotype among siblings.
Hepatolenticular Degeneration
Copper-dependent interaction of dynactin subunit p62 with the N terminus of ATP7B but not ATP7A.
Hepatolenticular Degeneration
Copper-induced apical trafficking of ATP7B in polarized hepatoma cells provides a mechanism for biliary copper excretion.
Hepatolenticular Degeneration
Developmental expression of Commd1 in the liver of the Jackson toxic milk mouse.
Hepatolenticular Degeneration
Direct sequencing of mutations in the copper-transporting P-type adenosine triphosphate (ATP7B) gene for diagnosis and pathogenesis of Wilson's disease.
Hepatolenticular Degeneration
Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B.
Hepatolenticular Degeneration
Disturbed copper transport in humans. Part 2: mutations of the ATP7B gene lead to Wilson disease (WD).
Hepatolenticular Degeneration
Diverse Functional Properties of Wilson Disease ATP7B Variants.
Hepatolenticular Degeneration
Efficacy of zinc supplementation in preventing acute hepatitis in Long-Evans Cinnamon rats.
Hepatolenticular Degeneration
Gene mutations in Wilson disease in Egyptian children: report on two novel mutations.
Hepatolenticular Degeneration
Genetic analysis of BIRC4/XIAP as a putative modifier gene of Wilson disease.
Hepatolenticular Degeneration
Genetically confirmed Wilson disease in a 9-month old boy with elevations of aminotransferases.
Hepatolenticular Degeneration
High yield heterologous expression of wild-type and mutant Cu+-ATPase (ATP7B, Wilson disease protein) for functional characterization of catalytic activity and serine residues undergoing copper-dependent phosphorylation.
Hepatolenticular Degeneration
Identification of three novel mutations and a high frequency of the Arg778Leu mutation in Korean patients with Wilson disease.
Hepatolenticular Degeneration
Isolation and characterization of a human liver cDNA as a candidate gene for Wilson disease.
Hepatolenticular Degeneration
Late neurological presentations of Wilson disease patients in French population and identification of 8 novel mutations in the ATP7B gene.
Hepatolenticular Degeneration
Molecular analysis of Wilson disease in Taiwan: identification of one novel mutation and evidence of haplotype-mutation association.
Hepatolenticular Degeneration
Monozygotic female twins discordant for phenotype of Wilson's disease.
Hepatolenticular Degeneration
Mutation analysis and characterization of alternative splice variants of the Wilson disease gene ATP7B.
Hepatolenticular Degeneration
Mutation analysis and the correlation between genotype and phenotype of Arg778Leu mutation in chinese patients with Wilson disease.
Hepatolenticular Degeneration
Mutational analysis of ATP7B and genotype-phenotype correlation in Japanese with Wilson's disease.
Hepatolenticular Degeneration
Mutational analysis of ATP7B in Chinese Wilson disease patients.
Hepatolenticular Degeneration
NMR Characterization of Copper-Binding Domains 4-6 of ATP7B .
Hepatolenticular Degeneration
Oxidative-phosphorylation defects in liver of patients with Wilson's disease.
Hepatolenticular Degeneration
P-type ATPase from the cyanobacterium Synechococcus 7942 related to the human Menkes and Wilson disease gene products.
Hepatolenticular Degeneration
Role of the copper-binding domain in the copper transport function of ATP7B, the P-type ATPase defective in Wilson disease.
Hepatolenticular Degeneration
Sequence, mapping and disruption of CCC2, a gene that cross-complements the Ca(2+)-sensitive phenotype of csg1 mutants and encodes a P-type ATPase belonging to the Cu(2+)-ATPase subfamily.
Hepatolenticular Degeneration
Wilson disease and Menkes disease: new handles on heavy-metal transport.
Hepatolenticular Degeneration
Wilson disease: identification of two novel mutations and clinical correlation in Eastern Chinese patients.
Hepatolenticular Degeneration
Wilson disease: novel mutations in the ATP7B gene and clinical correlation in Brazilian patients.
Hepatolenticular Degeneration
[Haplotype analysis and possible founder effect at the R778L mutation of the ATP7B gene in Korean patients with Wilson's disease.]
Herpes Simplex
Solubilization of adenosine triphosphatase associated with herpes simplex virus.
Herpes Simplex
Some properties of the adenosine triphosphatase associated with herpes simplex virus and nuclear membrane of host cells.
Herpes Simplex
The herpes simplex virus type 1 origin-binding protein. sequence-specific activation of adenosine triphosphatase activity by a double-stranded DNA containing box I.
Herpes Zoster
Mesothelial cells: a cellular surrogate for tissue engineering of corneal endothelium.
Herpes Zoster
Ouabain chronic infusion enhances the growth and steroidogenic capacity of rat adrenal zona glomerulosa: the possible involvement of the endothelin system.
Histiocytosis, Langerhans-Cell
Histiocytosis X cells and Langerhans cells: enzyme histochemical and immunologic similarities.
Homocystinuria
In vitro homocysteine inhibits platelet Na+,K+-ATPase and serum butyrylcholinesterase activities of young rats.
Homocystinuria
In vivo and in vitro effects of homocysteine on Na+, K+-ATPase activity in parietal, prefrontal and cingulate cortex of young rats.
Huntington Disease
Increased sodium plus potassium adenosine triphosphatase activity in erythrocyte membranes in Huntington's disease.
Huntington Disease
Specificity of biophysical and biochemical alterations in erythrocyte membranes in neurological disorders--Huntington's disease, Friedreich's ataxia, Alzheimer's disease, amyotrophic lateral sclerosis, and myotonic and duchenne muscular dystrophy.
Hydrops Fetalis
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.
Hydrops Fetalis
Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations.
Hyperaldosteronism
Does a digoxin-like substance participate in vascular and pressure control during dietary sodium changes in patients with primary aldosteronism?
Hyperaldosteronism
Intracellular sodium and potassium concentrations in erythrocytes of patients with primary aldosteronism.
Hyperaldosteronism
Sodium transport parameters in erythrocytes of patients with primary aldosteronism.
Hypercholesterolemia
Influence of sterols and phospholipids on sarcolemmal and sarcoplasmic reticular cation transporters.
Hyperemia
Na+/K+-ATPase plays a major role in mediating cutaneous thermal hyperemia achieved by local skin heating to 39 ºC.
Hyperemia
Reactive Hyperemia Occurs Via Activation of Inwardly Rectifying Potassium Channels and Na+/K+-ATPase in Humans.
Hyperhomocysteinemia
Concurrent folate treatment prevents Na+,K+-ATPase activity inhibition and memory impairments caused by chronic hyperhomocysteinemia during rat development.
Hyperinsulinism
Association of sick sinus syndrome with hyperinsulinemia and insulin resistance in patients with non-insulin-dependent diabetes mellitus: report of four cases.
Hyperkalemia
Altered fluid, electrolyte and mineral status in tropical disease, with an emphasis on malaria and leptospirosis.
Hyperkalemia
Digoxin-like immunoreactive substance in nonoliguric hyperkalemia of the premature infant.
Hyperkalemia
Reduction of erythrocyte (Na(+)-K+) ATPase activities in non-insulin-dependent diabetic patients with hyperkalemia.
Hyperkalemia
The role of a humoral Na+,K+-ATPase inhibitor in regulating precapillary vessel tone.
Hyperprolactinemia
Role of Na+/K(+)-ATPase in Natriuretic Effect of Prolactin in a Model of Cholestasis of Pregnancy.
Hypersensitivity
A circulating inhibitor of the platelet Na+,K+ adenosine triphosphatase (ATPase) enzyme in allergy.
Hypersensitivity
Antiarrhythmic drug amiodarone displays antifungal activity, induces irregular calcium response and intracellular acidification of Aspergillus niger - Amiodarone targets calcium and pH homeostasis of A. niger.
Hypersensitivity
Familial hemiplegic migraine type 2 does not share hypersensitivity to nitric oxide with common types of migraine.
Hypersensitivity
The relationship between airway hyperreactivity (AHR) and sodium, potassium adenosine triphosphatase (Na+,K+ ATPase) enzyme inhibition.
Hypersensitivity
[Activity of acid and alkaline phosphatases and adenosine triphosphatase in secondary allergy before and after treatment with hydrocortisone]
Hypertension
Abnormalities in the sodium transport as the causative factor for enhanced norepinephrine overflow in the spontaneously hypertensive rat.
Hypertension
Abnormalities of sodium pump function in hypertension and the role of endogenous cardiotonic steroids.
Hypertension
Acute Na+,K+-ATPase inhibition with bufalin impairs pressure natriuresis in the rat.
Hypertension
Alterations in phenylephrine-induced contractions and the vascular expression of Na+,K+-ATPase in ouabain-induced hypertension.
Hypertension
Altered erythrocyte cation transport related to hypertension or oral contraception.
Hypertension
Altered sodium pump alpha and gamma subunit gene expression in nephron segments from hypertensive rats.
Hypertension
Altered subcellular distribution of Na+,K+-ATPase in proximal tubules in young spontaneously hypertensive rats.
Hypertension
Brain Na+,K+-ATPase isozyme activity and protein expression in ouabain-induced hypertension.
Hypertension
Cardenolide and bufadienolide ligands of the sodium pump. How they work together in NaCl sensitive hypertension.
Hypertension
Characterization of a Na+/K+-ATPase inhibitor from human plasma: preliminary data.
Hypertension
Cicletanine reverses vasoconstriction induced by the endogenous sodium pump ligand, marinobufagenin, via a protein kinase C dependent mechanism.
Hypertension
Circulating bufodienolide and cardenolide sodium pump inhibitors in preeclampsia.
Hypertension
Commentary. The sodium pump in cardiovascular muscle in hypertension: whose hypothesis?
Hypertension
Demonstration of a ouabainlike plasma compound in hypertension prone and hypertension resistant rats.
Hypertension
Dietary salt, intracellular ion homeostasis and hypertension secondary to early-stage kidney disease.
Hypertension
Dietary Sodium Restriction and Association with Urinary Marinobufagenin, Blood Pressure, and Aortic Stiffness.
Hypertension
Differential regulation of the sodium pump alpha-subunit isoform gene by ouabain and digoxin in tissues of rats.
Hypertension
Digitalis-like factor response to hyperinsulinemia accompanying a euglycemic hyperinsulinemic clamp or oral glucose tolerance test.
Hypertension
Digitalis-like factor response to hyperinsulinemia in human pregnancy, a model of insulin resistance.
Hypertension
Does a digoxin-like substance participate in vascular and pressure control during dietary sodium changes in patients with primary aldosteronism?
Hypertension
Downstream shift in sodium pump activity along the nephron during acute hypertension.
Hypertension
Dual effect of polyphenolic compounds on cardiac Na+/K+-ATPase during development and persistence of hypertension in rats.
Hypertension
Effect of ageing and hypertension on endothelial modulation of ouabain-induced contraction and sodium pump activity in the rat aorta.
Hypertension
Effect of dietary sodium on the Na-K ATPase inhibitor in patients with essential hypertension.
Hypertension
Effect of local infusion of ouabain on human forearm vascular resistance and on response to potassium, verapamil and sodium nitroprusside.
Hypertension
Effect of maturation on renal Na+/K+-atpase and its susceptibility to nitric oxide-deficient hypertension in rats.
Hypertension
Effect of mechanical strain on expression of Na+,K+-ATPase alpha subunits in rat aortic smooth muscle cells.
Hypertension
Effects of changes in sodium balance on leucocyte sodium transport: qualitative differences in normotensive offspring of hypertensives and matched controls.
Hypertension
Effects of lead and natriuretic hormone on kinetics of sodium-potassium-activated adenosine triphosphatase: possible relevance to hypertension.
Hypertension
Effects of ouabain on adrenergic neurotransmission in spontaneously hypertensive rats.
Hypertension
Endogenous cardiac glycosides: hormones using the sodium pump as signal transducer.
Hypertension
Endogenous cardiotonic steroids and differential patterns of sodium pump inhibition in NaCl-loaded salt-sensitive and normotensive rats.
Hypertension
Endogenous ligand of alpha(1) sodium pump, marinobufagenin, is a novel mediator of sodium chloride--dependent hypertension.
Hypertension
Endogenous sodium pump inhibition: current status and therapeutic opportunities.
Hypertension
Epidemiological evidence associating dietary calcium and calcium metabolism with blood pressure.
Hypertension
Evidence for a circulating endogenous Na+-K+ pump inhibitor in low-renin hypertension.
Hypertension
Expression of sodium pump isoforms and other sodium or calcium ion transporters in the heart of hypertensive patients.
Hypertension
Facilitatory effects of ouabain and digitalis-like substance on adrenergic transmission in hypertension.
Hypertension
Function of the sodium pump in arterial smooth muscle in experimental hypertension: role of pressure.
Hypertension
Functional differences in blood vessels determined from studies with calcium-channel blockers. Functional changes in forearm resistance vessels of men with primary hypertension.
Hypertension
Further biochemical characterization of an Na+ pump inhibitor purified from human urine.
Hypertension
Genetic and genomic evidence for an important role of the Na+/H+ exchanger 3 in blood pressure regulation and angiotensin II-induced hypertension.
Hypertension
Genetic determinants of emotionality and stress response in AcB/BcA recombinant congenic mice and in silico evidence of convergence with cardiovascular candidate genes.
Hypertension
Humoral sodium transport inhibitor in acute volume expansion and low renin hypertension.
Hypertension
Hypertension and inhibition of the sodium pump: a strong link but in which chain?
Hypertension
Hypertension-linked mutation in the adducin alpha-subunit leads to higher AP2-mu2 phosphorylation and impaired Na+,K+-ATPase trafficking in response to GPCR signals and intracellular sodium.
Hypertension
Hypothetical mechanism of sodium pump regulation by estradiol under primary hypertension.
Hypertension
In ability of Na+,K+-ATPase inhibitor to cause hypertension in sodium-loaded or deoxycorticosterone-treated one kidney rats.
Hypertension
Increased activity of digoxin-like substance in low-renin hypertension in acromegaly.
Hypertension
Inhibitors of Na-K-ATPase in human urine: effects of ouabain-like factors and of vanadium-diascorbate on calcium mobilization in rat vascular smooth muscle cells: comparison with the effects of ouabain, angiotensin II, and arginine-vasopressin.
Hypertension
Intracellular sodium and potassium concentrations in erythrocytes of patients with primary aldosteronism.
Hypertension
Isolation and characterization of a specific endogenous Na+,K+-ATPase inhibitor from bovine adrenal.
Hypertension
Lack of effect of acute alcohol ingestion on erythrocyte Na+, K+ -ATPase activity or passive sodium uptake in vivo in man.
Hypertension
Lenticular rubidium uptake and plasma renin activity in weanling cataract-prone salt-sensitive rats.
Hypertension
Leucocyte electrolytes and sodium efflux rate constants in the hypertension of pre-eclampsia.
Hypertension
Leucocyte membrane sodium transport in normotensive populations: dissociation of abnormalities of sodium efflux from raised blood-pressure.
Hypertension
Leucocyte sodium content and sodium pump activity in overweight and lean hypertensives.
Hypertension
Low-concentration ouabain does not inhibit noradrenaline-induced contraction of human resistance arteries.
Hypertension
Magnesium supplementation prevents the development of alcohol-induced hypertension.
Hypertension
Main results of the ouabain and adducin for Specific Intervention on Sodium in Hypertension Trial (OASIS-HT): a randomized placebo-controlled phase-2 dose-finding study of rostafuroxin.
Hypertension
Marinobufagenin may mediate the impact of salty diets on left ventricular hypertrophy by disrupting the protective function of coronary microvascular endothelium.
Hypertension
Measurement by bioluminescence technique of erythrocyte membrane Na+,K+-ATPase activity in hypertensive patients.
Hypertension
Mechanism of garlic (Allium sativum) induced reduction of hypertension in 2K-1C rats: a possible mediation of Na/H exchanger isoform-1.
Hypertension
Na+,K+-ATPase activity and responsiveness of vascular smooth muscle to norepinephrine, angiotensin II and calcium ionophore A23187 in guinea pig aortic strips.
Hypertension
Na+/K+-ATPase alpha isoforms expression in stroke-prone spontaneously hypertensive rat heart ventricles: effect of salt loading and lacidipine treatment.
Hypertension
Observations on the "cascade" of Na-K-ATPase inhibitory and digoxin-like immunoreactive material in human urine: possible relevance to essential hypertension.
Hypertension
Oleic and linoleic acids are active principles in Nigella sativa and stabilize an E(2)P conformation of the Na,K-ATPase. Fatty acids differentially regulate cardiac glycoside interaction with the pump.
Hypertension
Ouabain stimulates endothelin release and expression in human endothelial cells without inhibiting the sodium pump.
Hypertension
Ouabain vasoconstricts human forearm arterioles through alpha-adrenergic stimulation.
Hypertension
Ouabainlike Na+,K+-ATPase inhibitor in the plasma of normotensive and hypertensive humans and rats.
Hypertension
Pharmacologic agents for the in vivo detection of vascular sodium transport defects in hypertension.
Hypertension
Plasma Na+-K+ ATPase inhibitory activity in normal and hypertensive subjects: relationship to intracellular electrolytes and blood pressure.
Hypertension
Plasma sodium pump inhibitor in essential hypertension and normotensive subjects with hypertensive heredity.
Hypertension
Platelet sodium kinetics, blood pressure and serum urate: aberrations in non-obese men at risk for type 2 diabetes mellitus.
Hypertension
Polymorphisms in migraine-associated gene, atp1a2, and ischemic stroke risk in a biracial population: the genetics of early onset stroke study.
Hypertension
Potassium in skeletal muscle in untreated primary hypertension and in chronic renal failure, studied by X-ray fluorescence technique.
Hypertension
PP089. Analytical aspects of marinobufagenin and its applications in the diagnosis of preeclampsia.
Hypertension
Problems and pitfalls in the isolation of an endogenous Na+, K+-ATPase inhibitor.
Hypertension
Proximal tubule Na transporter responses are the same during acute and chronic hypertension.
Hypertension
Pulmonary arterial hypertension in familial hemiplegic migraine with ATP1A2 channelopathy.
Hypertension
Race, sex, and family history of hypertension and erythrocyte sodium pump [3H]ouabain binding.
Hypertension
Raised sodium pump activity and a circulating sodium transport inhibitor demonstrated on red blood cells of patients with untreated essential hypertension: correlation of pump activity with potassium permeability.
Hypertension
Regulation of blood pressure during long-term ouabain infusion in Long-Evans rats.
Hypertension
Regulation of Na+,K+-ATPase alpha-subunit expression by mechanical strain in aortic smooth muscle cells.
Hypertension
Regulation of Na+/K+-ATPase by Estradiol and IGF-1 in Cardio-Metabolic Diseases.
Hypertension
Regulation of sodium/potassium ATPase activity: impact on salt balance and vascular contractility.
Hypertension
Relationship of Na-K-ATPase inhibitors to blood-pressure regulation in continuous ambulatory peritoneal dialysis and hemodialysis.
Hypertension
Renal sodium pump regulation in deoxycorticosterone salt hypertension in the rat.
Hypertension
Revealing of endogenous Marinobufagin by an ultra-specific and sensitive UHPLC-MS/MS assay in pregnant women.
Hypertension
Reversal of sodium pump inhibitor induced vascular smooth muscle contraction with digibind. Stoichiometry and its implications.
Hypertension
Reversible inhibition of leucocyte sodium pumps by a circulating serum factor in essential hypertension.
Hypertension
Role of ouabain-like factors and Na-K-ATPase inhibitors in hypertension--some old and recent findings.
Hypertension
Salt and gene expression: evidence for [Na(+)] i/[K (+)] i-mediated signaling pathways.
Hypertension
Salt sensitivity in normotensives with family history of hypertension: studies of membrane transport, intracellular electrolytes and alpha 2-adrenergic receptors.
Hypertension
Sodium pump activity and norepinephrine responsiveness of femoral arterial smooth muscle from DOCA-salt rats.
Hypertension
Sodium pump and Na+/H+ activities in uremic erythrocytes. A microcalorimetric and pH-metric study.
Hypertension
Sodium pump inhibition and regional expression of sodium pump alpha-isoforms in lens.
Hypertension
Sodium transport in erythrocytes: differences between normal children and children with primary and secondary hypertension.
Hypertension
Sodium-potassium-adenosine triphosphatase in nephron segments of spontaneously hypertensive rats.
Hypertension
Species sensitivity of the sodium pump to a circulating ouabain-like inhibitor in acute hypervolemia and DOCA hypertension: comparison with ouabain.
Hypertension
Structure-activity relationships for the hypertensinogenic activity of ouabain: role of the sugar and lactone ring.
Hypertension
Studies on the role of sodium- and potassium-activated adenosine triphosphatase inhibition in the pathogenesis of human hypertension. Changes in vascular and cardiac function following inhibition of the sodium pump in normotensive subjects and effects of calcium entry blockade.
Hypertension
Sustained volume expansion and [Na,K]ATPase inhibition in chronic renal failure.
Hypertension
Sympathetic vasoconstriction as a mechanism of action of ouabain in forearm arterioles of hypertensive patients.
Hypertension
The dilator response to K+ is reduced in the forearm resistance vessels of men with primary hypertension.
Hypertension
The role of a humoral Na+,K+-ATPase inhibitor in regulating precapillary vessel tone.
Hypertension
The role of a humoral sodium-potassium pump inhibitor in low-renin hypertension.
Hypertension
The role of endogenous inhibition of Na-K-ATPase in human hypertension--sodium pump activity as a determinant of peripheral vascular resistance.
Hypertension
The role of sodium-potassium adenosine triphosphatase in the regulation of membrane fluidity of erythrocytes in spontaneously hypertensive rats: an electron paramagnetic resonance investigation.
Hypertension
The role of vascular Na,K-ATPase activity in salt induced hypertension in Dahl rats.
Hypertension
The sodium pump and hypertension: a physiological role for the cardiac glycoside binding site of the Na,K-ATPase.
Hypertension
Three red cell sodium transport systems in hypertensive and normotensive Utah adults.
Hypertension
Transactivation of epidermal growth factor receptor in vascular and renal systems in rats with experimental hyperleptinemia: role in leptin-induced hypertension.
Hypertension
Transgenic overexpression of translationally controlled tumor protein induces systemic hypertension via repression of Na+,K+-ATPase.
Hypertension
Two-dimensional, sex-specific autosomal linkage scan of the number of sodium pump sites.
Hypertension
Vascular endothelium as a target for endogenous ouabain: studies on the effect of ouabain on human endothelial cells.
Hypertension
Vascular smooth muscle membrane potentials in rats with one-kidney, one clip and reduced renal mass-saline hypertension: the influence of a humoral sodium pump inhibitor.
Hypertension
Vascular sodium pump activity kinetics in early and advanced stages of deoxycorticosterone-salt hypertension in rats.
Hypertension
Wistar rats resistant to the hypertensive effects of ouabain exhibit enhanced cardiac vagal activity and elevated plasma levels of calcitonin gene-related peptide.
Hypertension
[(Na + --K + )-dependent adenosine triphosphatase in the renal medulla and cortex of rabbits with ischemic cerebral hypertension]
Hypertension
[Changes in the glycolytic pathway in patients with essential arterial hypertension]
Hypertension
[Effect of ouabain on intracellular Ca(2+) concentration in rat vascular smooth muscle cells in vitro].
Hypertension
[Hereditary salt sensitivity as a cause of essential hypertension: studies of membrane transport and intracellular electrolytes]
Hypertension
[Is there a relation between the presence in the serum of patients with arterial hypertension of a protein component with molecular weight of 15 kD and the inhibitory effect of the serum on Na,K-ATPase?]
Hypertension
[Physiologic role of the sodium pump. Implications for the study of arterial hypertension]
Hypertension
[Preparation and characterization of polyclonal antibodies against rat sodium pump alpha 2 subunit M1-M2 extra membrane fragment].
Hypertension, Pregnancy-Induced
Modifications induced by plasma of gestational hypertensive women on the Na+/K+-ATPase obtained from human placenta.
Hypertension, Pregnancy-Induced
Platelet sodium pump and sodium potassium cotransport activity in nonpregnant, normotensive, and hypertensive pregnant women.
Hypertension, Pregnancy-Induced
Pregnancy induced hypertension and sodium pump function in erythrocytes.
Hypertension, Pregnancy-Induced
Sodium pump numbers and cation transport of lymphocytes in pregnancy-induced hypertension.
Hypertension, Pregnancy-Induced
[Ganoderma spores may regulate the levels of mitochondria-related molecular substances in hippocampus of young rats birthed by rats with gestational hypertension]
Hypertension, Renal
Dietary salt, intracellular ion homeostasis and hypertension secondary to early-stage kidney disease.
Hypertension, Renovascular
Measurement by bioluminescence technique of erythrocyte membrane Na+,K+-ATPase activity in hypertensive patients.
Hypertension, Renovascular
Sodium pump activity in arteries of rats with Goldblatt hypertension.
Hypertension, Renovascular
Sodium pump activity in thymocytes of rats with Goldblatt hypertension.
Hyperthyroidism
Abnormalities in the sodium pump of erythrocytes from patients with hyperthyroidism.
Hyperthyroidism
Catecholamine and thyroid hormone influence on brown fat Na+, K+-ATPase activity and thermogenesis in the rat.
Hyperthyroidism
Changes in acetylcholinesterase, Na+,K+-ATPase, and Mg2+-ATPase activities in the frontal cortex and the hippocampus of hyper- and hypothyroid adult rats.
Hyperthyroidism
Effect of thyroid status on the development of the different molecular forms of Na+,K+-ATPase in rat brain.
Hyperthyroidism
Effects of oxidative stress on the erythrocyte Na+,K+ ATPase activity in female hyperthyroid patients.
Hyperthyroidism
Effects of thyroid hormone on sodium pump sites, sodium content, and contractile responses to cardiac glycosides in cultured chick ventricular cells.
Hyperthyroidism
Erythrocyte sodium fluxes, ouabain binding sites, and Na+,K(+)-ATPase activity in hyperthyroidism.
Hyperthyroidism
Induction of the ATP-dependent proteolytic system in guinea pig reticulocyte lysates by triiodothyronine.
Hyperthyroidism
Ion flux and Na+,K+-ATPase activity of erythrocytes and leucocytes in thyroid disease.
Hyperthyroidism
Na+K+ATPase activity and ouabain binding sites in erythrocytes in hyperthyroidism before and after treatment.
Hyperthyroidism
No major thermogenic role for (Na+ + K+)-dependent adenosine triphosphatase apparent in hepatocytes from hyperthyroid rats.
Hyperthyroidism
Ouabain-binding sites of reticulocytes from guinea pigs treated with triiodothyronine.
Hyperthyroidism
Stimulation of the Na+,K(+)-ATPase activity of K562 human erythroleukemia cells by triiodothyronine.
Hyperthyroidism
The contribution of ATP turnover by the Na+/K+-ATPase to the rate of respiration of hepatocytes. Effects of thyroid status and fatty acids.
Hyperthyroidism
The effect of hyperthyroidism on in vivo aging of erythrocyte ouabain-binding sites and intracellular sodium and potassium.
Hyperthyroidism
[A histochemical study of gastric adenosine triphosphatase, alkaline and acid phosphatase in experimental hypo- and hyperthyroidism]
Hyperthyroidism
[Adenosine triphosphatase activity of the liver and micro- and macroelement levels in the organism of white rats in experimental hyperthyroidism]
Hyperthyroidism
[THE ADENOSINE TRIPHOSPHATASE ACTIVITY OF LEUKOCYTE HOMOGENATES IN HYPERTHYROIDISM.]
Hypoglycemia
The role of spreading depression, spreading depolarization and spreading ischemia in neurological disease.
Hypokalemia
Effects of hypokalemia on the cardiotropic actions of digoxin in dogs. Correlation with inhibition of cardiac Na+,K+-adenosine triphosphatase.
Hypokalemia
Expression of Na(+)-K(+)-ATPase alpha- and beta-subunits along rat nephron: isoform specificity and response to hypokalemia.
Hypokalemia
The role of a humoral Na+,K+-ATPase inhibitor in regulating precapillary vessel tone.
Hypoparathyroidism
X-linked hypoparathyroidism region on Xq27 is evolutionarily conserved with regions on 3q26 and 13q34 and contains a novel P-type ATPase.
Hypotension
Modulation of Cardiovascular Function in Primary Hypertension in Rat by SKA-31, an Activator of KCa2.x and KCa3.1 Channels.
Hypothyroidism
Effect of thyroid status on the development of the different molecular forms of Na+,K+-ATPase in rat brain.
Hypothyroidism
Ion flux and Na+,K+-ATPase activity of erythrocytes and leucocytes in thyroid disease.
Hypothyroidism
Modulation of glutamate levels and Na+,K+-ATPase activity contributes to the chrysin memory recovery in hypothyroidism mice.
Hypothyroidism
The Effects of Altered Membrane Cholesterol Levels on Sodium Pump Activity in Subclinical Hypothyroidism.
Infections
Adenosine triphosphatase activity associated with bovine erythrocyte membranes during infection with Anaplasma marginale.
Infections
Altered expression of sodium pump isoforms in the inflamed intestine of Trichinella spiralis-infected rats.
Infections
Changes in Na,K-ATPase, sodium ion, and glucose transport in isolated enterocytes in an experimental model of malabsorption.
Infections
Effects of Cryptocaryon irritans infection on the survival, feeding, respiratory rate and ionic regulation of the marbled rockfish Sebastiscus marmoratus.
Infections
Effects of glycyrrhizin on the growth cycle and ATPase activity of PRRSV-2-infected MARC-145 cells.
Infections
Hypotheses about sub-optimal hydration in the weeks before coronavirus disease (COVID-19) as a risk factor for dying from COVID-19.
Infections
Induction of a Na+/K+-ATPase-dependent form of autophagy triggers preferential cell death of human immunodeficiency virus type-1-infected macrophages.
Infections
Multiplex PCR for the diagnosis of red sea bream iridoviruses isolated in Korea.
Infections
PDE1 encodes a P-type ATPase involved in appressorium-mediated plant infection by the rice blast fungus Magnaporthe grisea.
Infections
Schistosoma mansoni: fine structural localization of tegumental adenosine triphosphatases.
Infections
Screening of Natural Extracts for Inhibitors against Japanese Encephalitis Virus Infection.
Infections
Selective cell death of latently HIV-infected CD4+ T cells mediated by autosis inducing nanopeptides.
Infections
The antidiarrhoeal evaluation of Psidium guajava L. against enteropathogenic Escherichia coli induced infectious diarrhoea.
Infections
The Vacuolar Ca2+ ATPase Pump Pmc1p Is Required for Candida albicans Pathogenesis.
Infections
Thyroid status and adenosine triphosphatase activity in experimental Trypanosoma congolense infection in rabbits.
Influenza, Human
Glycolytic control of vacuolar-type ATPase activity: A mechanism to regulate influenza viral infection.
Influenza, Human
Na+/K+-ATPase as a Target of Cardiac Glycosides for the Treatment of SARS-CoV-2 Infection.
Insulin Resistance
Altered expression and insulin-induced trafficking of Na+, K+-ATPase in rat skeletal muscle: effects of high fat diet and exercise.
Insulin Resistance
Association of sick sinus syndrome with hyperinsulinemia and insulin resistance in patients with non-insulin-dependent diabetes mellitus: report of four cases.
Insulin Resistance
DR-region of Na+/K+-ATPase is a target to ameliorate hepatic insulin resistance in obese diabetic mice.
Insulin Resistance
Expression and Cellular Distribution of Glucose Transporters and Alpha Subunits of Na+/K+-ATPase in the Heart of Fructose-fed Female Rats: The Role of Estradiol.
Insulin Resistance
Short-term K(+) deprivation provokes insulin resistance of cellular K(+) uptake revealed with the K(+) clamp.
Insulin Resistance
The effect of oral glucose on the leucocyte sodium pump in normal and obese subjects.
Intellectual Disability
Asparagine-905 of the mammalian phospholipid flippase ATP8A2 is essential for lipid substrate-induced activation of ATP8A2 dephosphorylation.
Intellectual Disability
Early Treatment in Acute Severe Encephalopathy Caused by ATP1A2 Mutation of Familial Hemiplegic Migraine Type 2: Case Report and Literature Review.
Intellectual Disability
Functional correlation of ATP1A2 mutations with phenotypic spectrum: from pure hemiplegic migraine to its variant forms.
Intellectual Disability
Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation.
Intermittent Claudication
Histochemical changes in striated muscle in patients with intermittent claudication.
Intestinal Volvulus
Ivermectin: concentration-dependent effects on adenosine triphosphatases in adult worms of Onchocerca volvulus.
Intraabdominal Infections
Increased hepatic microsomal adenosine triphosphatase activity secondary to intra-abdominal infection.
Intracranial Embolism
Microsphere embolism-induced changes in noradrenaline uptake of the cerebral cortex in rats.
Iron Deficiencies
Changes in the cochlear iron enzymes and adenosine triphosphatase in experimental iron deficiency.
Ischemic Stroke
Magnesium lithospermate B possesses inhibitory activity on Na+,K+-ATPase and neuroprotective effects against ischemic stroke.
Ischemic Stroke
Polymorphisms in migraine-associated gene, atp1a2, and ischemic stroke risk in a biracial population: the genetics of early onset stroke study.
Kidney Diseases
Maximum binding of ouabain to erythrocytes in relation to a family history of essential hypertension, sodium balance and body weight in normotensive children.
Kidney Failure, Chronic
Abnormal cation transport in uremia. Mechanisms in adipocytes and skeletal muscle from uremic rats.
Kidney Failure, Chronic
Biochemical abnormalities of platelets in renal failure. Evidence for decreased platelet serotonin, adenosine diphosphate and Mg-dependent adenosine triphosphatase.
Kidney Failure, Chronic
Effects of acute and chronic uremia on active cation transport in rat myocardium.
Kidney Failure, Chronic
Garlic (Allium sativum) exhibits a cardioprotective effect in experimental chronic renal failure rat model by reducing oxidative stress and controlling cardiac Na+/K+-ATPase activity and Ca2+ levels.
Kidney Failure, Chronic
Inhibition of Na+,K+-stimulated ATPase in the cochlea of the guinea pig. A potential cause of disturbed inner ear function in terminal renal failure.
Kidney Failure, Chronic
Marinobufagenin impairs first trimester cytotrophoblast differentiation.
Kidney Failure, Chronic
Potassium in skeletal muscle in untreated primary hypertension and in chronic renal failure, studied by X-ray fluorescence technique.
Kidney Failure, Chronic
Red blood cell calcium level in chronic renal failure: effect of continuous ambulatory peritoneal dialysis.
Kidney Failure, Chronic
Reversal of sodium pump inhibitor induced vascular smooth muscle contraction with digibind. Stoichiometry and its implications.
Kidney Failure, Chronic
Specificity of the volume-sensitive sodium pump inhibitor isolated from human peritoneal dialysate in chronic renal failure.
Kidney Failure, Chronic
[Effect of hemodialysis on the erythrocyte sodium, potassium adenosine triphosphatase activity in children with chronic renal failure]
Kidney Neoplasms
Cardiotonic Steroids-Mediated Targeting of the Na(+)/K(+)-ATPase to Combat Chemoresistant Cancers.
Kwashiorkor
Erythrocyte membrane Na+ and K+ activated adenosine triphosphatase in protein-calorie malnutrition.
Lecithin Cholesterol Acyltransferase Deficiency
Study of erythrocytes in a hereditary hemolytic syndrome (HHS): comparison with erythrocytes in lecithin:cholesterol acyltransferase (LCAT) deficiency.
Leigh Disease
A novel mitochondrial ATPase 6 point mutation in familial bilateral striatal necrosis.
Lesch-Nyhan Syndrome
Effect of hypoxanthine on Na+,K+-ATPase activity and some parameters of oxidative stress in rat striatum.
Leukemia
Electron microscopic observations on the adenosine triphosphatase activity of a murine (Rauscher) and a canine leukemia virus.
Leukemia
Expression of multiple Na+,K+-adenosine triphosphatase isoform genes in human hematopoietic cells. Behavior of the novel A3 isoform during induced maturation of HL60 cells.
Leukemia
Membrane transport changes in an adriamycin-resistant murine leukemia cell line and in its sensitive parental cell line.
Leukemia
[Demonstration of adenosine triphosphatase in blood smears of acute leukemias and comparison with other enzyme-cytochemical reactions]
Leukemia
[Stereological characteristics and enzymatic activity of myocardial capillaries in different variants of pathology and death (data from immediate autopsies)]
Leukemia, Erythroblastic, Acute
Characterization of a Ca2+-stimulated Mg2+-dependent adenosine triphosphatase in Friend murine erythroleukemia cell plasma membranes.
Leukemia, Erythroblastic, Acute
The program of Friend cell erythroid differentiation: early changes in Na+/K+ ATPase function.
Leukemia, Megakaryoblastic, Acute
[Effects of ouabain at low concentrations on growth of leukemia cells]
Leukemia, Myeloid, Acute
Targeting acute myeloid leukemia dependency on VCP-mediated DNA repair through a selective second-generation small-molecule inhibitor.
Lichen Planus, Oral
Assessment of langerhans cells in oral lichen planus by ATPase histochemistry: a clinicopathologic correlation.
Liver Diseases
Assessment of Adenosine Triphosphatase Phospholipid Transporting 8B1 (ATP8B1) Function in Patients With Cholestasis With ATP8B1 Deficiency by Using Peripheral Blood Monocyte-Derived Macrophages.
Liver Diseases
Evidence that adenosine triphosphatase is one of the mitochondrial antigens of autoimmune liver disease [proceedings]
Liver Diseases
FIC1, a P-type ATPase linked to cholestatic liver disease, has homologues (ATP8B2 and ATP8B3) expressed throughout the body.
Liver Diseases
Inhibition of rat brain Na+,K+-ATPase activity by serum from patients with fulminant hepatic failure.
Liver Diseases
[Adenosine triphosphatase activity of erythrocytes in liver diseases in children]
Liver Diseases
[Comparative characteristics of adenosine triphosphatase activity in the erythrocytes of patients with acute and chronic liver diseases, chronic cholecystitis and in HBs antigen carriers]
Liver Failure, Acute
Inhibition of rat brain Na+,K+-ATPase activity by serum from patients with fulminant hepatic failure.
Liver Neoplasms
Oxidative Stress and Apoptotic Responses Elicited by Nostoc-Synthesized Silver Nanoparticles against Different Cancer Cell Lines.
Liver Neoplasms, Experimental
Membranous effects on adenosine triphosphatase activities of mitochondria from rat liver and Morris hepatoma 3924A.
Lung Injury
Electroporation-mediated in vivo gene delivery of the Na+/K+-ATPase pump reduced lung injury in a mouse model of lung contusion.
Lung Injury
Improving survival by increasing lung edema clearance: is airspace delivery of dopamine a solution?
Lung Injury
Omega-9 Oleic Acid Induces Fatty Acid Oxidation and Decreases Organ Dysfunction and Mortality in Experimental Sepsis.
Lung Neoplasms
Cardiotonic Steroids-Mediated Na+/K+-ATPase Targeting Could Circumvent Various Chemoresistance Pathways.
Lung Neoplasms
Clinical outcome of cisplatin-based chemotherapy is associated with the polymorphisms of GSTP1 and XRCC1 in advanced non-small cell lung cancer patients.
Lung Neoplasms
Copper-transporting P-type adenosine triphosphatase (ATP7A) is associated with platinum-resistance in non-small cell lung cancer (NSCLC).
Lung Neoplasms
Cytotoxic and non-cytotoxic cardiac glycosides isolated from the combined flowers, leaves, and twigs of Streblus asper.
Lung Neoplasms
Cytotoxicity of glucoevatromonoside alone and in combination with chemotherapy drugs and their effects on Na+,K+-ATPase and ion channels on lung cancer cells.
Lung Neoplasms
Evaluation of the relationship of erythrocyte membrane Na+/K+-ATPase enzyme activity and tumor response to chemoradiotherapy in patients diagnosed with locally advanced nonsmall cell lung cancer and glioblastoma multiforme.
Lung Neoplasms
Expression of copper-transporting P-type adenosine triphosphatase (ATP7B) correlates with cisplatin resistance in human non-small cell lung cancer xenografts.
Lung Neoplasms
MiR-495 enhances the sensitivity of non-small cell lung cancer cells to platinum by modulation of copper-transporting P-type adenosine triphosphatase A (ATP7A).
Lung Neoplasms
Role of sodium pump systems to determine sensitivity to mitomycin C in non-small cell lung cancer cell lines.
Lung Neoplasms
The alpha1 subunit of the sodium pump could represent a novel target to combat non-small cell lung cancers.
Lymphoma
Malignant lymphomas in the acquired immunodeficiency syndrome. Additional evidence for a B-cell origin.
Lymphoma
Mg2+-dependent adenosine triphosphatase as an enzyme histochemical marker for the lymphomas of B-cell origin.
Lymphoma, B-Cell
Activation of novel estrogen receptor GPER results in inhibition of cardiocyte apoptosis and cardioprotection.
Lymphoma, B-Cell
Oxidative Stress and Apoptotic Responses Elicited by Nostoc-Synthesized Silver Nanoparticles against Different Cancer Cell Lines.
Lymphoma, Non-Hodgkin
An enzyme histochemical study of non-Hodgkin's lymphoma and allied disease.
Lymphoma, Non-Hodgkin
[Circadian rhythm of adenosine triphosphatase activity and 32P content in Pliss lymphosarcoma]
Malaria
PbGCbeta is essential for Plasmodium ookinete motility to invade midgut cell and for successful completion of parasite life cycle in mosquitoes.
Malnutrition
Death during recovery from severe malnutrition and its possible relationship to sodium pump activity in the leucocyte.
Malnutrition
Reduction in vitro of red cell glutathione reproduces defects of cellular sodium transport seen in oedematous malnutrition.
Malnutrition
[Subcellular distribution of the activity of the adenosine triphosphatase system during postnatal maturation of rat brain: influence of malnutrition]
Mania
Cognitive flexibility impairment and reduced frontal cortex BDNF expression in the ouabain model of mania.
Mania
Effect of ouabain on sodium pump alpha-isoform expression in an animal model of mania.
Mania
Endogenous digoxin-like immunoreactive factor (DLIF) serum concentrations are decreased in manic bipolar patients compared to normal controls.
Mania
Evaluation of neuroprotection by lithium and valproic acid against ouabain-induced cell damage.
Mania
Lithium prevents ouabain-induced behavioral changes. Toward an animal model for manic depression.
Massive Hepatic Necrosis
Preventive effect of zinc compounds, polaprezinc and zinc acetate against the onset of hepatitis in Long-Evans Cinnamon rat.
Mastocytoma
Effect of D-glucosamine on growth and several functions of cultured mastocytoma P-815 cells.
Medulloblastoma
Immunohistochemical analyses of alpha1 and alpha3 Na+/K+-ATPase subunit expression in medulloblastomas.
Melanoma
Activity of BK(Ca) channel is modulated by membrane cholesterol content and association with Na+/K+-ATPase in human melanoma IGR39 cells.
Melanoma
Cardiotonic Steroids-Mediated Na+/K+-ATPase Targeting Could Circumvent Various Chemoresistance Pathways.
Melanoma
Cardiotonic Steroids-Mediated Targeting of the Na(+)/K(+)-ATPase to Combat Chemoresistant Cancers.
Melanoma
Identification and cloning of genes displaying elevated expression as a consequence of metastatic progression in human melanoma cells by rapid subtraction hybridization.
Melanoma
The Sodium Pump alpha1 Subunit: a Disease Progression-Related Target for Metastatic Melanoma Treatment.
Memory Disorders
Modulation of glutamate levels and Na+,K+-ATPase activity contributes to the chrysin memory recovery in hypothyroidism mice.
Memory Disorders
Multitarget Effect of 2-(4-(Methylthio)phenyl)-3-(3-(piperidin-1-yl)propyl)thiazolidin-4-one in a Scopolamine-Induced Amnesic Rat Model.
Memory Disorders
The neuroprotective role of melatonin in a gestational hypermethioninemia model.
Meniere Disease
Possible functional roles of Na+,K+-ATPase in the inner ear and their relevance to Ménière's disease.
Meningitis
Increased Na+,K+-ATPase activity in the rat brain after meningitis induction by Streptococcus pneumoniae.
Menkes Kinky Hair Syndrome
13 novel putative mutations in ATP7A found in a cohort of 25 Italian families.
Menkes Kinky Hair Syndrome
Adipocyte-specific disruption of ATPase copper transporting ? in mice accelerates lipoatrophy.
Menkes Kinky Hair Syndrome
ATP7A (Menkes protein) functions in axonal targeting and synaptogenesis.
Menkes Kinky Hair Syndrome
ATP7A gene addition to the choroid plexus results in long-term rescue of the lethal copper transport defect in a Menkes disease mouse model.
Menkes Kinky Hair Syndrome
ATP7A transgenic and nontransgenic mice are resistant to high copper exposure.
Menkes Kinky Hair Syndrome
Characterization of the exon structure of the Menkes disease gene using vectorette PCR.
Menkes Kinky Hair Syndrome
Copper homeostasis in the CNS: a novel link between the NMDA receptor and copper homeostasis in the hippocampus.
Menkes Kinky Hair Syndrome
Direct interactions of adaptor protein complexes 1 and 2 with the copper transporter ATP7A mediate its anterograde and retrograde trafficking.
Menkes Kinky Hair Syndrome
Functional expression of the menkes disease protein reveals common biochemical mechanisms among the copper-transporting P-type ATPases.
Menkes Kinky Hair Syndrome
L-Threo-Dihydroxyphenylserine corrects neurochemical abnormalities in a menkes disease mouse model.
Menkes Kinky Hair Syndrome
Menkes disease diagnosed by a novel ATP7A frameshift mutation in a patient with infantile spasms-a case report.
Menkes Kinky Hair Syndrome
Molecular basis of the brindled mouse mutant (Mo(br)): a murine model of Menkes disease.
Menkes Kinky Hair Syndrome
Mutational analysis of ATP7B and genotype-phenotype correlation in Japanese with Wilson's disease.
Menkes Kinky Hair Syndrome
Safety of intracerebroventricular copper histidine in adult rats.
Menkes Kinky Hair Syndrome
Sequence, mapping and disruption of CCC2, a gene that cross-complements the Ca(2+)-sensitive phenotype of csg1 mutants and encodes a P-type ATPase belonging to the Cu(2+)-ATPase subfamily.
Menkes Kinky Hair Syndrome
Wilson disease and Menkes disease: new handles on heavy-metal transport.
Menkes Kinky Hair Syndrome
Wilson's disease: a new gene and an animal model for an old disease.
Mesothelioma
Immunohistochemical and histochemical markers of primary lung cancer, lung metastases, and pleural mesotheliomas.
Metabolic Syndrome
Decreased Na+/K+-ATPase Activity and Altered Susceptibility to Peroxidation and Lipid Composition in the Erythrocytes of Metabolic Syndrome Patients with Coronary Artery Disease.
Metabolic Syndrome
Regulation of the Na,K-ATPase: Special implications for cardiovascular complications of metabolic syndrome.
Metabolic Syndrome
Transactivation of epidermal growth factor receptor in vascular and renal systems in rats with experimental hyperleptinemia: role in leptin-induced hypertension.
Microcephaly
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.
Microcephaly
Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations.
Migraine Disorders
A case of familial hemiplegic migraine associated with a novel ATP1A2 gene mutation.
Migraine Disorders
A Chinese family with familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2.
Migraine Disorders
A genome-wide linkage scan provides evidence for both new and previously reported loci influencing common migraine.
Migraine Disorders
A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraine.
Migraine Disorders
A novel ATP1A2 gene mutation in an Irish familial hemiplegic migraine kindred.
Migraine Disorders
A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy.
Migraine Disorders
A Novel ATP1A2 Gene Variant Associated With Pure Sporadic Hemiplegic Migraine Improved After Patent Foramen Ovale Closure: A Case Report.
Migraine Disorders
A novel ATP1A2 variant associated with severe stepwise regression, hemiplegia, epilepsy and movement disorders in two unrelated patients.
Migraine Disorders
A novel de novo nonsense mutation in ATP1A2 associated with sporadic hemiplegic migraine and epileptic seizures.
Migraine Disorders
A novel lethal recognizable polymicrogyric syndrome caused by ATP1A2 homozygous truncating variants.
Migraine Disorders
A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2.
Migraine Disorders
Acute encephalopathy in familial hemiplegic migraine with ATP1A2 mutation.
Migraine Disorders
Alternating hemiplegia of childhood and a pathogenic variant of ATP1A3: a case report and pathophysiological considerations.
Migraine Disorders
Alternating hemiplegia of childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2.
Migraine Disorders
Amino acid changes in the amino terminus of the Na,K-adenosine triphosphatase alpha-2 subunit associated to familial and sporadic hemiplegic migraine.
Migraine Disorders
An Infant With Epilepsy and Recurrent Hemiplegia due to Compound Heterozygous Variants in ATP1A2.
Migraine Disorders
Analysis of amplicon-based NGS data from neurological disease gene panels: a new method for allele drop-out management.
Migraine Disorders
Analysis of chromosome 1 microsatellite markers and the FHM2-ATP1A2 gene mutations in migraine pedigrees.
Migraine Disorders
Astrocytes in Atp1a2-deficient heterozygous mice exhibit hyperactivity after induction of cortical spreading depression.
Migraine Disorders
ATP1A2 gene mutations are not present in two sisters with basilar-type migraine associated with menses.
Migraine Disorders
ATP1A2 Mutations in Migraine: Seeing through the Facets of an Ion Pump onto the Neurobiology of Disease.
Migraine Disorders
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.
Migraine Disorders
Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations.
Migraine Disorders
Biphasic neurovascular changes in prolonged migraine aura in familial hemiplegic migraine type 2.
Migraine Disorders
CACNA1A-Linked Hemiplegic Migraine in GLUT 1 Deficiency Syndrome: A Case Report.
Migraine Disorders
CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family report.
Migraine Disorders
Characteristics of cortical spreading depression and c-Fos expression in transgenic mice having a mutation associated with familial hemiplegic migraine 2.
Migraine Disorders
Clinical spectrum in three families with familial hemiplegic migraine type 2 including a novel mutation in the ATP1A2 gene.
Migraine Disorders
Coexistence of CACNA1A, ATP1A2, and KCNN3 gene mutation in migraine patients with human platelet polymorphism.
Migraine Disorders
De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report.
Migraine Disorders
De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine.
Migraine Disorders
Differential effect of FHM2 mutation on synaptic plasticity in distinct hippocampal regions.
Migraine Disorders
Diverse functional consequences of mutations in the Na+/K+-ATPase alpha2-subunit causing familial hemiplegic migraine type 2.
Migraine Disorders
Early onset severe ATP1A2 epileptic encephalopathy: Clinical characteristics and underlying mutations.
Migraine Disorders
Early Treatment in Acute Severe Encephalopathy Caused by ATP1A2 Mutation of Familial Hemiplegic Migraine Type 2: Case Report and Literature Review.
Migraine Disorders
Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations.
Migraine Disorders
Enhanced susceptibility to cortical spreading depression in two types of Na
Migraine Disorders
Epilepsy in hemiplegic migraine: Genetic mutations and clinical implications.
Migraine Disorders
Erratum to: De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report.
Migraine Disorders
Exploring Neuronal Vulnerability to Head Trauma Using a Whole Exome Approach.
Migraine Disorders
Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation.
Migraine Disorders
Familial hemiplegic migraine mutations affect Na,K-ATPase domain interactions.
Migraine Disorders
Familial hemiplegic migraine presenting as recurrent encephalopathy in a Native Indian family.
Migraine Disorders
Familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2.
Migraine Disorders
Familial Hemiplegic Migraine Type 3 (FHM3) With an SCN1A Mutation in a Chinese Family: A Case Report.
Migraine Disorders
Familial Hemiplegic Migraine with an ATP1A4 Mutation: Clinical Spectrum and Carbamazepine Efficacy.
Migraine Disorders
Familial Hemiplegic Migraine With Asymmetric Encephalopathy Secondary to ATP1A2 Mutation: A Case Series.
Migraine Disorders
Familial Hemiplegic Migraine with Severe Attacks: A New Report with ATP1A2 Mutation.
Migraine Disorders
First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine.
Migraine Disorders
Functional analysis of human Na(+)/K(+)-ATPase familial or sporadic hemiplegic migraine mutations expressed in Xenopus oocytes.
Migraine Disorders
Functional characterization of a novel C-terminal ATP1A2 mutation causing hemiplegic migraine and epilepsy.
Migraine Disorders
Functional correlation of ATP1A2 mutations with phenotypic spectrum: from pure hemiplegic migraine to its variant forms.
Migraine Disorders
Genetic effects of ATP1A2 in familial hemiplegic migraine type II and animal models.
Migraine Disorders
Genetic studies of Polish migraine patients: screening for causative mutations in four migraine-associated genes.
Migraine Disorders
Genetics of migraine: an update with special attention to genetic comorbidity.
Migraine Disorders
Genome-wide screen for modifiers of Na + /K + ATPase alleles identifies critical genetic loci.
Migraine Disorders
Genomewide significant linkage to migrainous headache on chromosome 5q21.
Migraine Disorders
Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2.
Migraine Disorders
Haplotype-based systematic association studies of ATP1A2 in migraine with aura.
Migraine Disorders
Hemiplegic migraine type 2 caused by a novel variant within the P-type ATPase motif in ATP1A2 concomitant with a CACNA1A variant.
Migraine Disorders
Hemiplegic migraine with reversible cerebral vasoconstriction caused by ATP1A2 mutations.
Migraine Disorders
Impaired plasma membrane targeting or protein stability by certain ATP1A2 mutations identified in sporadic or familial hemiplegic migraine.
Migraine Disorders
Increased susceptibility to cortical spreading depression and epileptiform activity in a mouse model for FHM2.
Migraine Disorders
Inhibition of phosphorylation of na+,k+-ATPase by mutations causing familial hemiplegic migraine.
Migraine Disorders
Insights into the Pathology of the ?2-Na(+)/K(+)-ATPase in Neurological Disorders; Lessons from Animal Models.
Migraine Disorders
Intravenous Nimodipine Treatment for Severe Episode of ATP1A2 Hemiplegic Migraine.
Migraine Disorders
Kinetic alterations due to a missense mutation in the Na,K-ATPase alpha2 subunit cause familial hemiplegic migraine type 2.
Migraine Disorders
Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families.
Migraine Disorders
Migraine and epilepsy: A focus on overlapping clinical, pathophysiological, molecular, and therapeutic aspects.
Migraine Disorders
Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4.
Migraine Disorders
Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures.
Migraine Disorders
Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.
Migraine Disorders
Na+/K+-ATPase ? isoform deficiency results in distinct spreading depolarization phenotypes.
Migraine Disorders
Neurovascular changes in prolonged migraine aura in FHM with a novel ATP1A2 gene mutation.
Migraine Disorders
New discoveries about the second gene for familial hemiplegic migraine, ATP1A2.
Migraine Disorders
No mutations in CACNA1A and ATP1A2 in probands with common types of migraine.
Migraine Disorders
Novel missense mutation in the ATP1A2 gene associated with atypical sporapedic hemiplegic migraine.
Migraine Disorders
Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions.
Migraine Disorders
Opening of the blood-brain barrier preceding cortical edema in a severe attack of FHM type II.
Migraine Disorders
Partially Reversible Cortical Metabolic Dysfunction in Familial Hemiplegic Migraine With Prolonged Aura.
Migraine Disorders
Physical mapping and characterization of the human Na,K-ATPase isoform, ATP1A4.
Migraine Disorders
Polymorphisms in migraine-associated gene, atp1a2, and ischemic stroke risk in a biracial population: the genetics of early onset stroke study.
Migraine Disorders
Prolonged Hyperperfusion in a Child With ATP1A2 Defect-Related Hemiplegic Migraine.
Migraine Disorders
Prolonged sporadic hemiplegic migraine associated with a novel de novo missense ATP1A2 gene mutation.
Migraine Disorders
Pulmonary arterial hypertension in familial hemiplegic migraine with ATP1A2 channelopathy.
Migraine Disorders
Rare missense variants in ATP1A2 in families with clustering of common forms of migraine.
Migraine Disorders
Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine.
Migraine Disorders
Recurrent coma and fever in familial hemiplegic migraine type 2. A prospective 15-year follow-up of a large family with a novel ATP1A2 mutation.
Migraine Disorders
Screen for CACNA1A and ATP1A2 mutations in sporadic hemiplegic migraine patients.
Migraine Disorders
Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies.
Migraine Disorders
Serial magnetic resonance imaging findings during severe attacks of familial hemiplegic migraine type 2: a case report.
Migraine Disorders
Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutation.
Migraine Disorders
Sodium Pumps Mediate Activity-Dependent Changes in Mammalian Motor Networks.
Migraine Disorders
Sporadic Hemiplegic Migraine with ATP1A2 and Prothrombin Gene Mutations.
Migraine Disorders
The CACNA1A and ATP1A2 genes are not involved in dominantly inherited migraine with aura.
Migraine Disorders
The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families.
Migraine Disorders
The Influence of Na(+), K(+)-ATPase on Glutamate Signaling in Neurodegenerative Diseases and Senescence.
Migraine Disorders
The kinetics of non-synaptically triggered acute excitotoxic responses in the central nervous system observed using intrinsic optical signals.
Migraine Disorders
The structure of the Na+,K+-ATPase and mapping of isoform differences and disease-related mutations.
Migraine Disorders
Toward a molecular genetic classification of familial hemiplegic migraine.
Migraine Disorders
Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine.
Migraine Disorders
Two novel functional mutations in the Na+,K+-ATPase alpha2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes.
Migraine Disorders
Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants.
Migraine Disorders
Variable manifestations of familial hemiplegic migraine associated with reversible cerebral edema in children.
Migraine Disorders
[Genetics of migraines: from ionic channels to single nucleotide polymorphisms?]
Migraine with Aura
A case of familial hemiplegic migraine associated with a novel ATP1A2 gene mutation.
Migraine with Aura
A Chinese family with familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2.
Migraine with Aura
A genome-wide linkage scan provides evidence for both new and previously reported loci influencing common migraine.
Migraine with Aura
A novel ATP1A2 gene mutation in an Irish familial hemiplegic migraine kindred.
Migraine with Aura
A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy.
Migraine with Aura
A novel ATP1A2 variant associated with severe stepwise regression, hemiplegia, epilepsy and movement disorders in two unrelated patients.
Migraine with Aura
A novel lethal recognizable polymicrogyric syndrome caused by ATP1A2 homozygous truncating variants.
Migraine with Aura
A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2.
Migraine with Aura
Acute encephalopathy in familial hemiplegic migraine with ATP1A2 mutation.
Migraine with Aura
Alternating hemiplegia of childhood and a pathogenic variant of ATP1A3: a case report and pathophysiological considerations.
Migraine with Aura
Alternating hemiplegia of childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2.
Migraine with Aura
An Infant With Epilepsy and Recurrent Hemiplegia due to Compound Heterozygous Variants in ATP1A2.
Migraine with Aura
Analysis of amplicon-based NGS data from neurological disease gene panels: a new method for allele drop-out management.
Migraine with Aura
Analysis of chromosome 1 microsatellite markers and the FHM2-ATP1A2 gene mutations in migraine pedigrees.
Migraine with Aura
Astrocytes in Atp1a2-deficient heterozygous mice exhibit hyperactivity after induction of cortical spreading depression.
Migraine with Aura
ATP1A2 gene mutations are not present in two sisters with basilar-type migraine associated with menses.
Migraine with Aura
ATP1A2 Mutations in Migraine: Seeing through the Facets of an Ion Pump onto the Neurobiology of Disease.
Migraine with Aura
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.
Migraine with Aura
Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations.
Migraine with Aura
Biphasic neurovascular changes in prolonged migraine aura in familial hemiplegic migraine type 2.
Migraine with Aura
CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family report.
Migraine with Aura
Characteristics of cortical spreading depression and c-Fos expression in transgenic mice having a mutation associated with familial hemiplegic migraine 2.
Migraine with Aura
Clinical spectrum in three families with familial hemiplegic migraine type 2 including a novel mutation in the ATP1A2 gene.
Migraine with Aura
Differential effect of FHM2 mutation on synaptic plasticity in distinct hippocampal regions.
Migraine with Aura
Diverse functional consequences of mutations in the Na+/K+-ATPase alpha2-subunit causing familial hemiplegic migraine type 2.
Migraine with Aura
Early Treatment in Acute Severe Encephalopathy Caused by ATP1A2 Mutation of Familial Hemiplegic Migraine Type 2: Case Report and Literature Review.
Migraine with Aura
Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations.
Migraine with Aura
Enhanced susceptibility to cortical spreading depression in two types of Na
Migraine with Aura
Familial basilar migraine associated with a new mutation in the ATP1A2 gene.
Migraine with Aura
Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation.
Migraine with Aura
Familial hemiplegic migraine presenting as recurrent encephalopathy in a Native Indian family.
Migraine with Aura
Familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2.
Migraine with Aura
Familial Hemiplegic Migraine Type 3 (FHM3) With an SCN1A Mutation in a Chinese Family: A Case Report.
Migraine with Aura
Familial Hemiplegic Migraine with an ATP1A4 Mutation: Clinical Spectrum and Carbamazepine Efficacy.
Migraine with Aura
Familial Hemiplegic Migraine With Asymmetric Encephalopathy Secondary to ATP1A2 Mutation: A Case Series.
Migraine with Aura
Familial Hemiplegic Migraine with Severe Attacks: A New Report with ATP1A2 Mutation.
Migraine with Aura
First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine.
Migraine with Aura
Functional characterization of a novel C-terminal ATP1A2 mutation causing hemiplegic migraine and epilepsy.
Migraine with Aura
Functional correlation of ATP1A2 mutations with phenotypic spectrum: from pure hemiplegic migraine to its variant forms.
Migraine with Aura
Genetic effects of ATP1A2 in familial hemiplegic migraine type II and animal models.
Migraine with Aura
Genetic studies of Polish migraine patients: screening for causative mutations in four migraine-associated genes.
Migraine with Aura
Genetics of migraine: an update with special attention to genetic comorbidity.
Migraine with Aura
Genome-wide screen for modifiers of Na + /K + ATPase alleles identifies critical genetic loci.
Migraine with Aura
Genomewide significant linkage to migrainous headache on chromosome 5q21.
Migraine with Aura
Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2.
Migraine with Aura
Haplotype-based systematic association studies of ATP1A2 in migraine with aura.
Migraine with Aura
Impaired plasma membrane targeting or protein stability by certain ATP1A2 mutations identified in sporadic or familial hemiplegic migraine.
Migraine with Aura
Increased susceptibility to cortical spreading depression and epileptiform activity in a mouse model for FHM2.
Migraine with Aura
Inhibition of phosphorylation of na+,k+-ATPase by mutations causing familial hemiplegic migraine.
Migraine with Aura
Insights into the Pathology of the ?2-Na(+)/K(+)-ATPase in Neurological Disorders; Lessons from Animal Models.
Migraine with Aura
Kinetic alterations due to a missense mutation in the Na,K-ATPase alpha2 subunit cause familial hemiplegic migraine type 2.
Migraine with Aura
Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families.
Migraine with Aura
Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4.
Migraine with Aura
Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.
Migraine with Aura
Na+/K+-ATPase ? isoform deficiency results in distinct spreading depolarization phenotypes.
Migraine with Aura
New discoveries about the second gene for familial hemiplegic migraine, ATP1A2.
Migraine with Aura
Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions.
Migraine with Aura
Partially Reversible Cortical Metabolic Dysfunction in Familial Hemiplegic Migraine With Prolonged Aura.
Migraine with Aura
Physical mapping and characterization of the human Na,K-ATPase isoform, ATP1A4.
Migraine with Aura
Polymorphisms in migraine-associated gene, atp1a2, and ischemic stroke risk in a biracial population: the genetics of early onset stroke study.
Migraine with Aura
Pulmonary arterial hypertension in familial hemiplegic migraine with ATP1A2 channelopathy.
Migraine with Aura
Rare missense variants in ATP1A2 in families with clustering of common forms of migraine.
Migraine with Aura
Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine.
Migraine with Aura
Recurrent coma and fever in familial hemiplegic migraine type 2. A prospective 15-year follow-up of a large family with a novel ATP1A2 mutation.
Migraine with Aura
Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutation.
Migraine with Aura
The CACNA1A and ATP1A2 genes are not involved in dominantly inherited migraine with aura.
Migraine with Aura
The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families.
Migraine with Aura
The Influence of Na(+), K(+)-ATPase on Glutamate Signaling in Neurodegenerative Diseases and Senescence.
Migraine with Aura
The structure of the Na+,K+-ATPase and mapping of isoform differences and disease-related mutations.
Migraine with Aura
Toward a molecular genetic classification of familial hemiplegic migraine.
Migraine with Aura
Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine.
Migraine with Aura
Two novel functional mutations in the Na+,K+-ATPase alpha2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes.
Migraine with Aura
Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants.
Migraine with Aura
Variable manifestations of familial hemiplegic migraine associated with reversible cerebral edema in children.
Migraine with Aura
[Genetics of migraines: from ionic channels to single nucleotide polymorphisms?]
Migraine without Aura
Analysis of chromosome 1 microsatellite markers and the FHM2-ATP1A2 gene mutations in migraine pedigrees.
Migraine without Aura
Familial hemiplegic migraine mutations affect Na,K-ATPase domain interactions.
Mitochondrial Diseases
A De Novo Mutation in the Adenosine Triphosphatase (ATPase) 8 Gene in a Patient With Mitochondrial Disorder.
Monoclonal Gammopathy of Undetermined Significance
[The significance of the cytochemical adenosine triphosphatase reaction for the diagnosis of benign monoclonal gammopathy (author's transl)]
Mononeuropathies
Endoneurial ATPase activity in Tangier disease and other peripheral neuropathies.
Mouth Neoplasms
Modulatory Action of ?-Tocopherol on Erythrocyte Membrane Adenosine Triphosphatase against Radiation Damage in Oral Cancer.
Movement Disorders
A novel ATP1A2 variant associated with severe stepwise regression, hemiplegia, epilepsy and movement disorders in two unrelated patients.
Movement Disorders
Hypothermia-induced dystonia and abnormal cerebellar activity in a mouse model with a single disease-mutation in the sodium-potassium pump.
Movement Disorders
Implantation of Osmotic Pumps and Induction of Stress to Establish a Symptomatic, Pharmacological Mouse Model for DYT/PARK-ATP1A3 Dystonia.
Multiple Sclerosis
A novel mitochondrial DNA deletion producing progressive external ophthalmoplegia associated with multiple sclerosis.
Multiple Sclerosis
Na+- and K+-dependent adenosine triphosphatase changes in multiple sclerosis plaques.
Muscle Hypotonia
Ocular Hypotonia and Transient Decrease of Vision as a Consequence of Exposure to a Common Toad Poison.
Muscular Atrophy
Aerobic Exercise Recovers Disuse-induced Atrophy Through the Stimulus of the LRP130/PGC-1? Complex in Aged Rats.
Muscular Atrophy
[Effects of Ligustrazine and Radix Astragali on activities of myosin adenosine triphosphatase of soleus muscle and muscle atrophy in tail-suspended rats]
Muscular Atrophy
[The preventive effects of one herbal compound on activities of myosin adenosine triphosphatase of muscle fibers and muscle atrophy in tail-suspended rat].
Muscular Diseases
A novel mitochondrial DNA deletion producing progressive external ophthalmoplegia associated with multiple sclerosis.
Muscular Diseases
Crooked calf disease: a histological and histochemical examination of eight affected calves.
Muscular Dystrophies
Ouabain and erythrocyte-ghost adenosine triphosphatase. Effects in human muscular dystrophies.
Muscular Dystrophies
Sodium channel and sodium pump in normal and pathological muscles from patients with myotonic muscular dystrophy and lower motor neuron impairment.
Muscular Dystrophies
[Adenosine triphosphatase activities of the erythrocyte membrane in Duchenne's myodystrophy]
Muscular Dystrophies
[Sodium- and potassium-dependent adenosine triphosphatase of erythrocyte shadows in patients with Duchenne's myodystrophy]
Muscular Dystrophy, Duchenne
Effect of ouabain upon erythrocyte membrane adenosine triphosphatase in Duchenne muscular dystrophy.
Muscular Dystrophy, Duchenne
Erythrocyte cation-activated adenosine triphosphatases in Duchenne muscular dystrophy.
Muscular Dystrophy, Duchenne
Erythrocyte membrane (Ca/+ + Mg/+)-activated adenosine triphosphatase in Duchenne muscular dystrophy.
Muscular Dystrophy, Duchenne
Erythrocyte-ghost Ca2+-stimulated Mg2+-dependent adenosine triphosphatase in Duchenne muscular dystrophy.
Muscular Dystrophy, Duchenne
Specificity of biophysical and biochemical alterations in erythrocyte membranes in neurological disorders--Huntington's disease, Friedreich's ataxia, Alzheimer's disease, amyotrophic lateral sclerosis, and myotonic and duchenne muscular dystrophy.
Muscular Dystrophy, Duchenne
Superprecipitation and adenosine triphosphatase activity of myosin B in Duchenne muscular dystrophy.
Muscular Dystrophy, Duchenne
The effect of ouabain on erythrocyte adenosine triphosphatase activity in relation to cell age in vivo and Duchenne muscular dystrophy.
Muscular Dystrophy, Duchenne
The sodium pump of erythrocytes from patients with Duchenne muscular dystrophy: effect of ouabain on the active sodium flux and on (Na+, K+)ATPase.
Myalgia
Investigation of the relationships between different enzymes and postmortem duck muscle tenderization.
Myocardial Infarction
Characterization of a urinary bufodienolide Na+,K+-ATPase inhibitor in patients after acute myocardial infarction.
Myocardial Infarction
Immunofluorescent microscopy for the identification of human necrotic myocardium.
Myocardial Infarction
Noninvasive quantification of total sodium concentrations in acute reperfused myocardial infarction using 23Na MRI.
Myocardial Infarction
Polymorphisms in migraine-associated gene, atp1a2, and ischemic stroke risk in a biracial population: the genetics of early onset stroke study.
Myocardial Infarction
Pretreatment with morin, a flavonoid, ameliorates adenosine triphosphatases and glycoproteins in isoproterenol-induced myocardial infarction in rats.
Myocardial Infarction
Preventive effect of naringin on isoproterenol-induced cardiotoxicity in Wistar rats: an in vivo and in vitro study.
Myocardial Infarction
Preventive effect of S-allylcysteine on membrane-bound enzymes and glycoproteins in normal and isoproterenol-induced cardiac toxicity in male Wistar rats.
Myocardial Infarction
Protective effect of Lagenaria siceraria (Mol) against membrane-bound enzyme alterations in isoproterenol-induced cardiac damage in rats.
Myocardial Infarction
The ?2-isoform of the Na+/K+-ATPase protects against pathological remodeling and ?-adrenergic desensitization after myocardial infarction.
Myocardial Ischemia
Alleviation of isoprenaline hydrochloride induced myocardial ischemia injury by brucine through the inhibition of Na+/K+-ATPase.
Myocardial Ischemia
Benzodiazepine-based selective inhibitors of mitochondrial F1F0 ATP hydrolase.
Myocardial Ischemia
Calpain-mediated impairment of Na+/K+-ATPase activity during early reperfusion contributes to cell death after myocardial ischemia.
Myocardial Ischemia
Pharmacological profile of the selective mitochondrial F1F0 ATP hydrolase inhibitor BMS-199264 in myocardial ischemia.
Myocardial Ischemia
[Study of the calmodulin-dependent regulation of calcium adenosine triphosphatase of erythrocyte membranes in patients with ischemic heart disease]
Myocardial Ischemia
[The effect of laser irradiation of the blood on the adenosine triphosphatase activity of the erythrocyte membranes and on the cardiac activity indices in patients with ischemic heart disease]
Myocardial Reperfusion Injury
Antidigoxin antiserum prevents endogenous digitalis-like compound-mediated reperfusion injury via modulating sodium pump isoform gene expression.
Myocardial Stunning
Lack of the effect of superoxide dismutase and catalase on Na+,K+-ATPase activity in stunned rabbit hearts.
Myocarditis
[The catecholamine concentration and adenosine triphosphatase activity of the myocardium in experimental myocarditis]
Myopia
Disrupted potassium ion homeostasis in ciliary muscle in negative lens-induced myopia in Guinea pigs.
Myotonia
Diazacholesterol myotonia: accumulation of desmosterol and increased adenosine triphosphatase activity of sarcolemma.
Myotonia
Membrane desmosterol and the kinetics of the sarcolemmal Na+,K+-ATPase in myotonia induced by 20,25-diazacholesterol.
Myotonic Dystrophy
Localization of a human Na+,K+-ATPase alpha subunit gene to chromosome 19q12----q13.2 and linkage to the myotonic dystrophy locus.
Neoplasm Metastasis
Identification and cloning of genes displaying elevated expression as a consequence of metastatic progression in human melanoma cells by rapid subtraction hybridization.
Neoplasms
(3H)ouabain binding to leukaemic cells and intralymphocytic sodium content in chronic lymphocytic leukaemia; no evidence for alterations of the Na+/K+-pump.
Neoplasms
2.3 Å resolution cryo-EM structure of human p97 and mechanism of allosteric inhibition.
Neoplasms
A comparative study of inner membrane enzymes and transport systems in mitochondria from R3230AC mammary tumor and normal rat mammary gland.
Neoplasms
A cytochemical study on the salivary gland pleomorphic adenoma (mixed tumor) and the fetal and adult salivary gland.
Neoplasms
A distinctive cutaneous malignant neoplasm expressing the Langerhans cell phenotype. Synchronous occurrence with B-chronic lymphocytic leukemia.
Neoplasms
A Mg2+- and Ca2+-stimulated adenosine triphosphatase at the outer surface of Ehrlich ascites tumor cells.
Neoplasms
A near-infrared light-controlled, ultrasensitive one-step photoelectrochemical detection of dual cell apoptosis indicators in living cancer cells.
Neoplasms
A new water-soluble polythiophene derivative as a probe for real-time monitoring adenosine 5'-triphosphatase activity in lysosome of living cells.
Neoplasms
Activation and proliferation signals in murine macrophages: stimulation of Na+,K+-ATPase activity by hemopoietic growth factors and other agents.
Neoplasms
Activation of novel estrogen receptor GPER results in inhibition of cardiocyte apoptosis and cardioprotection.
Neoplasms
Alteration by phenobarbital of membrane-associated enzymes including gamma glutamyl transpeptidase in mouse liver neoplasms.
Neoplasms
An electron cytochemical demonstration and biochemical analysis of adenosine triphosphatase activity in cancer cell plasma membrane.
Neoplasms
An evaluation of enzyme histochemistry in the diagnosis of childhood rhabdomyosarcoma.
Neoplasms
Anti-inflammatory effects induced by pharmaceutical substances on inflammatory active brain astrocytes-promising treatment of neuroinflammation.
Neoplasms
Anticancer ruthenium(III) complex KP1019 interferes with ATP-dependent Ca2+ translocation by sarco-endoplasmic reticulum Ca2+-ATPase (SERCA).
Neoplasms
ARID1A immunohistochemistry improves outcome prediction in invasive urothelial carcinoma of urinary bladder.
Neoplasms
Association of ATP7A expression and in vitro sensitivity to cisplatin in non-small cell lung cancer.
Neoplasms
ATP6AP2 is Overexpressed in Breast Cancer and Promotes Breast Cancer Progression.
Neoplasms
ATP7B expression is associated with in vitro sensitivity to cisplatin in non-small cell lung cancer.
Neoplasms
ATPase inhibitory factor 1 is a potential prognostic marker for the migration and invasion of glioma.
Neoplasms
Bilirubin attenuates bufadienolide-induced ventricular arrhythmias and cardiac dysfunction in Guinea-pigs by reducing elevated intracellular na(+) levels.
Neoplasms
Bone marrow-infiltrating human neuroblastoma cells express high levels of calprotectin and HLA-G proteins.
Neoplasms
BRIP1 inhibits the tumorigenic properties of cervical cancer by regulating RhoA GTPase activity.
Neoplasms
Cancer mortality does not differ by antiarrhythmic drug use: A population-based cohort of Finnish men.
Neoplasms
Cardenolide-induced lysosomal membrane permeabilization demonstrates therapeutic benefits in experimental human non-small cell lung cancers.
Neoplasms
Cardiac glycoside bufalin blocks cancer cell growth by inhibition of Aurora A and Aurora B activation via PI3K-Akt pathway.
Neoplasms
Cardiac Glycoside Ouabain Exerts Anticancer Activity via Downregulation of STAT3.
Neoplasms
Cardiotonic Steroids-Mediated Na+/K+-ATPase Targeting Could Circumvent Various Chemoresistance Pathways.
Neoplasms
Cardiotonic Steroids-Mediated Targeting of the Na(+)/K(+)-ATPase to Combat Chemoresistant Cancers.
Neoplasms
Cinobufagin Triggers Defects in Spindle Formation and Cap-Dependent Translation in Liver Cancer Cells by Inhibiting the AURKA-mTOR-eIF4E Axis.
Neoplasms
Crosstalk between Na+,K+-ATPase and a volume-regulated anion channel in membrane microdomains of human cancer cells.
Neoplasms
Cytotoxicity of AMANTADIG - a semisynthetic digitoxigenin derivative - alone and in combination with docetaxel in human hormone-refractory prostate cancer cells and its effect on Na+/K+-ATPase inhibition.
Neoplasms
Different roles of proteolipids and 70-kDa subunits of V-ATPase in growth and death of cultured human cells.
Neoplasms
Differential sensitivity of human gastric cancer ATPase and normal gastric mucosa ATPase to the synthetic mammalian lignan analogue 2,3-dibenzylbutane-1,4-diol (hattalin).
Neoplasms
Downregulation of RUVBL1 inhibits proliferation of lung adenocarcinoma cells by G1/S phase cell cycle arrest via multiple mechanisms.
Neoplasms
Early uptake and continuous accumulation of thallium-201 chloride in a benign mixed tumor of soft tissue: Case Report.
Neoplasms
Ecto-enzymes of mammary gland and its tumours. Ca2+- or Mg2+-stimulated adenosine triphosphatase and its perturbation by concanavalin A.
Neoplasms
Editorial: on the road to multi-modal and pluri-disciplinary treatment of glioblastomas.
Neoplasms
Effect of Ginkgo biloba extract 50 on immunity and antioxidant enzyme activities in ischemia reperfusion rats.
Neoplasms
Engineering a prostate-specific membrane antigen-activated tumor endothelial cell prodrug for cancer therapy.
Neoplasms
Enhancing the anticancer properties of cardiac glycosides by neoglycorandomization.
Neoplasms
Evaluation of the relationship of erythrocyte membrane Na+/K+-ATPase enzyme activity and tumor response to chemoradiotherapy in patients diagnosed with locally advanced nonsmall cell lung cancer and glioblastoma multiforme.
Neoplasms
Experimental evaluation of the usefulness of 201Tl-chloride scintigraphy for monitoring radiotherapeutic effects.
Neoplasms
Expression of ATP7A in esophageal squamous cell carcinoma (ESCC) and its clinical significance.
Neoplasms
Expression of the copper transporters hCtr1, ATP7A and ATP7B is associated with the response to chemotherapy and survival time in patients with resected non-small cell lung cancer.
Neoplasms
Family of Na+,K+-ATPase genes. Intra-individual tissue-specific restriction fragment length polymorphism.
Neoplasms
Hellebrin and its aglycone form hellebrigenin display similar in vitro growth inhibitory effects in cancer cells and binding profiles to the alpha subunits of the Na+/K+-ATPase.
Neoplasms
Hepatoprotective effect of Caesalpinia gilliesii and Cajanus cajan proteins against acetoaminophen overdose-induced hepatic damage.
Neoplasms
Hepatoprotective potential of standardized Ficus species in intrahepatic cholestasis rat model: Involvement of nuclear factor-?B, and Farnesoid X receptor signaling pathways.
Neoplasms
Histopathological and Immunohistochemical Characterization of Methyl Eugenol-induced Nonneoplastic and Neoplastic Neuroendocrine Cell Lesions in Glandular Stomach of Rats.
Neoplasms
Hypotheses about sub-optimal hydration in the weeks before coronavirus disease (COVID-19) as a risk factor for dying from COVID-19.
Neoplasms
Identification of a sodium pump Na+/K+ ATPase ?1-targeted peptide for PET imaging of breast cancer.
Neoplasms
Immune and enzyme histochemical studies of a human hepatocellular carcinoma cell line producing hepatitis B surface antigen.
Neoplasms
Impairment of sodium pump and Na+/H+ antiport in erythrocytes isolated from cancer patients.
Neoplasms
Increase in adenosine triphosphatase activity of Ehrlich ascites tumor cells following serial cultivation in media with increased (hypertonic) NaCl content.
Neoplasms
Inhibition of the sodium potassium adenosine triphosphatase pump sensitizes cancer cells to anoikis and prevents distant tumor formation.
Neoplasms
Intracellular accumulation of thallium as a marker of cisplatin cytotoxicity in nonsmall cell lung carcinoma: an application of inductively coupled plasma mass spectrometry.
Neoplasms
Investigation of dose-dependent effects of berberine against renal ischemia/reperfusion injury in experimental diabetic rats.
Neoplasms
Mitophagy Induced by Mitochondrial Function Damage in Chicken Kidney Exposed to Cr(VI).
Neoplasms
Morphologic and cytochemical properties of mouse liver neoplasms induced by diethylnitrosamine and promoted by 4,4'-dichlorodiphenyltrichloroethane, chlordane, or heptachlor.
Neoplasms
Na+/K+-ATPase Revisited: On Its Mechanism of Action, Role in Cancer, and Activity Modulation.
Neoplasms
Na+/K+-ATPase-Targeted Cytotoxicity of (+)-Digoxin and Several Semisynthetic Derivatives.
Neoplasms
Nonspecifically enhanced therapeutic effects of vincristine on multidrug-resistant cancers when coencapsulated with quinine in liposomes.
Neoplasms
One-megabase yeast artificial chromosome and 400-kilobase cosmid-phage contigs containing the von Hippel-Lindau tumor suppressor and Ca(2+)-transporting adenosine triphosphatase isoform 2 genes.
Neoplasms
Oxidative Stress and Apoptotic Responses Elicited by Nostoc-Synthesized Silver Nanoparticles against Different Cancer Cell Lines.
Neoplasms
Plumbagin-induced oxidative stress leads to inhibition of Na+/K+-ATPase (NKA) in canine cancer cells.
Neoplasms
Polyamines secreted by cancer cells possibly account for the impairment of the human erythrocyte sodium pump activity.
Neoplasms
Primary rhabdomyosarcoma of the cerebellum--a light, electron microscopic, and immunohistochemical study.
Neoplasms
Quantification of ATP-producing and consuming processes of Ehrlich ascites tumour cells.
Neoplasms
Rabeprazole exhibits antiproliferative effects on human gastric cancer cell lines.
Neoplasms
Sodium pump and Na+/H+ antiport restoration in erythrocytes from cancer patients in remission.
Neoplasms
Steroid Glycosides Hyrcanoside and Deglucohyrcanoside: On Isolation, Structural Identification, and Anticancer Activity.
Neoplasms
Structural Insights into the Interactions of Digoxin and Na+/K+-ATPase and Other Targets for the Inhibition of Cancer Cell Proliferation.
Neoplasms
Suppressor cell activation and enhanced skin allograft survival after tumor promotor but not initiator induced depletion of cutaneous Langerhans cells.
Neoplasms
Survival of detached cancer cells is regulated by movement of intracellular Na+,K+-ATPase.
Neoplasms
Targeting FXYD2 by cardiac glycosides potently blocks tumor growth in ovarian clear cell carcinoma.
Neoplasms
Thallium-201 chloride (Tl-201) accumulation and Na+/K+-ATPase expression in tumours of the head and neck.
Neoplasms
The Effect of Curcumin Nanoparticles on Cisplatin-Induced Cardiotoxicity in Male Wistar Albino Rats.
Neoplasms
The expression of the alpha1 subunit of Na+/K+-ATPase is related to tumor development and clinical outcomes in gastric cancer.
Neoplasms
The fine structural localisation of thiamine pyrophosphatase and adenosine triphosphatase in neural tumours induced by N-ethyl-N-nitrosourea in rats.
Neoplasms
The Sodium Pump alpha1 Subunit: a Disease Progression-Related Target for Metastatic Melanoma Treatment.
Neoplasms
The vacuolar-type ATPase inhibitor archazolid increases tumor cell adhesion to endothelial cells by accumulating extracellular collagen.
Neoplasms
Transgenic overexpression of translationally controlled tumor protein induces systemic hypertension via repression of Na+,K+-ATPase.
Neoplasms
Tumor-associated a2 vacuolar ATPase acts as a key mediator of cancer-related inflammation by inducing pro-tumorigenic properties in monocytes.
Neoplasms
Tumour blood flow for prediction of human prostate cancer aggressiveness: a study with Rubidium-82 PET, MRI and Na+/K+-ATPase-density.
Neoplasms
Ultrastructural and cytochemical studies on hyperbasophilic foci with special reference to the demonstration of cell surface alterations in hepatocarcinogenesis.
Neoplasms
Ultrastructural localization of membrane phosphatases in teratocarcinoma and early embryos.
Neoplasms
UNBS1450 from Calotropis procera as a regulator of signaling pathways involved in proliferation and cell death.
Neoplasms
Uncoupler-stimulated adenosine triphosphatase activity. Deficiency in intact mitochondria from Morris hepatomas and ascites tumor cells.
Neoplasms
Update on the effects of the sodium pump ?1 subunit on human glioblastoma: from the laboratory to the clinic.
Neoplasms
[A Simple Medical Research Microdevice for Analyzing Three-dimensional Migration of Tumor Cells in Vitro].
Neoplasms
[Action of thymic lipid extract B on adenosine triphosphatase and succinate dehydrogenase of the liver of rats with Guerin tumors]
Neoplasms
[Cancer cell-specific functional relation between Na+,K+-ATPase and volume-regulated anion channel].
Neoplasms
[Cytomorphological and enzyme histological studies of bilaterally inoculated Dibromdulcit-sensitive and-resistent Yoshida tumors]
Neoplasms
[Differential expression of 2 genes of the Na+,K+-AtPase subunit in normal and tumor tissues in humans]
Neoplasms
[Histochemical and ultrastructural investigations on organ culture of malignant tumors (author's transl)]
Neoplasms
[HISTOCHEMICAL DEMONSTRATION OF ADENOSINE TRIPHOSPHATASE ACTIVITY IN TRANSPLANTABLE TUMORS AND CORRESPONDING NORMAL TISSUES.]
Neoplasms
[Photodynamic effect of a hematoporphyrin derivative on the sodium pump activity and aerobic glycolysis in tumor cells]
Neoplasms
[Significance of the inhibition of adenosine triphosphatase of the red splenic pulp during the development of tumor transplants in rats]
Neoplasms
[Ultracytochemical study of the nucleoside phosphatase activity of nuclei of epithelial cells of the gastric mucosa and of stomach cancer cells in humans]
Nephritis
Glomerulonephritis and sodium retention: enhancement of Na+/K+-ATPase activity in the collecting duct is shared by rats with puromycin induced nephrotic syndrome and mice with spontaneous lupus-like glomerulonephritis.
Nephrosis
Hyperaldosteronemia and activation of the epithelial sodium channel are not required for sodium retention in puromycin-induced nephrosis.
Nephrosis
OBSERVATIONS OF RAT KIDNEY MITOCHONDRIAL ADENOSINE TRIPHOSPHATASE ACTIVITY DURING INDUCTION OF AMINONUCLEOSIDE NEPHROSIS.
Nephrotic Syndrome
Glomerulonephritis and sodium retention: enhancement of Na+/K+-ATPase activity in the collecting duct is shared by rats with puromycin induced nephrotic syndrome and mice with spontaneous lupus-like glomerulonephritis.
Nephrotic Syndrome
Hyperaldosteronemia and activation of the epithelial sodium channel are not required for sodium retention in puromycin-induced nephrosis.
Nephrotic Syndrome
Nephrotic syndrome: new concepts in the pathophysiology of sodium retention.
Nephrotic Syndrome
[Cellular and molecular mechanisms of sodium pump activation in experimental models of nephrotic syndrome]
Nervous System Diseases
A novel mitochondrial ATPase 6 point mutation in familial bilateral striatal necrosis.
Nervous System Diseases
Asparagine-905 of the mammalian phospholipid flippase ATP8A2 is essential for lipid substrate-induced activation of ATP8A2 dephosphorylation.
Nervous System Diseases
Decreased content of ascorbic acid (vitamin C) in the brain of knockout mouse models of Na+,K+-ATPase-related neurologic disorders.
Nervous System Diseases
Insights into the Pathology of the ?2-Na(+)/K(+)-ATPase in Neurological Disorders; Lessons from Animal Models.
Nervous System Diseases
Short-term block of Na+/K+-ATPase in neuro-glial cell cultures of cerebellum induces glutamate dependent damage of granule cells.
Nervous System Diseases
Specificity of biophysical and biochemical alterations in erythrocyte membranes in neurological disorders--Huntington's disease, Friedreich's ataxia, Alzheimer's disease, amyotrophic lateral sclerosis, and myotonic and duchenne muscular dystrophy.
Nervous System Diseases
The Influence of Na(+), K(+)-ATPase on Glutamate Signaling in Neurodegenerative Diseases and Senescence.
Neuroblastoma
Acute changes in myo-inositol uptake and 22Na+ flux in murine neuroblastoma cells (N1E-115) following insulin.
Neuroblastoma
Alterations of membrane integrity and cellular constituents by arachidonic acid in neuroblastoma and glioma cells.
Neuroblastoma
Cilostazol, a cyclic AMP phosphodiesterase inhibitor, stimulates nitric oxide production and sodium potassium adenosine triphosphatase activity in SH-SY5Y human neuroblastoma cells.
Neuroblastoma
Membrane regulation of the Na+,K+-ATPase during the neuroblastoma cell cycle: correlation with protein lateral mobility.
Neuroblastoma
Reversal of hyperglycemic-induced defects in myo-inositol metabolism and Na+/K+ pump activity in cultured neuroblastoma cells by normalizing glucose levels.
Neuroblastoma
Sodium pump alpha1 and alpha3 subunit isoforms mediate distinct responses to ouabain and are both essential for survival of human neuroblastoma.
Neuroblastoma
Stimulation of the membrane-bound, magnesium-dependent adenosine triphosphatase of mouse neuroblastoma by concanavalin A and wheat germ agglutinin.
Neuroblastoma
The chronic and acute effects of ethanol on adenosine triphosphatase activity in cultured astroblast and neuroblastoma cells.
Neuroblastoma
[Rapid simultaneous isolation of microsomes and plasma membranes from neuroblastoma C 1300 N 18 cells]
Neurodegenerative Diseases
ATP7A (Menkes protein) functions in axonal targeting and synaptogenesis.
Neurodegenerative Diseases
ATP7A gene addition to the choroid plexus results in long-term rescue of the lethal copper transport defect in a Menkes disease mouse model.
Neurodegenerative Diseases
Copper homeostasis in the CNS: a novel link between the NMDA receptor and copper homeostasis in the hippocampus.
Neurodegenerative Diseases
Functional expression of the menkes disease protein reveals common biochemical mechanisms among the copper-transporting P-type ATPases.
Neurodegenerative Diseases
In vitro studies of the influence of glutamatergic agonists on the Na+,K+-ATPase and K+-p-nitrophenylphosphatase activities in the hippocampus and frontal cortex of rats.
Neurodegenerative Diseases
L-Threo-Dihydroxyphenylserine corrects neurochemical abnormalities in a menkes disease mouse model.
Neurodegenerative Diseases
Multi-angle development of therapeutic methods for Alzheimer's disease.
Neurodegenerative Diseases
Possible involvement of membrane lipids peroxidation and oxidation of catalytically essential thiols of the cerebral transmembrane sodium pump as component mechanisms of iron-mediated oxidative stress-linked dysfunction of the pump's activity.
Neurodegenerative Diseases
Safety of intracerebroventricular copper histidine in adult rats.
Neuroinflammatory Diseases
The ?2 Na+/K+-ATPase isoform mediates LPS-induced neuroinflammation.
Neuronal Ceroid-Lipofuscinoses
Atp13a2-deficient mice exhibit neuronal ceroid lipofuscinosis, limited ?-synuclein accumulation and age-dependent sensorimotor deficits.
Newcastle Disease
Adenosine triphosphatase associated with Newcastle disease virus. Conditions for its optimum activity.
Non-alcoholic Fatty Liver Disease
Phenotypic Alteration of Hepatocytes in Non-Alcoholic Fatty Liver Disease.
Obesity
A reproducible procedure for measuring sodium transport in cultured human fibroblasts from normal and obese donors.
Obesity
Effects of obesity and estradiol on Na+/K+-ATPase and their relevance to cardiovascular diseases.
Obesity
Erythrocyte sodium-potassium-stimulated adenosine triphosphatase activity is not related to obesity.
Obesity
Reduced Na+, K+ -ATPase activity in intact red cells and isolated membranes from obese man.
Obesity
The Cardiotonic Steroid Marinobufagenin Is a Predictor of Increased Left Ventricular Mass in Obesity: The African-PREDICT Study.
Obesity
The effect of oral glucose on the leucocyte sodium pump in normal and obese subjects.
Obesity
Transactivation of epidermal growth factor receptor in vascular and renal systems in rats with experimental hyperleptinemia: role in leptin-induced hypertension.
Obesity
Two-dimensional, sex-specific autosomal linkage scan of the number of sodium pump sites.
Obstetric Labor, Premature
Alterations in uterine sodium pump abundance may contribute to the onset and progression of term and preterm labor in mice.
Oligospermia
Reduced activity of Mg2+- and Ca2+-dependent adenosine triphosphatase in seminal fluid of patients with oligozoospermia.
Ophthalmoplegia, Chronic Progressive External
A novel mitochondrial DNA deletion producing progressive external ophthalmoplegia associated with multiple sclerosis.
Optic Atrophy
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.
Optic Atrophy
The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management.
Optic Atrophy
The Influence of Na(+), K(+)-ATPase on Glutamate Signaling in Neurodegenerative Diseases and Senescence.
Osteoarthritis
Decreased NA+, K+-ATPase activity in erythrocyte membrane from rheumatoid arthritis patients.
Osteoarthritis
The effects of osteoarthritis and age on skeletal muscle strength, Na+,K+-ATPase content, gene and isoform expression.
Osteosarcoma
Human osteogenic sarcoma: fine structural localization of adenosine triphosphatase.
Overweight
Leucocyte sodium content and sodium pump activity in overweight and lean hypertensives.
Overweight
Peculiarities of the effects of bile acids on atpase activity of the colon mucosa in patients with overweight and irritable bowel syndrome.
Overweight
The sodium pump and energy regulation: some new aspects for essential hypertension, diabetes II and severe overweight.
p-type na+ transporter deficiency
Exertional rhabdomyolysis in a patient with calcium adenosine triphosphatase deficiency.
p-type na+ transporter deficiency
Physiological suppression of a transport defect in Escherichia coli mutants deficient in Ca2+, Mg2+-stimulated adenosine triphosphatase.
p-type na+ transporter deficiency
Renal sodium- and potassium-activated adenosine triphosphatase deficiency during post-obstructive diuresis in the rat.
p-type na+ transporter deficiency
Sarcoplasmic reticulum adenosine triphosphatase deficiency with probable autosomal dominant inheritance.
p-type phospholipid transporter deficiency
Assessment of Adenosine Triphosphatase Phospholipid Transporting 8B1 (ATP8B1) Function in Patients With Cholestasis With ATP8B1 Deficiency by Using Peripheral Blood Monocyte-Derived Macrophages.
p-type phospholipid transporter deficiency
Folding defects in P-type ATP 8B1 associated with hereditary cholestasis are ameliorated by 4-phenylbutyrate.
p-type phospholipid transporter deficiency
In-silico Evaluation of Rare Codons and their Positions in the Structure of ATP8b1 Gene.
Pancreatitis, Chronic
Immunohistochemical localization of Na+, K+-ATPase in human normal and malignant pancreatic tissues.
Paralysis
A mutation of the Drosophila sodium pump alpha subunit gene results in bang-sensitive paralysis.
Paralysis
A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms.
Paralysis
Arg16Gly polymorphism in beta2-adrenergic receptor gene is not associated with thyrotoxic periodic paralysis in Korean male patients with Graves' disease.
Paralysis
In vivo and in vitro sodium pump activity in subjects with thyrotoxic periodic paralysis.
Paralysis
Intratympanic steroid injection as a first-line therapy in uremia patients with sudden sensorineural hearing loss.
Paramyxoviridae Infections
Na+/K+-ATPase as a Target of Cardiac Glycosides for the Treatment of SARS-CoV-2 Infection.
Parkinson Disease
Analysis of amplicon-based NGS data from neurological disease gene panels: a new method for allele drop-out management.
Parkinson Disease
Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease.
Parkinson Disease
Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration.
Parkinson Disease
Parkinson's disease-associated human ATP13A2 (PARK9) deficiency causes zinc dyshomeostasis and mitochondrial dysfunction.
Parkinson Disease
Protection against Mitochondrial and Metal Toxicity Depends on Functional Lipid Binding Sites in ATP13A2.
Parkinson Disease
Quinone and oxyradical scavenging properties of N-acetylcysteine prevent dopamine mediated inhibition of Na+, K+-ATPase and mitochondrial electron transport chain activity in rat brain: implications in the neuroprotective therapy of Parkinson's disease.
Parkinsonian Disorders
ATP13A2 deficiency induces a decrease in cathepsin D activity, fingerprint-like inclusion body formation, and selective degeneration of dopaminergic neurons.
Parkinsonian Disorders
ATP13A2 regulates mitochondrial bioenergetics through macroautophagy.
Parkinsonian Disorders
Characterization of cellular protective effects of ATP13A2/PARK9 expression and alterations resulting from pathogenic mutants.
Parkinsonian Disorders
Common pathogenic effects of missense mutations in the P-type ATPase ATP13A2 (PARK9) associated with early-onset parkinsonism.
Parkinsonian Disorders
Genome-wide screen for modifiers of Na + /K + ATPase alleles identifies critical genetic loci.
Parkinsonian Disorders
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase.
Parkinsonian Disorders
Hypothermia-induced dystonia and abnormal cerebellar activity in a mouse model with a single disease-mutation in the sodium-potassium pump.
Parkinsonian Disorders
Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration.
Parkinsonian Disorders
Mutations Phe785Leu and Thr618Met in Na+,K+-ATPase, associated with familial rapid-onset dystonia parkinsonism, interfere with Na+ interaction by distinct mechanisms.
Parkinsonian Disorders
Pathogenic effects of novel mutations in the P-type ATPase ATP13A2 (PARK9) causing Kufor-Rakeb syndrome, a form of early-onset parkinsonism.
Parkinsonian Disorders
Protection against Mitochondrial and Metal Toxicity Depends on Functional Lipid Binding Sites in ATP13A2.
Parkinsonian Disorders
Rescue of Na+ Affinity in Aspartate-928 Mutants of Na+,K+-ATPase by Secondary Mutation of Glutamate-314.
Parkinsonian Disorders
Sodium Pumps Mediate Activity-Dependent Changes in Mammalian Motor Networks.
Parkinsonian Disorders
The structure of the Na+,K+-ATPase and mapping of isoform differences and disease-related mutations.
Pemphigus
[Adenosine triphosphatase activity in human skin under normal conditions and in chronic pemphigus]
Peptic Ulcer
Treatment of refractory peptic ulcer with omeprazole or continued H2 receptor antagonists: a controlled clinical trial.
Periapical Periodontitis
Apical periodontitis induces changes on oxidative stress parameters and increases Na+/K+-ATPase activity in adult rats.
Periodontitis
Comparative analysis of the effects of a novel vacuolar adenosine 5'-triphosphatase inhibitor, FR202126, and doxycycline on bone loss caused by experimental periodontitis in rats.
Peripheral Nervous System Diseases
Endoneurial ATPase activity in Tangier disease and other peripheral neuropathies.
Phenylketonurias
Alanine prevents the decrease of Na+,K+-ATPase activity in experimental phenylketonuria.
Phenylketonurias
Effects of L-phenylalanine on acetylcholinesterase and Na+,K+-ATPase activities in suckling rat frontal cortex, hippocampus and hypothalamus.
Phenylketonurias
Effects of phenylalanine and its deaminated metabolites on Na+,K+-ATPase activity in synaptosomes from rat brain.
Phenylketonurias
In vivo effects of high phenylalanine blood levels on Na+,K+-ATPase, Mg2+-ATPase activities and biogenic amine concentrations in phenylketonuria.
Photosensitivity Disorders
The effect of hypericin and hypocrellin-A on lipid membranes and membrane potential of 3T3 fibroblasts.
Placental Insufficiency
Complex, coordinated and highly regulated changes in placental signaling and nutrient transport capacity in IUGR.
Plasmacytoma
Specific involvement of calmodulin and non-specific effect of tropomyosin in the sensitivity to ouabain of Na+,K+-ATPase in murine plasmocytoma cells.
Plasmacytoma
[Diagnosis of plasmocytoma using the adenosine triphosphatase reaction on bone marrow smears]
Plasmacytoma
[The cutologic diagnosis of a plasmacytoma of a bone marrow smear by means of the adenosine triphosphatase reaction]
Pneumonia
Dynamic regulation of cardiolipin by the lipid pump Atp8b1 determines the severity of lung injury in experimental pneumonia.
Pneumonia
Pulmonary inflammation and edema induced by phospholipase A2: global gene analysis and effects on aquaporins and Na+/K+-ATPase.
Pneumoperitoneum
The effects of sevoflurane and propofol anesthesia on renal sodium-potassium adenosine triphosphatase activity during pneumoperitoneum in rats.
Polycystic Kidney Diseases
A role for Na/K adenosine triphosphatase in the pathogenesis of cyst formation in experimental polycystic kidney disease.
Polycystic Kidney Diseases
Abnormal sodium pump distribution during renal tubulogenesis in congenital murine polycystic kidney disease.
Polycystic Kidney Diseases
Sodium pump distribution is not reversed in the DBA/2FG-pcy, polycystic kidney disease model mouse.
Polycystic Kidney Diseases
[Progressive reduction of alkaline phosphatase and of Mg-dependent adenosine triphosphatase (Mg-ATPase) in congenital polycystic kidney in PM/Se mice]
Polymicrogyria
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.
Polyuria
The pathophysiology of septic shock: acute renal failure in rats following live E coli injection. A histochemical study of the proximal tubules.
Porcine Reproductive and Respiratory Syndrome
The effect of porcine reproductive and respiratory syndrome virus and porcine epidemic diarrhea virus challenge on growing pigs II: Intestinal integrity and function.
Potassium Deficiency
Adaptation of the cardiac muscle sodium pump to chronic potassium deficiency.
Pre-Eclampsia
Circulating bufodienolide and cardenolide sodium pump inhibitors in preeclampsia.
Pre-Eclampsia
Digibind Reverses Inhibition of Cellular rb+ Uptake Caused by Endogenous Sodium Pump Inhibitors Present in Serum and Placenta of Women With Preeclampsia.
Pre-Eclampsia
Digoxin Immune Fab Protects Endothelial Cells from Ouabain-Induced Barrier Injury.
Pre-Eclampsia
Endogenous sodium pump inhibitors, diabetes mellitus and preeclampsia Preliminary observations and a hypothesis.
Pre-Eclampsia
Leucocyte electrolytes and sodium efflux rate constants in the hypertension of pre-eclampsia.
Pre-Eclampsia
Preeclampsia and calcium adenosine triphosphatase activity of red blood cell ghosts.
Pre-Eclampsia
Preeclampsia, lipid peroxidation, and calcium adenosine triphosphatase activity of red blood cell ghosts.
Pre-Eclampsia
Sodium regulation, sodium pump function and sodium pump inhibitors in uncomplicated pregnancy and preeclampsia.
Pregnancy, Prolonged
[Accumulation of actomyosin and its adenosine triphosphatase activity in the muscle of cervix uteri in prolonged pregnancy]
Pressure Ulcer
[Activity of adenosine triphosphatase and the expression of ryanodine receptor 1 mRNA in local tissue of pressure ulcer at early stage in gracilis of rats].
Prostatic Hyperplasia
[Enzymatic activities in human prostatic adenoma (leucine aminopeptidase, 5-nucleotidase, adenosine triphosphatase, lactic dehydrogenase, phosphohexoisomerase).]
Prostatic Neoplasms
Cytotoxicity of AMANTADIG - a semisynthetic digitoxigenin derivative - alone and in combination with docetaxel in human hormone-refractory prostate cancer cells and its effect on Na+/K+-ATPase inhibition.
Prostatic Neoplasms
Regulation of expression of Na+,K+-ATPase in androgen-dependent and androgen-independent prostate cancer.
Protein-Energy Malnutrition
Erythrocyte membrane Na+ and K+ activated adenosine triphosphatase in protein-calorie malnutrition.
Protein-Energy Malnutrition
Erythrocyte osmotic fragility in protein-energy malnutrition: cholesterol, phospholipid, and CA2+, Mg2+ adenosine triphosphatase.
Protein-Energy Malnutrition
Modified kinetics of erythrocyte membrane Na+-K+ adenosine triphosphatase in protein-energy malnutrition.
Protein-Energy Malnutrition
Oedema in protein energy malnutrition: the role of the sodium pump.
Pseudohypoaldosteronism
Erythrocyte Na+,K+-ATPase and nasal potential in pseudohypoaldosteronism.
Pulmonary Arterial Hypertension
Pulmonary arterial hypertension in familial hemiplegic migraine with ATP1A2 channelopathy.
Pulmonary Disease, Chronic Obstructive
The heavy metal tolerant soil bacterium Achromobacter sp. AO22 contains a unique copper homeostasis locus and two mer operons.
Pulmonary Disease, Chronic Obstructive
[Reduced expression of the sarcoplasmic calcium pump SERCA2 in skeletal muscle from patients with chronic obstructive pulmonary disease and low body weight]
Pulmonary Edema
Modulation of pulmonary NA+ pump gene expression during cold storage and reperfusion.
Pulmonary Edema
Single dexamethasone injection increases alveolar fluid clearance in adult rats.
Pulmonary Sclerosing Hemangioma
Sclerosing hemangioma of the lung. An immunohistochemical study of intermediate filaments and endothelial markers.
Renal Insufficiency
A labile sodium pump inhibitor from the peritoneal dialysate of hypertensive renal failure patients: estimates of potency.
Renal Insufficiency
Application of supercritical fluid chromatography to characterize a labile digitalis-like factor.
Renal Insufficiency
Biochemical abnormalities of platelets in renal failure. Evidence for decreased platelet serotonin, adenosine diphosphate and Mg-dependent adenosine triphosphatase.
Renal Insufficiency
Digoxin in the elderly and in renal failure. Contribution of erythrocyte 86-rubidium uptake tests.
Renal Insufficiency
Digoxin-like immunoreacting substance(s) in the serum of patients with chronic uremia.
Renal Insufficiency
Effects of acute and chronic uremia on active cation transport in rat myocardium.
Renal Insufficiency
Reduction of erythrocyte (Na(+)-K+) ATPase activities in non-insulin-dependent diabetic patients with hyperkalemia.
Renal Insufficiency
Sodium pump isoform specificity for the digitalis-like factor isolated from human peritoneal dialysate.
Renal Insufficiency, Chronic
Ca2+-Mg2+-dependent ATP-ase activity and calcium homeostasis in children with chronic kidney disease.
Renal Insufficiency, Chronic
Decreased ouabain-sensitive adenosine triphosphatase activity in the erythrocyte membrame of patients with chronic renal disease.
Renal Insufficiency, Chronic
Further biochemical characterization of an Na+ pump inhibitor purified from human urine.
Renal Insufficiency, Chronic
Inhibition of Na+,K+-stimulated ATPase in the cochlea of the guinea pig. A potential cause of disturbed inner ear function in terminal renal failure.
Renal Insufficiency, Chronic
[Effect of hemodialysis on erythrocyte acetylcholinesterase and adenosine triphosphatase activity in chronic renal insufficiency]
Reperfusion Injury
Antidigoxin antiserum prevents endogenous digitalis-like compound-mediated reperfusion injury via modulating sodium pump isoform gene expression.
Reperfusion Injury
Modulation of pulmonary NA+ pump gene expression during cold storage and reperfusion.
Reperfusion Injury
[Activity of ectoenzymes of the heart breaking up ATP in the period of myocardial reperfusion after ischemia]
Respiratory Distress Syndrome
Electroporation Mediated Gene Delivery of Na+,K+-ATPase and ENaC Subunits to the Lung Attenuates Acute Respiratory Distress Syndrome in a Two-Hit Porcine Model.
Retinitis Pigmentosa
High mitochondrial DNA T8993G mutation (<90%) without typical features of Leigh's and NARP syndromes.
Rhabdomyolysis
Altered fluid, electrolyte and mineral status in tropical disease, with an emphasis on malaria and leptospirosis.
Rhabdomyolysis
Exertional rhabdomyolysis in a patient with calcium adenosine triphosphatase deficiency.
Rhabdomyosarcoma
Cholinergic stimulation of the Na+/K+ adenosine triphosphatase as revealed by microphysiometry.
Rhabdomyosarcoma, Alveolar
An evaluation of enzyme histochemistry in the diagnosis of childhood rhabdomyosarcoma.
Rheumatoid Nodule
A combined immunohistological and histochemical analysis of lymphocyte and macrophage subpopulations in the rheumatoid nodule.
Rhinitis, Allergic
Inhibition of the sodium, potassium adenosine triphosphatase enzyme in peripheral blood mononuclear cells of subjects with allergic rhinitis.
Rhinitis, Allergic, Seasonal
Quercetin inhibition of the induction and function of cytotoxic T lymphocytes.
Sarcoma
Adenosine triphosphatase activity of crystalline inclusions in alveolar soft part sarcoma. An ultrahistochemical study of a case.
Sarcoma
Essential Oils, Pituranthos chloranthus and Teucrium ramosissimum, Chemosensitize Resistant Human Uterine Sarcoma MES-SA/Dx5 Cells to Doxorubicin by Inducing Apoptosis and Targeting P-Glycoprotein.
Sarcoma
[Effect of dipin on the activity of water soluble adenosine triphosphatase in rats with sarcoma 45]
Sarcoma 180
CYTOCHEMICAL LOCALIZATION OF ADENOSINE TRIPHOSPHATASE IN THE MITOTIC APPARATUS OF HELA AND SARCOMA 180 TISSUE CULTURE CELLS.
Sarcoma 180
Enzymatic responses of transplanted tumour cells towards estrogen, progesterone and testosterone.
Sarcoma, Alveolar Soft Part
Adenosine triphosphatase activity of crystalline inclusions in alveolar soft part sarcoma. An ultrahistochemical study of a case.
Sarcoma, Avian
Increased glucose uptake capacity of Rous-transformed cells and the relevance of deprivation derepression.
Sarcoma, Kaposi
HISTOCHEMISTRY OF KAPOSI'S SARCOMA. II. CHOLINESTERASES, MONOAMINE OXIDASE, AND ADENOSINE TRIPHOSPHATASE.
Sarcoma, Synovial
Cellular differentiation of epithelioid sarcoma. An electron-microscopic, enzyme-histochemical, and immunohistochemical study.
Sarcoma, Yoshida
Increase of adenosine triphosphatase activity of Yoshida sarcoma cells in the process of acquiring resistance to alkylating agents.
Scoliosis
Muscle spindles in the paraspinal musculature of patients with adolescent idiopathic scoliosis.
Seizures
A novel ATP1A2 variant associated with severe stepwise regression, hemiplegia, epilepsy and movement disorders in two unrelated patients.
Seizures
A novel de novo nonsense mutation in ATP1A2 associated with sporadic hemiplegic migraine and epileptic seizures.
Seizures
Assessment of neuropharmacological potential of low molecular weight components extracted from Rhinella schneideri toad poison.
Seizures
Diphenyl diselenide-induced seizures in rat pups: possible interaction with glutamatergic system.
Seizures
Early Treatment in Acute Severe Encephalopathy Caused by ATP1A2 Mutation of Familial Hemiplegic Migraine Type 2: Case Report and Literature Review.
Seizures
Genome-wide screen for modifiers of Na + /K + ATPase alleles identifies critical genetic loci.
Seizures
GM1 ganglioside prevents seizures, Na+,K+-ATPase activity inhibition and oxidative stress induced by glutaric acid and pentylenetetrazole.
Seizures
Increased activity of the sodium-plus-potassium ion-stimulated adenosine triphosphatase in rat brain during electrically induced convulsions.
Seizures
Intrastriatal methylmalonic acid administration induces convulsions and TBARS production, and alters Na+,K+-ATPase activity in the rat striatum and cerebral cortex.
Seizures
Knock-in mouse model of alternating hemiplegia of childhood: behavioral and electrophysiologic characterization.
Seizures
Knockout of sodium pump ?3 subunit gene (Atp1a3(-/-)) results in perinatal seizure and defective respiratory rhythm generation.
Seizures
Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families.
Seizures
Lipoic Acid Alters delta-Aminolevulinic Dehydratase, Glutathione Peroxidase and Na+,K+-ATPase Activities and Glutathione-Reduced Levels in Rat Hippocampus After Pilocarpine-Induced Seizures.
Seizures
Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures.
Seizures
No evidence of ATP1A2 involvement in 12 multiplex Italian families with benign familial infantile seizures.
Seizures
Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions.
Seizures
Reduced ouabain binding to erythrocytes in epilepsy--evidence for a membrane abnormality.
Seizures
Relationship between susceptibility to DMCM-induced generalized motor convulsions and low-affinity [3H]-ouabain binding in membranes in rat brain.
Seizures
Sulfur - Containing Amino Acids Homocysteine And Taurine In Seizures: Current State Of The Art.
Seizures
The effect of vanadate on Na+,K+-ATPase activity of mouse cerebral cortex during bicuculline-induced seizures.
Seizures
Treadmill exercise protects against pentylenetetrazol-induced seizures and oxidative stress after traumatic brain injury.
Seizures, Febrile
Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation.
Sepsis
Glucocorticoid receptor antagonism by mifepristone alters phosphocreatine breakdown during sepsis.
Sepsis
Sepsis increases the plasma membrane content of alpha1 and alpha2 isoforms of Na+-K+ adenosine triphosphatase in rat skeletal muscle.
Sepsis
SERCA1 attenuates diaphragm relaxation and uptake rate of SERCA in rats with acute sepsis.
Severe Acute Respiratory Syndrome
Coronavirus interactions with the cellular autophagy machinery.
Sleep Apnea, Obstructive
2B.03: URIC ACID LEVELS RELATED TO OBSTRUCTIVE SLEEP APNEA SYNDROME IN PATIENTS WITH HYPERTENSION FROM XINJIANG OF CHINA.
Sleep Apnea, Obstructive
Association between uric acid levels and obstructive sleep apnea syndrome in a large epidemiological sample.
Sleep Apnea, Obstructive
Muscle type of palatopharyngeal muscle in children with severe obstructive sleep apnea.
Sleep Deprivation
Na+/K+-ATPase and lipid peroxidation in forebrain cortex and hippocampus of sleep-deprived rats treated with therapeutic lithium concentration for different periods of time.
Sleep Deprivation
Norepinephrine-stimulated increase in Na+, K+-ATPase activity in the rat brain is mediated through alpha1A-adrenoceptor possibly by dephosphorylation of the enzyme.
Spastic Paraplegia, Hereditary
Linking axonal degeneration to microtubule remodeling by Spastin-mediated microtubule severing.
Spastic Paraplegia, Hereditary
Three novel mutations of the spastin gene in Chinese patients with hereditary spastic paraplegia.
Spinal Cord Injuries
Influence of chronic and acute spinal cord injury on skeletal muscle Na+/K+-ATPase and phospholemman expression in humans.
Spinal Cord Injuries
Na+,K+-ATPase concentration and fiber type distribution after spinal cord injury.
Spinal Cord Injuries
The loss-of-function disease-mutation G301R in the Na(+)/K(+)-ATPase ?2 isoform decreases lesion volume and improves functional outcome after acute spinal cord injury in mice.
Squamous Cell Carcinoma of Head and Neck
Expression of copper-transporting P-type adenosine triphosphatase (ATP7B) as a chemoresistance marker in human oral squamous cell carcinoma treated with cisplatin.
Starvation
A chimeric Anabaena/ Escherichia coli KdpD protein (Anacoli KdpD) functionally interacts with E. coli KdpE and activates kdp expression in E. coli.
Starvation
Effects of starvation, feeding, and time of day on the activity of proton transport adenosine triphosphatase in the parietal cells of the mouse gastric glands.
Starvation
Functional analysis of McSnRK1 (SNF1-related protein kinase 1) in regulating Na/K homeostasis in transgenic cultured cells and roots of halophyte Mesembryanthemum crystallinum.
Starvation
Increased glucose uptake capacity of Rous-transformed cells and the relevance of deprivation derepression.
Starvation
Interaction between the autophagy protein Beclin 1 and Na+,K+-ATPase during starvation, exercise, and ischemia.
Starvation
Mg2+ deprivation elicits rapid Ca2+ uptake and activates Ca2+/calcineurin signaling in Saccharomyces cerevisiae.
Starvation
Pma1 is an alkali/alkaline earth metal cation ATPase that preferentially transports Na(+) and K(+) across the Mycobacterium smegmatis plasma membrane.
Starvation
Sodium chloride-induced volume changes of freshwater cyanobacterium Synechococcus sp. PCC 7942 cells can be probed by chlorophyll a fluorescence.
Status Epilepticus
Enzyme histochemistry of the rat hippocampus during experimental status epilepticus.
Status Epilepticus
Long-term decrease in Na+,K+-ATPase activity after pilocarpine-induced status epilepticus is associated with nitration of its alpha subunit.
Status Epilepticus
The role of spreading depression, spreading depolarization and spreading ischemia in neurological disease.
Stomach Neoplasms
Differential sensitivity of human gastric cancer ATPase and normal gastric mucosa ATPase to the synthetic mammalian lignan analogue 2,3-dibenzylbutane-1,4-diol (hattalin).
Stomach Neoplasms
Rabeprazole exhibits antiproliferative effects on human gastric cancer cell lines.
Stomach Neoplasms
The expression of the alpha1 subunit of Na+/K+-ATPase is related to tumor development and clinical outcomes in gastric cancer.
Stomach Ulcer
Potassium bromate cytotoxicity in the Wister rat model of chronic gastric ulcers: Possible reversal by protocatechuic acid.
Stroke
Bone Marrow Mononuclear Cells Transplantation and Training Increased Transplantation of Energy Source Transporters in Chronic Stroke.
Stroke
Marinobufagenin may mediate the impact of salty diets on left ventricular hypertrophy by disrupting the protective function of coronary microvascular endothelium.
Stroke
Polymorphisms in migraine-associated gene, atp1a2, and ischemic stroke risk in a biracial population: the genetics of early onset stroke study.
Tachycardia
[Cancer cell-specific functional relation between Na+,K+-ATPase and volume-regulated anion channel].
Talipes Cavus
The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management.
Tangier Disease
Endoneurial ATPase activity in Tangier disease and other peripheral neuropathies.
Teratocarcinoma
Cloning, expression, and chromosomal mapping of a human ATPase II gene, member of the third subfamily of P-type ATPases and orthologous to the presumed bovine and murine aminophospholipid translocase.
Teratocarcinoma
Ultrastructural localization of membrane phosphatases in teratocarcinoma and early embryos.
Tetanus
Inhibition of vacuolar adenosine triphosphatase antagonizes the effects of clostridial neurotoxins but not phospholipase A2 neurotoxins.
Tetanus
Post-tetanic spontaneous spike activity in rat sympathetic neurons exposed to low potassium ion concentration.
Thyroid Diseases
Erythrocyte sodium/potassium adenosine triphosphatase in thyroid disease and nonthyroidal illness.
Thyroid Diseases
Ion flux and Na+,K+-ATPase activity of erythrocytes and leucocytes in thyroid disease.
Trauma, Nervous System
The Na, K-ATPase alpha3-isoform specifically localizes in the Schmidt-Lanterman incisures of human nerve.
Tremor
Effects of L-phenylalanine on acetylcholinesterase and Na+,K+-ATPase activities in suckling rat frontal cortex, hippocampus and hypothalamus.
Tuberculosis
CtpA, a putative Mycobacterium tuberculosis P-type ATPase, is stimulated by copper (I) in the mycobacterial plasma membrane.
Tuberculosis
CtpB is a plasma membrane copper (I) transporting P-type ATPase of Mycobacterium tuberculosis.
Tuberculosis
Mycobacterium tuberculosis expresses a novel pH-dependent divalent cation transporter belonging to the Nramp family.
Tuberculosis
Pma1 is an alkali/alkaline earth metal cation ATPase that preferentially transports Na(+) and K(+) across the Mycobacterium smegmatis plasma membrane.
Tuberculosis
The P-type ATPase CtpF is a plasma membrane transporter mediating calcium efflux in Mycobacterium tuberculosis cells.
Uremia
An Na, K ATPase inhibitor from ultrafiltrate obtained by hemodialysis of patients with uremia.
Uremia
Effect of chronic renal failure on Na,K-ATPase alpha 1 and alpha 2 mRNA transcription in rat skeletal muscle.
Uremia
Intratympanic steroid injection as a first-line therapy in uremia patients with sudden sensorineural hearing loss.
Urinary Bladder Neck Obstruction
Enhanced force generation by corpus cavernosum smooth muscle in rabbits with partial bladder outlet obstruction.
Urinary Bladder Neoplasms
Bufalin induced apoptosis of bladder carcinoma cells through the inactivation of Na+K+-ATPase.
Uterine Cervical Neoplasms
[Histoenzymatic studies on the behavior of succinic acid dehydrogenase, NADH-2-tetrazolium reductase, adenosine triphosphatase and alkaline phosphatase in cases of uterine cervix cancer]
Vascular System Injuries
Perivascular Delivery of Blebbistatin Reduces Neointimal Hyperplasia Following Carotid Injury in the Mouse.
Ventricular Fibrillation
Digitalis toxicity: lack of marked effect on brain na+,k+-adenosine triphosphatase in the cat.
Vertigo
Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4.
Vibrio Infections
Evidence for disruption of Na(+)-K(+)-ATPase and hsp70 during vibriosis of sea bream, Sparus (=Rhabdosargus) sarba Forsskål.
Virus Diseases
Alterations in monovalent cation transport in Sindbis virus-infected chick cells.
Virus Diseases
Glycolytic control of vacuolar-type ATPase activity: A mechanism to regulate influenza viral infection.
Visna
Adenosine triphosphatase activity during fusion of cultured sheep choroid plexus cells induced by either visna virus or polyethylene glycol.
Whooping Cough
Angiotensin II AT1 receptor/signaling mechanisms in the biphasic effect of the peptide on proximal tubular Na+,K+-ATPase.
Whooping Cough
Colony-stimulating factor 1-induced Na+ influx into human monocytes involves activation of a pertussis toxin-sensitive GTP-binding protein.
Whooping Cough
Salt intake and intestinal dopaminergic activity in adult and old Fischer 344 rats.
Whooping Cough
Seminal fluid factor increases the resistance of the tight junctional complex of cultured human cervical epithelium CaSki cells.
Whooping Cough
The use of the potential-sensitive fluorescent probe bisoxonol in mast cells.
Wolfram Syndrome
Sodium-potassium ATPase 1 subunit is a molecular partner of Wolframin, an endoplasmic reticulum protein involved in ER stress.
Yellow Fever
Strong alkalinization in the anterior midgut of larval yellow fever mosquitoes (Aedes aegypti): involvement of luminal Na+/K+-ATPase.
Zenker Diverticulum
Morphology of the cricopharyngeal muscle in Zenker and control specimens.
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