Disease on EC 2.3.1.43 - phosphatidylcholine-sterol O-acyltransferase
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Abetalipoproteinemia
Molecular species of phosphatidylcholine in abetalipoproteinemia: effect of lecithin:cholesterol acyltransferase and lysolecithin acyltransferase.
Abetalipoproteinemia
Substrate specificity of plasma lecithin: cholesterol acyltransferase in abetalipoproteinemia.
Abetalipoproteinemia
The relationship between serum lipoproteins and red cell membranes in abetalipoproteinemia: deficiency of lecithin:cholesterol acyltransferase.
Abetalipoproteinemia
[Lecithin cholesterol acyltransferase level in 2 cases of abetalipoproteinemia]
Abnormalities, Multiple
Lipoprotein composition in insulin-dependent diabetes mellitus with chronic renal failure: effect of kidney and pancreas transplantation.
adenine phosphoribosyltransferase deficiency
An aid to the diagnosis of genetic disorders underlying adult-onset renal failure: a literature review.
Alagille Syndrome
Cholesterol efflux from Fu5AH cells to the serum of patients with Alagille syndrome. Importance of the hdl-phospholipids/free cholesterol ratio and of the hdl size distribution.
Alagille Syndrome
Glomerular mesangiolipidosis in Alagille syndrome (arteriohepatic dysplasia).
Alagille Syndrome
Lipoprotein pattern and plasma lecithin cholesterol acyl transferase activity in children with Alagille syndrome.
Alzheimer Disease
Characterization and functional studies of lipoproteins, lipid transfer proteins, and lecithin:cholesterol acyltransferase in CSF of normal individuals and patients with Alzheimer's disease.
Amyloidosis
The effects of altered apolipoprotein A-I structure on plasma HDL concentration.
Anemia
Amelioration of circulating lipoprotein profile and proteinuria in a patient with LCAT deficiency due to a novel mutation (Cys74Tyr) in the lid region of LCAT under a fat-restricted diet and ARB treatment.
Anemia
An unusual presentation of LCAT deficiency as nephrotic syndrome with normal serum HDL-C level.
Anemia
Characterization of a new LCAT mutation causing familial LCAT deficiency (FLD) and the role of APOE as a modifier gene of the FLD phenotype.
Anemia
Familial Lecithin:cholesterol acyltransferase deficiency with renal failure in two siblings. First case report from India.
Anemia
Familial lecithin:cholesterol acyltransferase deficiency: First-in-human treatment with enzyme replacement.
Anemia
Lecithin-cholesterol acyltransferase (LCAT) deficiency without mutations in the coding sequence: a case report and literature review.
Anemia
Lecithin:Cholesterol Acyltransferase Activation by Sulfhydryl-Reactive Small Molecules: Role of Cysteine-31.
Anemia
Sex dimorphism in serum lecithin: cholesterol acyltransferase and lipoprotein lipase activities in adult sickle cell anaemia patients with proteinuria.
Anemia
Therapeutic management of a new case of LCAT deficiency with a multifactorial long-term approach based on high doses of angiotensin II receptor blockers (ARBs).
Anemia
[Corneal opacity as the leading symptom of hereditary lecithin-cholesterol acyltransferase (LCAT) deficiency. Case report and a review of the literature]
Anemia, Hemolytic
Corticosteroid treatment of kidney disease in a patient with familial lecithin-cholesterol acyltransferase deficiency.
Anemia, Hemolytic
Novel Missense LCAT Gene Mutation Associated with an Atypical Phenotype of Familial LCAT Deficiency in Two Portuguese Brothers.
Anemia, Hemolytic
Point mutation (C to T) of the LCAT gene resulting in A140C substitution.
Anemia, Hemolytic
Proteinuria in early childhood due to familial LCAT deficiency caused by loss of a disulfide bond in lecithin:cholesterol acyl transferase.
Anemia, Hemolytic
Two novel mutations of lecithin:cholesterol acyltransferase (LCAT) gene and the influence of APOE genotypes on clinical manifestations.
Anemia, Hemolytic
[Characteristics of red cell membrane disorders in the Japanese population]
Anemia, Sickle Cell
Depletion of HDL3 high density lipoprotein and altered functionality of HDL2 in blood from sickle cell patients.
Anemia, Sickle Cell
Sex dimorphism in serum lecithin: cholesterol acyltransferase and lipoprotein lipase activities in adult sickle cell anaemia patients with proteinuria.
Atherosclerosis
Analysis of glomerulosclerosis and atherosclerosis in lecithin cholesterol acyltransferase-deficient mice.
Atherosclerosis
ApoA-II expression in CETP transgenic mice increases VLDL production and impairs VLDL clearance.
Atherosclerosis
Association of lecithin-cholesterol acyltransferase activity and low-density lipoprotein heterogeneity with atherosclerotic cardiovascular disease risk: a longitudinal pilot study.
Atherosclerosis
Atherosclerosis in aged mice over-expressing the reverse cholesterol transport genes.
Atherosclerosis
Carriers of lecithin cholesterol acyltransferase gene mutations have accelerated atherogenesis as assessed by carotid 3.0-T magnetic resonance imaging [corrected].
Atherosclerosis
Cholesteryl ester transfer protein corrects dysfunctional high density lipoproteins and reduces aortic atherosclerosis in lecithin cholesterol acyltransferase transgenic mice.
Atherosclerosis
Controversial Role of Lecithin:Cholesterol Acyltransferase in the Development of Atherosclerosis: New Insights From an LCAT Activator.
Atherosclerosis
Decreased activation of lecithin:cholesterol acyltransferase by glycated apolipoprotein A-I.
Atherosclerosis
Effect of GBOT on blood lipid and blood glucose metabolism in rats with atherosclerosis.
Atherosclerosis
Effects of diazepam (Valium) on aortic atherogenesis and plasma lecithin: cholesterol acyltransferase activity in cockerels fed an atherogenic diet.
Atherosclerosis
Endotoxin-lipoprotein complex formation as a factor in atherogenesis: associations with hyperlipidemia and with lecithin:cholesterol acyltransferase activity.
Atherosclerosis
Evidence that lipid hydroperoxides inhibit plasma lecithin:cholesterol acyltransferase activity.
Atherosclerosis
Hepatic lipase expression in macrophages contributes to atherosclerosis in apoE-deficient and LCAT-transgenic mice.
Atherosclerosis
High-Density Lipoprotein, Lecithin: Cholesterol Acyltransferase, and Atherosclerosis.
Atherosclerosis
Increased plasma HDL cholesterol levels and biliary cholesterol excretion in hamster by LCAT overexpression.
Atherosclerosis
Inhibition of lecithin: cholesterol acyltransferase activity in human blood plasma by cigarette smoke extract and reactive aldehydes.
Atherosclerosis
LCAT cholesterol esterification is associated with the increase of ApoE/ApoA-I ratio during atherosclerosis progression in rabbit.
Atherosclerosis
LCAT modulates atherogenic plasma lipoproteins and the extent of atherosclerosis only in the presence of normal LDL receptors in transgenic rabbits.
Atherosclerosis
Lecithin-cholesterol acryltransferase activity in patients with coronary artery disease examined by coronary angiography.
Atherosclerosis
Lecithin-cholesterol acyltransferase: role in lipoprotein metabolism, reverse cholesterol transport and atherosclerosis.
Atherosclerosis
Lecithin: cholesterol acyltransferase and atherosclerosis: another high-density lipoprotein story that doesn't quite follow the script.
Atherosclerosis
Lecithin: cholesterol acyltransferase--from biochemistry to role in cardiovascular disease.
Atherosclerosis
Lecithin:cholesterol acyltransferase activity in patients with acute myocardial infarction and coronary heart disease.
Atherosclerosis
Lecithin:cholesterol acyltransferase deficiency increases atherosclerosis in the low density lipoprotein receptor and apolipoprotein E knockout mice.
Atherosclerosis
Loss of LCAT Activity in the Golden Syrian Hamster Elicits Pro-atherogenic Dyslipidemia and Enhanced Atherosclerosis.
Atherosclerosis
Marked atherosclerosis in a patient with familiar lecithin: cholesterol acyltransferase deficiency associated with end-stage renal disease and diabetes mellitus.
Atherosclerosis
Methionine sulfoxide reductase A attenuates atherosclerosis via repairing dysfunctional HDL in scavenger receptor class B type I deficient mice.
Atherosclerosis
Mice overexpressing human lecithin: cholesterol acyltransferase are not protected against diet-induced atherosclerosis.
Atherosclerosis
Molecular defect in familial lecithin:cholesterol acyltransferase (LCAT) deficiency: a single nucleotide insertion in LCAT gene causes a complete deficient type of the disease.
Atherosclerosis
Molecular diagnosis of lecithin: cholesterol acyltransferase deficiency in a presymptomatic proband.
Atherosclerosis
Overexpression of human lecithin:cholesterol acyltransferase in mice offers no protection against diet-induced atherosclerosis.
Atherosclerosis
Overexpression of lecithin:cholesterol acyltransferase in transgenic rabbits prevents diet-induced atherosclerosis.
Atherosclerosis
Plasma lecithin: cholesterol acyltransferase activity is elevated in metabolic syndrome and is an independent marker of increased carotid artery intima media thickness.
Atherosclerosis
Plasma low density lipoprotein composition in relation to atherosclerosis in nutritionally defined Vervet monkeys.
Atherosclerosis
Recombinant human Lecithin-Cholesterol acyltransferase in patients with atherosclerosis: Phase 2a primary results and phase 2b design.
Atherosclerosis
Relationship of endogenous hyperleptinemia to serum paraoxonase 1, cholesteryl ester transfer protein, and lecithin cholesterol acyltransferase in obese individuals.
Atherosclerosis
Specificity of lecithin:cholesterol acyltransferase and atherogenic risk: comparative studies on the plasma composition and in vitro synthesis of cholesteryl esters in 14 vertebrate species.
Atherosclerosis
Structure and function of lamellar bodies, lipid-protein complexes involved in storage and secretion of cellular lipids.
Atherosclerosis
Structure and function of lecithin cholesterol acyl transferase: new insights from structural predictions and animal models.
Atherosclerosis
Very low levels of HDL cholesterol and atherosclerosis, a variable relationship--a review of LCAT deficiency.
Atherosclerosis
[Effect of alpha-tocopherol and hyperbaric oxygenation on lipid fatty-acid composition of the plasma in hypercholesteremic rabbits]
Atherosclerosis
[The importance of lecithin-cholesterol acyltransferase (LCAT) in the detection of early forms of atherosclerosis]
Balkan Nephropathy
Partial lecithin:cholesterol acyltransferase (LCAT) deficiency in Balkan endemic nephropathy.
Balkan Nephropathy
The role of lecithin cholesterol acyltransferase and organic substances from coal in the etiology of Balkan endemic nephropathy: A new hypothesis.
Bloom Syndrome
Hereditary lecithin-cholesterol acyltransferase deficiency and Bloom syndrome in the same individual.
Breast Neoplasms
Impaired cholesterol esterification in the plasma in patients with breast cancer.
Breast Neoplasms
Lecithin: cholesterol acyltransferase and na(+)-k(+)-ATPase activity in patients with breast cancer.
Carcinoma, Hepatocellular
Detection of lecithin: cholesterol acyltransferase (LCAT) in a human hepatoma cell line.
Carcinoma, Hepatocellular
Influence of lecithin:cholesterol acyltransferase on cholesterol metabolism in hepatoma cells and hepatocytes.
Carcinoma, Hepatocellular
Plasma lecithin: cholesterol acyltransferase activity in liver disease.
Carcinoma, Hepatocellular
Synthesis and secretion of lecithin-cholesterol acyltransferase by the human hepatoma cell line HepG2.
Cardiovascular Diseases
A simple and precise method to detect sterol esterification activity of lecithin/cholesterol acyltransferase by high-performance liquid chromatography.
Cardiovascular Diseases
Association of lecithin-cholesterol acyltransferase activity and low-density lipoprotein heterogeneity with atherosclerotic cardiovascular disease risk: a longitudinal pilot study.
Cardiovascular Diseases
Genetic lecithin:cholesterol acyltransferase deficiency and cardiovascular disease.
Cardiovascular Diseases
Lecithin: cholesterol acyltransferase activity, HDL-cholesterol and apolipoprotein A in serum of patients undergoing chronic haemodialysis.
Cardiovascular Diseases
Lecithin: cholesterol acyltransferase--from biochemistry to role in cardiovascular disease.
Cardiovascular Diseases
Markedly accelerated catabolism of apolipoprotein A-II (ApoA-II) and high density lipoproteins containing ApoA-II in classic lecithin: cholesterol acyltransferase deficiency and fish-eye disease.
Cardiovascular Diseases
Moderate dietary intake of myristic and alpha-linolenic acids increases lecithin-cholesterol acyltransferase activity in humans.
Cardiovascular Diseases
Premature and severe cardiovascular disease in a Mexican male with markedly low high-density-lipoprotein-cholesterol levels and a mutation in the lecithin:cholesterol acyltransferase gene: A family study.
Carotid Artery Diseases
Low levels of high-density lipoprotein cholesterol due to lecithin:cholesterol acyltransferase mutations increase carotid atherosclerosis.
Cerebral Infarction
[Lecithin-cholesterol acyltransferase gene 608C/T polymorphism associated with atherosclerotic cerebral infarction]
Cholecystolithiasis
A longitudinal analysis of alteration in lecithin-cholesterol acyltransferase and paraoxonase activities following laparoscopic cholecystectomy relative to other parameters of HDL function and the acute phase response.
Cholelithiasis
STUDY OF SERUM AND BILE FROM PATIENTS OF CHOLELITHIASIS IN NORTH-EASTERN INDIA.
Cholestasis
Apolipoprotein and lipid distribution between vesicles and HDL-like particles formed during lipolysis of human very low density lipoproteins by perfused rat heart.
Cholestasis
Depletion of high-density lipoprotein and appearance of triglyceride-rich low-density lipoprotein in a Japanese patient with FIC1 deficiency manifesting benign recurrent intrahepatic cholestasis.
Cholestasis
Effect of heparin on lecithin: cholesterol acyltransferase and lipids in cholestasis.
Cholestasis
Plasma lecithin cholesterol acyl transferase activity, high density lipoprotein cholesterol and cholesterol ester in cholestasis.
Cholestasis
Rapid normalization of severe hypercholesterolemia mediated by lipoprotein X after liver transplantation in a patient with cholestasis - a case report.
Cholestasis
Serum lecithin: cholesterol acyltransferase activity in the bile duct-ligated rat.
Cholestasis
Structure and function of lamellar bodies, lipid-protein complexes involved in storage and secretion of cellular lipids.
Cholestasis
[Cholesterol metabolism and plasma lecithin-cholesterol acyl transferase in experimental hepatitis and cholestasis in the rat]
Cholestasis, Intrahepatic
A critical examination of the value of combined determinations of lecithin:cholesterol acyltransferase and lipoprotein-X in the differential diagnosis of liver disease.
Cholesterol Ester Storage Disease
Cholesteryl ester storage disease with secondary lecithin cholesterol acyl transferase deficiency.
Colorectal Neoplasms
Changes in lecithin: cholesterol acyltransferase, cholesteryl ester transfer protein and paraoxonase-1 activities in patients with colorectal cancer.
Corneal Opacity
Amelioration of circulating lipoprotein profile and proteinuria in a patient with LCAT deficiency due to a novel mutation (Cys74Tyr) in the lid region of LCAT under a fat-restricted diet and ARB treatment.
Corneal Opacity
An unusual presentation of LCAT deficiency as nephrotic syndrome with normal serum HDL-C level.
Corneal Opacity
Characterization of a new LCAT mutation causing familial LCAT deficiency (FLD) and the role of APOE as a modifier gene of the FLD phenotype.
Corneal Opacity
Corneal opacification and lecithin-cholesterol acyltransferase (LCAT) deficiency: a case report.
Corneal Opacity
Corticosteroid treatment of kidney disease in a patient with familial lecithin-cholesterol acyltransferase deficiency.
Corneal Opacity
Familial Lecithin:cholesterol acyltransferase deficiency with renal failure in two siblings. First case report from India.
Corneal Opacity
Familial lecithin:cholesterol acyltransferase deficiency: First-in-human treatment with enzyme replacement.
Corneal Opacity
Lecithin-cholesterol acyltransferase (LCAT) deficiency without mutations in the coding sequence: a case report and literature review.
Corneal Opacity
Molecular defect in familial lecithin:cholesterol acyltransferase (LCAT) deficiency: a single nucleotide insertion in LCAT gene causes a complete deficient type of the disease.
Corneal Opacity
Therapeutic management of a new case of LCAT deficiency with a multifactorial long-term approach based on high doses of angiotensin II receptor blockers (ARBs).
Corneal Opacity
Two novel mutations of lecithin:cholesterol acyltransferase (LCAT) gene and the influence of APOE genotypes on clinical manifestations.
Corneal Opacity
[Corneal opacity as the leading symptom of hereditary lecithin-cholesterol acyltransferase (LCAT) deficiency. Case report and a review of the literature]
Coronary Artery Disease
An unusual presentation of LCAT deficiency as nephrotic syndrome with normal serum HDL-C level.
Coronary Artery Disease
Effect of mild aerobic exercise on serum lipids and apolipoproteins in patients with coronary artery disease.
Coronary Artery Disease
Effect of the cholesterol content of reconstituted LpA-I on lecithin:cholesterol acyltransferase activity.
Coronary Artery Disease
Genetic contributions to quantitative lipoprotein traits associated with coronary artery disease: analysis of a large pedigree from the Bogalusa Heart Study.
Coronary Artery Disease
Glycation of Apoprotein A-I Is Associated With Coronary Artery Plaque Progression in Type 2 Diabetic Patients.
Coronary Artery Disease
Lecithin: cholesterol acyltransferase and lysolecithin in coronary atherosclerosis.
Coronary Artery Disease
Plasma concentrations of LPL and LCAT are in putative association with females and alcohol use which are independent negative risk factors for coronary atherosclerosis among Japanese.
Coronary Artery Disease
Plasma levels of lecithin:cholesterol acyltransferase and risk of future coronary artery disease in apparently healthy men and women - a prospective case-control analysis nested in the EPIC-Norfolk population study.
Coronary Disease
A study of carbohydrate and lipid metabolism in cases of hyperlipidemia and coronary heart disease. II. Preliminary observations on plasma lecithin cholesterol acyl transferase.
Coronary Disease
Beta2-adrenergic activity modulates vascular tone regulation in lecithin:cholesterol acyltransferase knockout mice.
Coronary Disease
High-density lipoprotein metabolism, composition, function, and deficiency.
Coronary Disease
Lecithin:cholesterol acyltransferase activity in patients with acute myocardial infarction and coronary heart disease.
Coronary Disease
MEDI6012: Recombinant Human Lecithin Cholesterol Acyltransferase, High-Density Lipoprotein, and Low-Density Lipoprotein Receptor-Mediated Reverse Cholesterol Transport.
Coronary Disease
Molecular basis for activation of lecithin:cholesterol acyltransferase by a compound that increases HDL cholesterol.
Coronary Disease
Oxidative stress is markedly elevated in lecithin:cholesterol acyltransferase-deficient mice and is paradoxically reversed in the apolipoprotein E knockout background in association with a reduction in atherosclerosis.
Coronary Disease
Safety and Tolerability of ACP-501, a Recombinant Human Lecithin:Cholesterol Acyltransferase, in a Phase 1 Single-Dose Escalation Study.
Cystic Fibrosis
Lipoprotein abnormalities associated with cholesteryl ester transfer activity in cystic fibrosis patients: the role of essential fatty acid deficiency.
Cystinosis
An aid to the diagnosis of genetic disorders underlying adult-onset renal failure: a literature review.
Demyelinating Diseases
A possible mechanism for cholesteryl ester formation during demyelination: lecithin:cholesterol acyltransferase (LCAT) activity in rat brain.
Demyelinating Diseases
Lecithin cholesterol acyltransferase in human cerebrospinal fluid: reduced level in patients with multiple sclerosis and evidence of direct synthesis in the brain.
Diabetes Complications
NO levels in diabetes mellitus: Effects of l-NAME and insulin on LCAT, Na(+)/K(+) ATPase activity and lipid profile.
Diabetes Mellitus
Alterations in high-density lipoprotein metabolism and reverse cholesterol transport in insulin resistance and type 2 diabetes mellitus: role of lipolytic enzymes, lecithin:cholesterol acyltransferase and lipid transfer proteins.
Diabetes Mellitus
Apolipoproteins (A-I, A-II, B), Lp(a) lipoprotein and lecithin: cholesterol acyltransferase activity in diabetes mellitus.
Diabetes Mellitus
Clinofibrate therapy raises high-density lipoprotein levels and lowers atherogenic index in diabetes mellitus patients.
Diabetes Mellitus
Ezetimibe, an inhibitor of Niemann-Pick C1-like 1 protein, decreases cholesteryl ester transfer protein in type 2 diabetes mellitus.
Diabetes Mellitus
Glycaemia and body mass as determinants of plasma lecithin: cholesterol acyltransferase activity in Nigerian patients with non-insulin dependent diabetes mellitus.
Diabetes Mellitus
Lecithin-cholesterol acyltransferase activity in diabetes mellitus and the effect of insulin on these cases.
Diabetes Mellitus
Marked atherosclerosis in a patient with familiar lecithin: cholesterol acyltransferase deficiency associated with end-stage renal disease and diabetes mellitus.
Diabetes Mellitus
NO levels in diabetes mellitus: Effects of l-NAME and insulin on LCAT, Na(+)/K(+) ATPase activity and lipid profile.
Diabetes Mellitus
Oxidized Low-Density Lipoprotein Is Negatively Correlated With Lecithin-Cholesterol Acyltransferase Activity in Type 2 Diabetes Mellitus.
Diabetes Mellitus
Plasma levels of Apolipoprotein A1 and Lecithin:Cholesterol Acyltransferase in type 2 diabetes mellitus: Correlations with haptoglobin phenotypes.
Diabetes Mellitus
Reduced lecithin: cholesterol acyltransferase (LCAT) and Na+, K+, ATPase activity in diabetic patients.
Diabetes Mellitus
Role of lipases, lecithin:cholesterol acyltransferase and cholesteryl ester transfer protein in abnormal high density lipoprotein metabolism in insulin resistance and type 2 diabetes mellitus.
Diabetes Mellitus
[Lecithin-cholesterol acyltransferase (LCAT) activities in diabetes mellitus]
Diabetes Mellitus
[The lipoprotein metabolism in arterial hypertension, type II diabetes mellitus, and metabolic syndrome]
Diabetes Mellitus, Type 1
Fetal macrosomia related to maternal poorly controlled type 1 diabetes strongly impairs serum lipoprotein concentrations and composition.
Diabetes Mellitus, Type 1
Lipoprotein composition in insulin-dependent diabetes mellitus with chronic renal failure: effect of kidney and pancreas transplantation.
Diabetes Mellitus, Type 2
Alterations in high-density lipoprotein metabolism and reverse cholesterol transport in insulin resistance and type 2 diabetes mellitus: role of lipolytic enzymes, lecithin:cholesterol acyltransferase and lipid transfer proteins.
Diabetes Mellitus, Type 2
Ezetimibe, an inhibitor of Niemann-Pick C1-like 1 protein, decreases cholesteryl ester transfer protein in type 2 diabetes mellitus.
Diabetes Mellitus, Type 2
Fasting and postprandial determinants for the occurrence of small dense LDL species in non-insulin-dependent diabetic patients with and without hypertriglyceridaemia: the involvement of insulin, insulin precursor species and insulin resistance.
Diabetes Mellitus, Type 2
Oxidized Low-Density Lipoprotein Is Negatively Correlated With Lecithin-Cholesterol Acyltransferase Activity in Type 2 Diabetes Mellitus.
Diabetes Mellitus, Type 2
Plasma levels of Apolipoprotein A1 and Lecithin:Cholesterol Acyltransferase in type 2 diabetes mellitus: Correlations with haptoglobin phenotypes.
Diabetes Mellitus, Type 2
Plasma lipoprotein composition and cholesteryl ester transfer from high density lipoproteins to very low density and low density lipoproteins in patients with non-insulin-dependent diabetes mellitus.
Diabetes Mellitus, Type 2
Role of lipases, lecithin:cholesterol acyltransferase and cholesteryl ester transfer protein in abnormal high density lipoprotein metabolism in insulin resistance and type 2 diabetes mellitus.
Digestive System Diseases
Lecithin: cholesterol acyltransferase levels in plasma of patients with hepatobiliary disease.
Dirofilariasis
Studies on serum free cholesterol concentration and serum lecithin cholesterol acyltransferase activity in canine dirofilariasis.
Down Syndrome
DYRK1A overexpression decreases plasma lecithin:cholesterol acyltransferase activity and apolipoprotein A-I levels.
Dyslipidemias
Alterations in the fatty acyl composition of plasma cholesteryl esters in Brazilian patients with hepatosplenic schistosomiasis mansoni.
Dyslipidemias
An optimized method for measuring lecithin : cholesterol acyltransferase activity, independent of the concentration and quality of the physiological substrate.
Dyslipidemias
Cholesterol: the good, the bad, and the ugly - therapeutic targets for the treatment of dyslipidemia.
Dyslipidemias
Familial splenomegaly: macrophage hypercatabolism of lipoproteins associated with apolipoprotein E mutation [apolipoprotein E (delta149 Leu)].
Dyslipidemias
Lecithin-cholesterol acyltransferase (LCAT) deficiency without mutations in the coding sequence: a case report and literature review.
Dyslipidemias
Molecular etiology of a dominant form of type III hyperlipoproteinemia caused by R142C substitution in apoE4.
Dyslipidemias
Novel P143L polymorphism of the LCAT gene is associated with dyslipidemia in Chinese patients who have coronary atherosclerotic heart disease.
Dyslipidemias
Splenomegaly with sea-blue histiocytosis, dyslipidemia, and nephropathy in a patient with lecithin-cholesterol acyltransferase deficiency: a clinicopathologic correlation.
Endometrial Neoplasms
Effects of high dose progestin on serum lipids and lipid metabolizing enzymes in patients with endometrial cancer.
Eye Diseases
Alpha-lecithin:cholesterol acyltransferase deficiency. Lack of both phospholipase A2 and acyltransferase activities characteristic of high density lipoprotein lecithin:cholesterol acyltransferase in fish eye disease.
Eye Diseases
Evidence for the presence in human plasma of lecithin: cholesterol acyltransferase activity (beta-LCAT) specifically esterifying free cholesterol of combined pre-beta- and beta-lipoproteins. Studies of fish eye disease patients and control subjects.
Fabry Disease
An aid to the diagnosis of genetic disorders underlying adult-onset renal failure: a literature review.
Fatty Liver
Decreased serum lecithin:cholesterol acyltransferase activity in spontaneous cases of fatty liver in cows.
Fatty Liver
Relevance of apolipoproteins in the development of fatty liver and fatty liver-related peripartum diseases in dairy cows.
Fatty Liver
The activity of lecithin:cholesterol acyltransferase in the serum of cows at parturition or with fatty liver.
Fatty Liver
The association between lecithin-cholesterol acyltransferase activity and fatty liver index.
Fibrosarcoma
Effect of intralipid infusion on serum high- and low-density lipoprotein cholesterol, lecithin:cholesterol acyltransferase, and lipoprotein lipase in tumor-bearing rats.
Friedreich Ataxia
Lecithin: cholesterol acyltransferase activity and fatty acid composition of erythrocyte phospholipids in Friedreich's ataxia.
Genetic Diseases, Inborn
Amelioration of circulating lipoprotein profile and proteinuria in a patient with LCAT deficiency due to a novel mutation (Cys74Tyr) in the lid region of LCAT under a fat-restricted diet and ARB treatment.
Genetic Diseases, Inborn
Arterial hypertension and hyperlipidemia as determinants of glomerulosclerosis.
Genetic Diseases, Inborn
Co-existence of classic familial lecithin-cholesterol acyl transferase deficiency and fish eye disease in the same family.
Genetic Diseases, Inborn
Corticosteroid treatment of kidney disease in a patient with familial lecithin-cholesterol acyltransferase deficiency.
Genetic Diseases, Inborn
LCAT protects against Lipoprotein-X formation in a murine model of drug-induced intrahepatic cholestasis.
Genetic Diseases, Inborn
Lecithin-cholesterol acyltransferase (LCAT) deficiency without mutations in the coding sequence: a case report and literature review.
Genetic Diseases, Inborn
Marked atherosclerosis in a patient with familiar lecithin: cholesterol acyltransferase deficiency associated with end-stage renal disease and diabetes mellitus.
Genetic Diseases, Inborn
Recombinant lecithin:cholesterol acyltransferase containing a Thr123-->Ile mutation esterifies cholesterol in low density lipoprotein but not in high density lipoprotein.
Genetic Diseases, Inborn
The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes.
Genetic Diseases, Inborn
Two different allelic mutations in a Finnish family with lecithin:cholesterol acyltransferase deficiency.
Glomerulonephritis
Effect of polyenoic phospholipid therapy on lecithin cholesterol acyltransferase activity in the human serum.
Glomerulonephritis, Membranoproliferative
Hypocomplementemic type II membranoproliferative glomerulonephritis in a male patient with familial lecithin-cholesterol acyltransferase deficiency due to two different allelic mutations.
glycerol kinase deficiency
Endocrine Dysfunctions in Patients with Inherited Metabolic Diseases.
Graft vs Host Disease
Hypercholesterolemia Due to Lipoprotein X: Case Report and Thematic Review.
Graft vs Host Disease
Rapid normalization of severe hypercholesterolemia mediated by lipoprotein X after liver transplantation in a patient with cholestasis - a case report.
Heart Arrest
Using Literature Based Discovery to Gain Insights Into the Metabolomic Processes of Cardiac Arrest.
Heart Diseases
[Study on the association of lecithin cholesterol acyltransferase gene polymorphisms with the lipid metabolism in coronary atherosclerotic heart disease]
Hepatic Encephalopathy
Serum apoproteins A and B and the lecithin: cholesterol acyl transferase activities in liver cirrhosis and hepatic coma patients.
Hepatitis
Altered lipid composition and differential changes in activities of membrane-bound enzymes of erythrocytes in hepatic cirrhosis.
Hepatitis
D-galactosamine induced hepatitis in the rabbit: effect on lecithin:cholesterol acyltransferase activity, plasma lipid transfer protein activity and high density lipoproteins.
Hepatitis
Serum total lipids, lipoprotein cholesterol, and apolipoprotein A in acute viral hepatitis and chronic liver disease.
Hepatitis
[Cholesterol metabolism and plasma lecithin-cholesterol acyl transferase in experimental hepatitis and cholestasis in the rat]
Hepatitis
[The behavior of lecithin cholesterol acyltransferase (LCAT) in acute viral hepatitis and post-hepatitis cirrhosis]
Hepatitis A
Lipoprotein abnormalities in galactosamine hepatitis: a model of experimental lecithin:cholesterol acyltransferase deficiency.
Hepatitis, Alcoholic
Plasma lipoprotein composition in alcoholic hepatitis: accumulation of apolipoprotein E-rich high density lipoprotein and preferential reappearance of "light'-HDL during partial recovery.
Hepatitis, Alcoholic
The role of lecithin:cholesterol acyltransferase deficiency in the apoprotein metabolism of alcoholic hepatitis.
Hereditary Sensory and Motor Neuropathy
Lipid abnormalities in hereditary neuropathy. Part I. Serum non-polar lipids.
Histiocytosis
Histiocytic and Nonhistiocytic Glomerular Lesions: Foam Cells and Their Mimickers.
Homozygous Familial Hypercholesterolemia
Gene therapy for dyslipidemia: clinical prospects.
Homozygous Familial Hypercholesterolemia
Rapid normalization of severe hypercholesterolemia mediated by lipoprotein X after liver transplantation in a patient with cholestasis - a case report.
Hyaline Membrane Disease
Plasma lecithin-cholesterol acyltransferase deficiency in a child with terminal pulmonary hyaline membrane disease.
Hypercholesterolemia
An unusual presentation of LCAT deficiency as nephrotic syndrome with normal serum HDL-C level.
Hypercholesterolemia
Effect of hypercholesteremia on the activity of serum lecithin-cholesterol acyltransferase.
Hypercholesterolemia
Effects of HMG-CoA reductase inhibition on hepatic expression of key cholesterol-regulatory enzymes and receptors in nephrotic syndrome.
Hypercholesterolemia
Effects of probucol and pravastatin on plasma lipids, activities of postheparin lipoprotein lipase, and lecithin cholesterol acyltransferase and apo A-I containing lipoproteins with and without apo A-II in patients with moderate hypercholesterolemia.
Hypercholesterolemia
Effects of vitamin E and HMG-CoA reductase inhibition on cholesteryl ester transfer protein and lecithin-cholesterol acyltransferase in hypercholesterolemia.
Hypercholesterolemia
New model of atherosclerosis in insulin resistant sand rats: hypercholesterolemia combined with D2 vitamin.
Hypercholesterolemia
Prebeta-migrating high density lipoprotein: quantitation in normal and hyperlipidemic plasma by solid phase radioimmunoassay following electrophoretic transfer.
Hypercholesterolemia
Rapid normalization of severe hypercholesterolemia mediated by lipoprotein X after liver transplantation in a patient with cholestasis - a case report.
Hypercholesterolemia
Serum activity and hepatic secretion of lecithin:cholesterol acyltransferase in experimental hypothyroidism and hypercholesterolemia.
Hyperhomocysteinemia
Corrective effects of hepatotoxicity by hepatic Dyrk1a gene delivery in mice with intermediate hyperhomocysteinemia.
Hyperinsulinism
Influence of insulin sensitivity and the TaqIB cholesteryl ester transfer protein gene polymorphism on plasma lecithin:cholesterol acyltransferase and lipid transfer protein activities and their response to hyperinsulinemia in non-diabetic men.
Hyperinsulinism
New model of atherosclerosis in insulin resistant sand rats: hypercholesterolemia combined with D2 vitamin.
Hyperlipidemia, Familial Combined
Evidence against alterations in Lecithin:cholesterol acyltransferase (LCAT) activity in familial combined hyperlipidemia.
Hyperlipidemia, Familial Combined
Linkage of a candidate gene locus to familial combined hyperlipidemia: lecithin:cholesterol acyltransferase on 16q.
Hyperlipidemias
A novel homozygous mutation causing lecithin-cholesterol acyltransferase deficiency in a proband of Romanian origin with a record of extreme gestational hyperlipidemia.
Hyperlipidemias
A study of carbohydrate and lipid metabolism in cases of hyperlipidemia and coronary heart disease. II. Preliminary observations on plasma lecithin cholesterol acyl transferase.
Hyperlipidemias
Acyl-coenzyme A:cholesterol acyltransferase inhibition ameliorates proteinuria, hyperlipidemia, lecithin-cholesterol acyltransferase, SRB-1, and low-denisty lipoprotein receptor deficiencies in nephrotic syndrome.
Hyperlipidemias
Characteristic, polymorphism and expression distribution of LCAT gene in a Mongolian gerbil model for hyperlipidemia.
Hyperlipidemias
Cholesteryl ester flux from HDL to VLDL-1 is preferentially enhanced in type IIB hyperlipidemia in the postprandial state.
Hyperlipidemias
Effect of simian virus 40 subcutaneous tumors on circulating lipids and lipoproteins in the Syrian hamster.
Hyperlipidemias
Effects of oral selenium and magnesium co-supplementation on lipid metabolism, antioxidative status, histopathological lesions, and related gene expression in rats fed a high-fat diet.
Hyperlipidemias
Endotoxin-lipoprotein complex formation as a factor in atherogenesis: associations with hyperlipidemia and with lecithin:cholesterol acyltransferase activity.
Hyperlipidemias
Evidence against alterations in Lecithin:cholesterol acyltransferase (LCAT) activity in familial combined hyperlipidemia.
Hyperlipidemias
High density lipoproteins with differing apolipoproteins: relationships to postprandial lipemia, cholesteryl ester transfer protein, and activities of lipoprotein lipase, hepatic lipase, and lecithin: cholesterol acyltransferase.
Hyperlipidemias
Linkage of a candidate gene locus to familial combined hyperlipidemia: lecithin:cholesterol acyltransferase on 16q.
Hyperlipidemias
Metabolism of lysolecithin in vivo: effects of hyperlipemia and atherosclerosis in squirrel monkeys.
Hyperlipidemias
Regulation of plasma lecithin:cholesterol acyltransferase in man. III. Role of high density lipoprotein cholesteryl esters in the activating effect of a high-fat test meal.
Hyperlipidemias
Regulation of plasma lecithin:cholesterol acyltransferase. II. Activation during alimentary lipemia.
Hyperlipidemias
The lipemia in familial plasma lecithin: cholesterol acyltransferase deficiency.
Hyperlipidemias
Thrombin binding and response in platelets from patients with dyslipoproteinemias: increased stimulus-response coupling in type II hyperlipoproteinemia.
Hyperlipidemias
[Effect of Astragalus Angelica Mixture on lipoprotein lipase and lecithin cholesterol acyltransferase of nephrotic rats]
Hyperlipoproteinemia Type I
Concentrations of electrophoretic and size subclasses of apolipoprotein A-I-containing particles in human peripheral lymph.
Hyperlipoproteinemia Type II
Decrease of plasma large, light LDL (LDL1), HDL2 and HDL3 levels with concomitant increase of cholesteryl ester transfer protein (CETP) activity by probucol in type II hyperlipoproteinemia.
Hyperlipoproteinemia Type II
Effects of pravastatin on lipid transfer protein and lecithin cholesterol acyltransferase in heterozygous familial hypercholesterolemia.
Hyperlipoproteinemia Type II
Lecithin: cholesterol acyltransferase activity in familial hypercholesterolemia treated with simvastatin and simvastatin plus low-dose colestipol.
Hyperlipoproteinemia Type II
Low-dose colestipol plus fenofibrate: effects on plasma lipoproteins, lecithin:cholesterol acyltransferase, and postheparin lipases in familial hypercholesterolemia.
Hyperlipoproteinemia Type III
Characterization of guinea pig plasma lipoproteins: the appearance of new lipoproteins in response to dietary cholesterol.
Hyperlipoproteinemias
Abnormal lipoprotein and apolipoprotein pattern in lipoprotein glomerulopathy.
Hyperlipoproteinemias
Characterization of guinea pig plasma lipoproteins: the appearance of new lipoproteins in response to dietary cholesterol.
Hyperlipoproteinemias
Decrease of plasma large, light LDL (LDL1), HDL2 and HDL3 levels with concomitant increase of cholesteryl ester transfer protein (CETP) activity by probucol in type II hyperlipoproteinemia.
Hyperlipoproteinemias
Determination of apolipoprotein A and its constitutive A-I and A-II polypeptides by separate electroimmunoassays.
Hyperlipoproteinemias
Effects of bezafibrate therapy on subfractions of plasma low-density lipoprotein and high-density lipoprotein, and on activities of lecithin:cholesterol acyltransferase and cholesteryl ester transfer protein in patients with hyperlipoproteinemia.
Hyperlipoproteinemias
Hyperlipoproteinemia in Nagase analbuminemic rats: effects of pravastatin on plasma (apo)lipoproteins and lecithin:cholesterol acyltransferase activity.
Hyperlipoproteinemias
Lecithin:cholesterol acyltransferase as a possible diagnostic tool in ischemic heart disease.
Hyperlipoproteinemias
Regulation of plasma lecithin:cholesterol acyltransferase in man. I. Increased activity in primary hypertriglyceridemia.
Hyperlipoproteinemias
Similar behaviour of lecithin:cholesterol acyltransferase and pseudocholinesterase in liver disease and hyperlipoproteinemia.
Hyperlipoproteinemias
[Relationship between the activity of lecithin cholesterol acyltransferase, hyperlipoproteinemia type and the indicators of the system of hemostasis in chronic ischemic heart disease]
Hyperoxaluria, Primary
An aid to the diagnosis of genetic disorders underlying adult-onset renal failure: a literature review.
Hypertension
Lecithin:cholesterol acyltransferase as a possible diagnostic tool in ischemic heart disease.
Hypertension
Serum lecithin: cholesterol acyltransferase activity, HDL2 and HDL3 composition in hypertensive mothers and their small for gestational age newborns.
Hypertension
[Basal lecithin:cholesterol acyltransferase activity in patients with hypertension (author's transl)]
Hypertension
[The lipoprotein metabolism in arterial hypertension, type II diabetes mellitus, and metabolic syndrome]
Hypertension, Pregnancy-Induced
Serum lecithin: cholesterol acyltransferase activity, HDL2 and HDL3 composition in hypertensive mothers and their small for gestational age newborns.
Hyperthyroidism
Lecithin: cholesterol acyl transfer rate in hypothyroidism and hyperthyroidism.
Hyperthyroidism
Plasma lecithin: cholesterol acyltransferase activity in hypo- and hyperthyroidism.
Hypertriglyceridemia
ApoA-II expression in CETP transgenic mice increases VLDL production and impairs VLDL clearance.
Hypertriglyceridemia
Charge-based heterogeneity of human plasma lipoproteins at hypertriglyceridemia: capillary isotachophoresis study.
Hypertriglyceridemia
Clinical presentation, laboratory values, and coronary heart disease risk in marked high-density lipoprotein-deficiency states.
Hypertriglyceridemia
Clinical, biochemical, and genetic features in familial disorders of high density lipoprotein deficiency.
Hypertriglyceridemia
Coordinated alteration of hepatic gene expression in fatty acid and triglyceride synthesis in LCAT-null mice is associated with altered PUFA metabolism.
Hypertriglyceridemia
Familial splenomegaly: macrophage hypercatabolism of lipoproteins associated with apolipoprotein E mutation [apolipoprotein E (delta149 Leu)].
Hypertriglyceridemia
Hypertriglyceridemia in lecithin-cholesterol acyltransferase-deficient mice is associated with hepatic overproduction of triglycerides, increased lipogenesis, and improved glucose tolerance.
Hypertriglyceridemia
Lecithin-cholesterol acyltransferase activity in carbohydrate-induced hypertriglyceridemia in mice.
Hypertriglyceridemia
Prebeta-migrating high density lipoprotein: quantitation in normal and hyperlipidemic plasma by solid phase radioimmunoassay following electrophoretic transfer.
Hypertriglyceridemia
Regulation of plasma lecithin:cholesterol acyltransferase in man. I. Increased activity in primary hypertriglyceridemia.
Hypertriglyceridemia
Similar behaviour of lecithin:cholesterol acyltransferase and pseudocholinesterase in liver disease and hyperlipoproteinemia.
Hypoalbuminemia
Acyl-coenzyme A:cholesterol acyltransferase inhibition ameliorates proteinuria, hyperlipidemia, lecithin-cholesterol acyltransferase, SRB-1, and low-denisty lipoprotein receptor deficiencies in nephrotic syndrome.
Hypoalphalipoproteinemias
Analysis of apolipoprotein A-I, lecithin:cholesterol acyltransferase and glucocerebrosidase genes in hypoalphalipoproteinemia.
Hypoalphalipoproteinemias
Beta2-adrenergic activity modulates vascular tone regulation in lecithin:cholesterol acyltransferase knockout mice.
Hypoalphalipoproteinemias
Clinical variant of Tangier disease in Japan: mutation of the ABCA1 gene in hypoalphalipoproteinemia with corneal lipidosis.
Hypoalphalipoproteinemias
Correction of hypoalphalipoproteinemia in LDL receptor-deficient rabbits by lecithin:cholesterol acyltransferase.
Hypoalphalipoproteinemias
Functional Lecithin: Cholesterol Acyltransferase Is Not Required for Efficient Atheroprotection in Humans.
Hypoalphalipoproteinemias
Functional lecithin: cholesterol acyltransferase is not required for efficient atheroprotection in humans.
Hypoalphalipoproteinemias
Identification and functional analysis of missense mutations in the lecithin cholesterol acyltransferase gene in a Chilean patient with hypoalphalipoproteinemia.
Hypoalphalipoproteinemias
Molecular genetic study of Finns with hypoalphalipoproteinemia and hyperalphalipoproteinemia: a novel Gly230 Arg mutation (LCAT[Fin]) of lecithin:cholesterol acyltransferase (LCAT) accounts for 5% of cases with very low serum HDL cholesterol levels.
Hypoalphalipoproteinemias
Oxidative stress is markedly elevated in lecithin:cholesterol acyltransferase-deficient mice and is paradoxically reversed in the apolipoprotein E knockout background in association with a reduction in atherosclerosis.
Hypoalphalipoproteinemias
[Familial alpha lipoprotein deficiency. Tangier disease, familial hypoalphalipoproteinemia and familial deficiency of lecithin cholesterol acyltransferase deficiency]
Hypobetalipoproteinemias
Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin:cholesterol acyltransferase deficiency and hypobetalipoproteinemia.
Hypothyroidism
A case of congenital nephrotic syndrome associated with partial deficiency of lecithin cholesterol acyltransferase (LCAT) and hypothyroidism.
Hypothyroidism
Serum activity and hepatic secretion of lecithin:cholesterol acyltransferase in experimental hypothyroidism and hypercholesterolemia.
Infections
A Lipolytic Lecithin:Cholesterol Acyltransferase Secreted by Toxoplasma Facilitates Parasite Replication and Egress.
Insulin Resistance
Alterations in high-density lipoprotein metabolism and reverse cholesterol transport in insulin resistance and type 2 diabetes mellitus: role of lipolytic enzymes, lecithin:cholesterol acyltransferase and lipid transfer proteins.
Insulin Resistance
Fasting and postprandial determinants for the occurrence of small dense LDL species in non-insulin-dependent diabetic patients with and without hypertriglyceridaemia: the involvement of insulin, insulin precursor species and insulin resistance.
Insulin Resistance
Influence of insulin sensitivity and the TaqIB cholesteryl ester transfer protein gene polymorphism on plasma lecithin:cholesterol acyltransferase and lipid transfer protein activities and their response to hyperinsulinemia in non-diabetic men.
Insulin Resistance
Lecithin cholesterol acyltransferase (LCAT) null mice are protected from diet-induced obesity and insulin resistance in a gender specific manner through multiple pathways.
Insulin Resistance
Lecithin cholesterol acyltransferase deficiency protects from diet-induced insulin resistance and obesity--novel insights from mouse models.
Insulin Resistance
Lecithin:cholesterol acyltransferase deficiency protects against cholesterol-induced hepatic endoplasmic reticulum stress in mice.
Insulin Resistance
Role of lipases, lecithin:cholesterol acyltransferase and cholesteryl ester transfer protein in abnormal high density lipoprotein metabolism in insulin resistance and type 2 diabetes mellitus.
Kearns-Sayre Syndrome
Endocrine Dysfunctions in Patients with Inherited Metabolic Diseases.
Ketosis
Decreased concentration of serum apolipoprotein C-III in cows with fatty liver, ketosis, left displacement of the abomasum, milk fever and retained placenta.
Ketosis
Lecithin cholesterol acyltransferase (LCAT) activity as a predictor for ketosis and parturient haemoglobinuria in Egyptian water buffaloes.
Ketosis
Reduced activity of lecithin:cholesterol acyltransferase in the serum of cows with ketosis and left displacement of the abomasum.
Ketosis
Reduction in serum lecithin:cholesterol acyltransferase activity prior to the occurrence of ketosis and milk fever in cows.
Kidney Diseases
Corticosteroid treatment of kidney disease in a patient with familial lecithin-cholesterol acyltransferase deficiency.
Kidney Failure, Chronic
Changes in lipoprotein profile and urinary albumin excretion in familial LCAT deficiency with lipid lowering therapy.
Kidney Failure, Chronic
Changes in plasma lecithin: cholesterol acyltransferase activity, HDL(2), HDL(3) amounts and compositions in patients with chronic renal failure after different times of hemodialysis.
Kidney Failure, Chronic
Down-regulation of hepatic lecithin:cholesterol acyltransferase gene expression in chronic renal failure.
Kidney Failure, Chronic
Effect of long-term hemodialysis on plasma lecithin: cholesterol acyltransferase activity and the amounts and compositions of HDL2 and HDL3 in hemodialysis-treated patients with chronic renal failure: a 9-year longitudinal study.
Kidney Failure, Chronic
Effect of recombinant human lecithin cholesterol acyltransferase infusion on lipoprotein metabolism in mice.
Kidney Failure, Chronic
Effect of treatment with simvastatin on serum cholesteryl ester transfer in patients on dialysis. PERFECT Study Collaborative Group.
Kidney Failure, Chronic
Familial Lecithin:cholesterol acyltransferase deficiency with renal failure in two siblings. First case report from India.
Kidney Failure, Chronic
Lecithin-cholesterol acyltransferase (LCAT) deficiency without mutations in the coding sequence: a case report and literature review.
Kidney Failure, Chronic
Marked atherosclerosis in a patient with familiar lecithin: cholesterol acyltransferase deficiency associated with end-stage renal disease and diabetes mellitus.
Kidney Failure, Chronic
Plasma phospholipid transfer protein, cholesteryl ester transfer protein and lecithin:cholesterol acyltransferase in end-stage renal disease (ESRD).
Kidney Failure, Chronic
Sequential kidney-liver transplantation from the same living donor for lecithin cholesterol acyl transferase (LCAT) deficiency.
Kidney Failure, Chronic
Therapeutic management of a new case of LCAT deficiency with a multifactorial long-term approach based on high doses of angiotensin II receptor blockers (ARBs).
Kwashiorkor
Plasma lecithin-cholesterol acyltransferase activity and plasma lipoprotein composition and concentrations in kwashiorkor.
Lecithin Cholesterol Acyltransferase Deficiency
A case of acquired lecithin:cholesterol acyltransferase deficiency with sarcoidosis that remitted spontaneously.
Lecithin Cholesterol Acyltransferase Deficiency
A molecular defect causing fish eye disease: an amino acid exchange in lecithin-cholesterol acyltransferase (LCAT) leads to the selective loss of alpha-LCAT activity.
Lecithin Cholesterol Acyltransferase Deficiency
A new molecular defect in the lecithin: cholesterol acyltransferase (LCAT) gene associated with fish eye disease.
Lecithin Cholesterol Acyltransferase Deficiency
A novel frameshift mutation of the lecithin:cholesterol acyltransferase (LCAT) gene associated with renal failure in familial LCAT deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
A novel missense mutation (Asn5-->Ile) in lecithin: cholesterol acyltransferase (LCAT) gene in a Japanese patient with LCAT deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
A proteomic approach to identify novel disease biomarkers in LCAT deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
A review on lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
A study of the small spherical high density lipoproteins of patients afflicted with familial lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
A study of the structure of the gene for lecithin: cholesterol acyltransferase in four unrelated individuals with familial lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Abnormal lipoprotein appearing in plasma of patients who received a ten percent soybean oil emulsion infusion.
Lecithin Cholesterol Acyltransferase Deficiency
Abnormalities in lipoproteins of d < 1.006 g/ml in familial lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Abnormalities in plasma lipoprotein in familial partial lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Acquired lecithin:cholesterol acyltransferase deficiency as a major factor in lowering plasma HDL levels in chronic kidney disease.
Lecithin Cholesterol Acyltransferase Deficiency
Activation of lipoprotein lipase by lipoprotein fractions of human serum.
Lecithin Cholesterol Acyltransferase Deficiency
Alpha-lecithin:cholesterol acyltransferase deficiency. Lack of both phospholipase A2 and acyltransferase activities characteristic of high density lipoprotein lecithin:cholesterol acyltransferase in fish eye disease.
Lecithin Cholesterol Acyltransferase Deficiency
Amino acid composition of serum high density lipoprotein in patients with familial lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
An amino acid exchange in exon I of the human lecithin: cholesterol acyltransferase (LCAT) gene is associated with fish eye disease.
Lecithin Cholesterol Acyltransferase Deficiency
An intronic mutation in a lariat branchpoint sequence is a direct cause of an inherited human disorder (fish-eye disease).
Lecithin Cholesterol Acyltransferase Deficiency
Analysis of familial hypoalphalipoproteinemia syndromes.
Lecithin Cholesterol Acyltransferase Deficiency
ApoA-II expression in CETP transgenic mice increases VLDL production and impairs VLDL clearance.
Lecithin Cholesterol Acyltransferase Deficiency
Apolipoprotein AIMilano. Partial lecithin:cholesterol acyltransferase deficiency due to low levels of a functional enzyme.
Lecithin Cholesterol Acyltransferase Deficiency
Apolipoprotein and lipid distribution between vesicles and HDL-like particles formed during lipolysis of human very low density lipoproteins by perfused rat heart.
Lecithin Cholesterol Acyltransferase Deficiency
Apolipoproteins and lipoprotein families in familial lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Cardiac surgery for a patient with familial lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Case Report: Management of Corneal Clouding from Lecithin: Cholesterol Acyltransferase Deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Catalytically inactive lecithin: cholesterol acyltransferase (LCAT) caused by a Gly 30 to Ser mutation in a family with LCAT deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Changes in lipoprotein profile and urinary albumin excretion in familial LCAT deficiency with lipid lowering therapy.
Lecithin Cholesterol Acyltransferase Deficiency
Characterization of a new LCAT mutation causing familial LCAT deficiency (FLD) and the role of APOE as a modifier gene of the FLD phenotype.
Lecithin Cholesterol Acyltransferase Deficiency
Characterization of apolipoprotein E-rich high density lipoproteins in familial lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Characterization of guinea pig plasma lipoproteins: the appearance of new lipoproteins in response to dietary cholesterol.
Lecithin Cholesterol Acyltransferase Deficiency
Characterization of subspecies of apolipoprotein A-I-containing lipoprotein in homozygotes for familial lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Characterization of subspecies of lipoprotein containing apolipoprotein A-I in heterozygotes for familial lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Characterization of the effects of mutations in the putative branchpoint sequence of intron 4 on the splicing within the human lecithin:cholesterol acyltransferase gene.
Lecithin Cholesterol Acyltransferase Deficiency
Classical LCAT deficiency resulting from a novel homozygous dinucleotide deletion in exon 4 of the human lecithin: cholesterol acyltransferase gene causing a frameshift and stop codon at residue 144.
Lecithin Cholesterol Acyltransferase Deficiency
Co-existence of classic familial lecithin-cholesterol acyl transferase deficiency and fish eye disease in the same family.
Lecithin Cholesterol Acyltransferase Deficiency
Combined liver-kidney transplantation for rare diseases.
Lecithin Cholesterol Acyltransferase Deficiency
Compound heterozygosity (G71R/R140H) in the lecithin:cholesterol acyltransferase (LCAT) gene results in an intermediate phenotype between LCAT-deficiency and fish-eye disease.
Lecithin Cholesterol Acyltransferase Deficiency
Concentrations of electrophoretic and size subclasses of apolipoprotein A-I-containing particles in human peripheral lymph.
Lecithin Cholesterol Acyltransferase Deficiency
Corneal changes in the dislipoproteinaemias.
Lecithin Cholesterol Acyltransferase Deficiency
Decreased sodium influx and abnormal red cell membrane lipids in a patient with familial plasma lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Demonstration of intact intracellular cholesterol esterification and normal low-density lipoprotein pathway in fibroblasts from a patient with lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Detection of erythrocyte membrane structural abnormalities in lecithin: cholesterol acyltransferase deficiency using a spin label approach.
Lecithin Cholesterol Acyltransferase Deficiency
Determination of apolipoprotein A and its constitutive A-I and A-II polypeptides by separate electroimmunoassays.
Lecithin Cholesterol Acyltransferase Deficiency
Different substrate specificities of plasma lecithin: cholesterol acyl transferase in fish eye disease and Tangier disease.
Lecithin Cholesterol Acyltransferase Deficiency
Differential diagnosis of Schnyder corneal dystrophy.
Lecithin Cholesterol Acyltransferase Deficiency
Differential phenotypic expression by three mutant alleles in familial lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Disturbed apolipoprotein A-I-containing lipoproteins in fish-eye disease are improved by the lecithin:cholesterol acyltransferase produced by gene-transduced adipocytes in vitro.
Lecithin Cholesterol Acyltransferase Deficiency
Effect of early enteral feeding on apolipoprotein AI levels and high-density lipoprotein heterogeneity in preterm infants.
Lecithin Cholesterol Acyltransferase Deficiency
Effects of long-term, low-fat diet on plasma apo E in familial LCAT deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Effects of plasma infusion on plasma lipids, apoproteins and plasma enzyme activities in familial lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Enzymic esterification of cholesterol in rat intestinal mucosa catalyzed by acyl-CoA: cholesterol acyltransferase.
Lecithin Cholesterol Acyltransferase Deficiency
Erythrocyte alterations in praseodymium-induced lecithin:cholesterol acyltransferase (LCAT) deficiency in the rat: comparison with familial LCAT deficiency in man.
Lecithin Cholesterol Acyltransferase Deficiency
Erythrocyte membrane alterations in lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Evidence for deficiency of high density lipoprotein lecithin: cholesterol acyltransferase activity (alpha-LCAT) in fish eye disease.
Lecithin Cholesterol Acyltransferase Deficiency
Evidence for impaired cellular cholesterol removal mediated by apo A-I containing lipoproteins in patients with familial lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Evidence for the presence in human plasma of lecithin: cholesterol acyltransferase activity (beta-LCAT) specifically esterifying free cholesterol of combined pre-beta- and beta-lipoproteins. Studies of fish eye disease patients and control subjects.
Lecithin Cholesterol Acyltransferase Deficiency
Familial LCAT deficiency and fish-eye disease.
Lecithin Cholesterol Acyltransferase Deficiency
Familial lecithin-cholesterol acyltransferase deficiency in a Japanese family: evidence for functionally defective enzyme in homozygotes and obligate heterozygotes.
Lecithin Cholesterol Acyltransferase Deficiency
Familial lecithin-cholesterol acyltransferase: identification of heterozygotes with half-normal enzyme activity and mass.
Lecithin Cholesterol Acyltransferase Deficiency
Familial lecithin: cholesterol acyltransferase deficiency complicated with unconjugated hyperbilirubinemia and peripheral neuropathy. The first reported cases in the Far East.
Lecithin Cholesterol Acyltransferase Deficiency
Familial lecithin: cholesterol acyltransferase deficiency. Study of two new patients and their close relatives.
Lecithin Cholesterol Acyltransferase Deficiency
Familial lecithin:cholesterol acyltransferase deficiency - a new metabolic disease with renal involvement.
Lecithin Cholesterol Acyltransferase Deficiency
Familial Lecithin:cholesterol acyltransferase deficiency with renal failure in two siblings. First case report from India.
Lecithin Cholesterol Acyltransferase Deficiency
Familial lecithin:cholesterol acyltransferase deficiency. Biochemistry of the cornea.
Lecithin Cholesterol Acyltransferase Deficiency
Familial lecithin:cholesterol acyltransferase deficiency. Further studies on plasma lipoproteins and plasma postheparin lipase activity of a patient with normal renal function.
Lecithin Cholesterol Acyltransferase Deficiency
Familial lecithin:cholesterol acyltransferase deficiency. Report of a fourth family from northwestern Norway.
Lecithin Cholesterol Acyltransferase Deficiency
Familial lecithin:cholesterol acyltransferase deficiency. Report of a third Norwegian family with two afflicted members.
Lecithin Cholesterol Acyltransferase Deficiency
Familial lecithin:cholesterol acyltransferase deficiency. Studies on lipid composition and morphology of tissues.
Lecithin Cholesterol Acyltransferase Deficiency
Familial lecithin:cholesterol acyltransferase deficiency. Ultrastructural studies on lipid deposition and tissue reactions.
Lecithin Cholesterol Acyltransferase Deficiency
Familial lecithin:cholesterol acyltransferase deficiency: First-in-human treatment with enzyme replacement.
Lecithin Cholesterol Acyltransferase Deficiency
Familial lecithin:cholesterol acyltransferase deficiency: further resolution of lipoprotein particle heterogeneity in the low density interval.
Lecithin Cholesterol Acyltransferase Deficiency
Familial lecithin:cholesterol acyltransferase deficiency: molecular analysis of a compound heterozygote: LCAT (Arg147 --> Trp) and LCAT (Tyr171 --> Stop).
Lecithin Cholesterol Acyltransferase Deficiency
Familial plasma lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Familial plasma lecithin: cholesterol acyltransferase deficiency. A new family with partial LCAT activity.
Lecithin Cholesterol Acyltransferase Deficiency
Familial plasma lecithin: cholesterol acyltransferase deficiency. A study of the platelets.
Lecithin Cholesterol Acyltransferase Deficiency
Familial splenomegaly: macrophage hypercatabolism of lipoproteins associated with apolipoprotein E mutation [apolipoprotein E (delta149 Leu)].
Lecithin Cholesterol Acyltransferase Deficiency
Finding a very rare mutation in non-Caucasian LCAT patients from Southwest Asia for the first time.
Lecithin Cholesterol Acyltransferase Deficiency
Free cholesterol deposition in the cornea of human apolipoprotein A-II transgenic mice with functional lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Functional Lecithin: Cholesterol Acyltransferase Is Not Required for Efficient Atheroprotection in Humans.
Lecithin Cholesterol Acyltransferase Deficiency
Functional lecithin: cholesterol acyltransferase is not required for efficient atheroprotection in humans.
Lecithin Cholesterol Acyltransferase Deficiency
Functional lecithin:cholesterol acyltransferase deficiency and high density lipoprotein deficiency in transgenic mice overexpressing human apolipoprotein A-II.
Lecithin Cholesterol Acyltransferase Deficiency
Genetic control of lecithin-cholesterol acyltransferase (LCAT): measurement of LCAT mass in a large kindred with LCAT deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Genetic lecithin:cholesterol acyltransferase deficiency and cardiovascular disease.
Lecithin Cholesterol Acyltransferase Deficiency
Hereditary lecithin cholesterol acyltransferase deficiency. Report of a new family with two afflicted sisters.
Lecithin Cholesterol Acyltransferase Deficiency
Hereditary lecithin-cholesterol acyltransferase deficiency and Bloom syndrome in the same individual.
Lecithin Cholesterol Acyltransferase Deficiency
Heterogeneity of nascent high density lipoproteins secreted by the hepatoma-derived cell line, Hep G2.
Lecithin Cholesterol Acyltransferase Deficiency
Human lecithin:cholesterol acyltransferase deficiency: in vivo kinetics of low-density lipoprotein and lipoprotein-X.
Lecithin Cholesterol Acyltransferase Deficiency
Hypoalphalipoproteinemia resembling fish eye disease.
Lecithin Cholesterol Acyltransferase Deficiency
Identification of lipoprotein families in familial lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Identification of the abnormal cholestatic lipoprotein (LP-X) in familial lecithin:Cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
In vitro effects of lecithin:cholesterol acyltransferase on apolipoprotein distribution in familial lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
In vitro expression of natural mutants of human lecithin:cholesterol acyltransferase.
Lecithin Cholesterol Acyltransferase Deficiency
In vitro expression of structural defects in the lecithin-cholesterol acyltransferase gene.
Lecithin Cholesterol Acyltransferase Deficiency
In vitro normalization of cholesteryl ester content and particle size of fish eye disease high density lipoproteins.
Lecithin Cholesterol Acyltransferase Deficiency
Inhibitory effect of normal high density lipoproteins on lecithin:cholesterol acyltransferase activity in fish eye disease plasma.
Lecithin Cholesterol Acyltransferase Deficiency
Isolated low HDL-cholesterol as an important risk factor for coronary heart disease.
Lecithin Cholesterol Acyltransferase Deficiency
LCAT Enzyme Replacement Therapy Reduces LpX and Improves Kidney Function in a Mouse Model of Familial LCAT Deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Lecithin cholesterol acyltransferase deficiency protects from diet-induced insulin resistance and obesity--novel insights from mouse models.
Lecithin Cholesterol Acyltransferase Deficiency
Lecithin cholesterol acyltransferase deficiency: ultrastructural examination of sequential renal biopsies.
Lecithin Cholesterol Acyltransferase Deficiency
Lecithin: cholesterol acyltransferase deficiency: identification of two defective alleles in fibroblast cDNA.
Lecithin Cholesterol Acyltransferase Deficiency
Lecithin: cholesterol acyltransferase--from biochemistry to role in cardiovascular disease.
Lecithin Cholesterol Acyltransferase Deficiency
Lecithin:Cholesterol Acyltransferase Activation by Sulfhydryl-Reactive Small Molecules: Role of Cysteine-31.
Lecithin Cholesterol Acyltransferase Deficiency
Lecithin:cholesterol acyltransferase deficiency and cell membrane lipids and function in human liver disease.
Lecithin Cholesterol Acyltransferase Deficiency
Lecithin:cholesterol acyltransferase deficiency associated with hepatic schistosomiasis mansoni.
Lecithin Cholesterol Acyltransferase Deficiency
Lecithin:cholesterol acyltransferase deficiency increases atherosclerosis in the low density lipoprotein receptor and apolipoprotein E knockout mice.
Lecithin Cholesterol Acyltransferase Deficiency
Lecithin:cholesterol acyltransferase deficiency protects against cholesterol-induced hepatic endoplasmic reticulum stress in mice.
Lecithin Cholesterol Acyltransferase Deficiency
Lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Lecithin:cholesterol acyltransferase deficiency: identification of a causative gene mutation and a co-inherited protein polymorphism.
Lecithin Cholesterol Acyltransferase Deficiency
Lipid and lipoprotein abnormalities in liver disease: the possible role of lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Lipoprotein abnormalities in galactosamine hepatitis: a model of experimental lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Lipoprotein and lecithin: cholesterol acyltransferase changes in galactosamine-induced rat liver injury.
Lecithin Cholesterol Acyltransferase Deficiency
Lipoprotein subfractions highly associated with renal damage in familial lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Long-term follow-up of a patient with lecithin cholesterol acyltransferase deficiency syndrome after kidney transplantation.
Lecithin Cholesterol Acyltransferase Deficiency
Lp8 is potentially associated with partial lecithin:cholesterol acyltransferase deficiency in a patient with primary biliary cirrhosis.
Lecithin Cholesterol Acyltransferase Deficiency
Management of lipoprotein X and its complications in a patient with primary sclerosing cholangitis.
Lecithin Cholesterol Acyltransferase Deficiency
Marked atherosclerosis in a patient with familiar lecithin: cholesterol acyltransferase deficiency associated with end-stage renal disease and diabetes mellitus.
Lecithin Cholesterol Acyltransferase Deficiency
Marked HDL deficiency and premature coronary heart disease.
Lecithin Cholesterol Acyltransferase Deficiency
Markedly accelerated catabolism of apolipoprotein A-II (ApoA-II) and high density lipoproteins containing ApoA-II in classic lecithin: cholesterol acyltransferase deficiency and fish-eye disease.
Lecithin Cholesterol Acyltransferase Deficiency
Molecular basis for activation of lecithin:cholesterol acyltransferase by a compound that increases HDL cholesterol.
Lecithin Cholesterol Acyltransferase Deficiency
Molecular diagnosis of lecithin: cholesterol acyltransferase deficiency in a presymptomatic proband.
Lecithin Cholesterol Acyltransferase Deficiency
Molecular pathways in the transformation of model discoidal lipoprotein complexes induced by lecithin:cholesterol acyltransferase.
Lecithin Cholesterol Acyltransferase Deficiency
Net lipid transfer between lipoproteins in fish-eye disease plasma supplemented with normal high density lipoproteins.
Lecithin Cholesterol Acyltransferase Deficiency
New in-vivo techniques for measuring lipoprotein metabolism.
Lecithin Cholesterol Acyltransferase Deficiency
Normalization of high density lipoprotein in fish eye disease plasma by purified normal human lecithin: cholesterol acyltransferase.
Lecithin Cholesterol Acyltransferase Deficiency
Novel Missense LCAT Gene Mutation Associated with an Atypical Phenotype of Familial LCAT Deficiency in Two Portuguese Brothers.
Lecithin Cholesterol Acyltransferase Deficiency
Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin:cholesterol acyltransferase deficiency and hypobetalipoproteinemia.
Lecithin Cholesterol Acyltransferase Deficiency
Ocular and Genetic Characteristics Observed in Two Cases of Fish-Eye Disease.
Lecithin Cholesterol Acyltransferase Deficiency
Ocular manifestations in familial lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Ophthalmic observations in lecithin cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Paradoxical esterification of plasma cholesterol in fish eye disease.
Lecithin Cholesterol Acyltransferase Deficiency
Plasma beta-2-microglobulin and urinary albumin: creatinine ratio in lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Plasma lipoprotein abnormalities in heterozygotes for familial lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Plasma lipoprotein alterations and morphologic changes with lipid deposition in the kidney of patients with hepatorenal syndrome.
Lecithin Cholesterol Acyltransferase Deficiency
Plasma lipoprotein metabolism in familial lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Plasma lipoproteins in familial lecithin: cholesterol acyltransferase deficiency. Further studies of very low and low density lipoprotein abnormalities.
Lecithin Cholesterol Acyltransferase Deficiency
Plasma lipoproteins in familial lecithin: cholesterol acyltransferase deficiency: effects of dietary manipulation.
Lecithin Cholesterol Acyltransferase Deficiency
Plasma lipoproteins in familial lecithin: cholesterol acyltransferase deficiency: effects of incubation with lecithin: cholesterol acyltransferase in vitro.
Lecithin Cholesterol Acyltransferase Deficiency
Plasma lipoproteins in familial lecithin: cholesterol acyltransferase deficiency: lipid composition and reactivity in vitro.
Lecithin Cholesterol Acyltransferase Deficiency
Plasma lipoproteins in familial lecithin: cholesterol acyltransferase deficiency: physical and chemical studies of low and high density lipoproteins.
Lecithin Cholesterol Acyltransferase Deficiency
Plasma lipoproteins in familial lecithin: cholesterol acyltransferase deficiency: structure of low and high density lipoproteins as revealed by elctron microscopy.
Lecithin Cholesterol Acyltransferase Deficiency
Plasma lipoproteins in patients with familial plasma lecithin: cholesterol acyltransferase deficiency: apolipoprotein composition of isolated fractions.
Lecithin Cholesterol Acyltransferase Deficiency
Point mutations in apolipoprotein A-I mimic the phenotype observed in patients with classical lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Possible association between an abnormal low density lipoprotein and nephropathy in lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Possible induction of renal dysfunction in patients with lecithin:cholesterol acyltransferase deficiency by oxidized phosphatidylcholine in glomeruli.
Lecithin Cholesterol Acyltransferase Deficiency
Prebeta-migrating high density lipoprotein: quantitation in normal and hyperlipidemic plasma by solid phase radioimmunoassay following electrophoretic transfer.
Lecithin Cholesterol Acyltransferase Deficiency
Presence of (alpha)-1-lipoprotein in patients with familial plasma lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Promotion of sterol efflux and net transport by apolipoprotein E in lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Quantitative studies of lipoprotein-X in familial lecithin: cholesterol acyltransferase deficiency and during cholesterol esterification.
Lecithin Cholesterol Acyltransferase Deficiency
Rapid electrophoretic separation of pre-beta-migrating high density lipoproteins using automated PhastSystem: application to analysis of lecithin:cholesterol acyltransferase-deficient plasma.
Lecithin Cholesterol Acyltransferase Deficiency
Recognizing familial lecithin cholesterol acyltransferase deficiency at the slit lamp.
Lecithin Cholesterol Acyltransferase Deficiency
Recombinant lecithin:cholesterol acyltransferase containing a Thr123-->Ile mutation esterifies cholesterol in low density lipoprotein but not in high density lipoprotein.
Lecithin Cholesterol Acyltransferase Deficiency
Recurrence of lecithin cholesterol acyltransferase deficiency after kidney transplantation.
Lecithin Cholesterol Acyltransferase Deficiency
Recurrent glomerulopathy in a renal allograft due to lecithin cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Relationship between structure and biochemical phenotype of lecithin:cholesterol acyltransferase (LCAT) mutants causing fish-eye disease.
Lecithin Cholesterol Acyltransferase Deficiency
Renal failure in familial lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Renal lipidosis associated with arteriohepatic dysplasia (Alagille's syndrome).
Lecithin Cholesterol Acyltransferase Deficiency
Reverse cholesterol transport in plasma of patients with different forms of familial HDL deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Sea-blue histiocytes in familial lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Self-adaptive modification of red-cell membrane lipids in lecithin: cholesterol acyltransferase deficiency. Lipid analysis and spin labeling.
Lecithin Cholesterol Acyltransferase Deficiency
Spin label studies of erythrocytes with abnormal lipid composition: comparison of red cells in a hereditary hemolytic syndrome and lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Splanchnic production of discoidal plasma high-density lipoprotein in man.
Lecithin Cholesterol Acyltransferase Deficiency
Structural and functional properties of two mutants of lecithin-cholesterol acyltransferase (T123I and N228K).
Lecithin Cholesterol Acyltransferase Deficiency
Structural differences between wild-type and fish eye disease mutant of lecithin:cholesterol acyltransferase.
Lecithin Cholesterol Acyltransferase Deficiency
Structural studies on serum lipoproteins in homozygotes and heterozygotes for the lecithin:cholesterol acyltransferase deficiency gene.
Lecithin Cholesterol Acyltransferase Deficiency
Studies on the pre-alpha-lipoprotein in patients with familial lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Studies on the protein moiety of serum high density lipoprotein from patients with familial lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Study of the components of reverse cholesterol transport in lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Substrate specificity of lecithin:cholesterol acyltransferase. Esterification of desmosterol, b-sitosterol, and cholecalciferol in human plasma.
Lecithin Cholesterol Acyltransferase Deficiency
Successful renal transplantation in a patient with familial lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
T-->G or T-->A mutation introduced in the branchpoint consensus sequence of intron 4 of lecithin:cholesterol acyltransferase (LCAT) gene: intron retention causing LCAT deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
T13M mutation of lecithin-cholesterol acyltransferase gene causes fish-eye disease.
Lecithin Cholesterol Acyltransferase Deficiency
Targeted disruption of the mouse lecithin:cholesterol acyltransferase (LCAT) gene. Generation of a new animal model for human LCAT deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
The basic apolipoprotein A-I in the patients with familial lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
The characterization of lipoproteins in the high density fraction obtained from patients with familial lecithin:cholesterol acyltransferase deficiency and their interaction with cultured human fibroblasts.
Lecithin Cholesterol Acyltransferase Deficiency
The effect of plasma transfusion on the plasma cholesterol esters in patients with familial plasma lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
The genetic defect of the original Norwegian lecithin:cholesterol acyltransferase deficiency families.
Lecithin Cholesterol Acyltransferase Deficiency
The influence of plasma from patients with familial plasma lecithin: cholesterol acyltransferase deficiency on the lipid pattern of erythrocytes.
Lecithin Cholesterol Acyltransferase Deficiency
The lipemia in familial plasma lecithin: cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families.
Lecithin Cholesterol Acyltransferase Deficiency
The role of lecithin:cholesterol acyltransferase deficiency in the apoprotein metabolism of alcoholic hepatitis.
Lecithin Cholesterol Acyltransferase Deficiency
The ultrastructure of plasma lipoproteins in lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Transmission of two novel mutations in a pedigree with familial lecithin:cholesterol acyltransferase deficiency: structure-function relationships and studies in a compound heterozygous proband.
Lecithin Cholesterol Acyltransferase Deficiency
Two different allelic mutations in a Finnish family with lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
Two different allelic mutations in the lecithin:cholesterol acyltransferase (LCAT) gene resulting in classic LCAT deficiency: LCAT (tyr83-->stop) and LCAT (tyr156-->asn).
Lecithin Cholesterol Acyltransferase Deficiency
Two novel frame shift mutations in lecithin:cholesterol acyltransferase (LCAT) gene associated with a familial LCAT deficiency phenotype.
Lecithin Cholesterol Acyltransferase Deficiency
Two novel molecular defects in the LCAT gene are associated with fish eye disease.
Lecithin Cholesterol Acyltransferase Deficiency
Two novel mutations of lecithin:cholesterol acyltransferase (LCAT) gene and the influence of APOE genotypes on clinical manifestations.
Lecithin Cholesterol Acyltransferase Deficiency
Two novel point mutations in the lecithin:cholesterol acyltransferase (LCAT) gene resulting in LCAT deficiency: LCAT (G873 deletion) and LCAT (Gly344-->Ser).
Lecithin Cholesterol Acyltransferase Deficiency
Unusual lipid composition of erythrocytes from the insectivorous bat Molossus molossus.
Lecithin Cholesterol Acyltransferase Deficiency
Unusual renal biopsy findings in a patient with familial lecithin:cholesterol acyltransferase deficiency.
Lecithin Cholesterol Acyltransferase Deficiency
[A case of familial lecithin: cholesterol acyltransferase deficiency]
Lecithin Cholesterol Acyltransferase Deficiency
[Atherosclerosis and sensitive determination of oxidized LDL using monoclonal antibody]
Lecithin Cholesterol Acyltransferase Deficiency
[Case of familial lecithin: cholesterol acyltransferase deficiency]
Lecithin Cholesterol Acyltransferase Deficiency
[Characteristics of red cell membrane disorders in the Japanese population]
Lecithin Cholesterol Acyltransferase Deficiency
[Familial alpha lipoprotein deficiency. Tangier disease, familial hypoalphalipoproteinemia and familial deficiency of lecithin cholesterol acyltransferase deficiency]
Lecithin Cholesterol Acyltransferase Deficiency
[Familial hypoalphalipoproteinemia. Vergani's disease]
Lecithin Cholesterol Acyltransferase Deficiency
[Familial lecithin cholesterol acyltransferase deficiency]
Lecithin Cholesterol Acyltransferase Deficiency
[Lecithin-cholesterol acyltransferase deficiency and fish eye disease]
Lecithin Cholesterol Acyltransferase Deficiency
[Lecithin: cholesterol acyltransferase (LCAT)--the genetic analysis of familial LCAT deficiency and fish eye disease]
Leptospirosis
Biomechanical and biochemical investigation of erythrocytes in late stage human leptospirosis.
lipoprotein lipase deficiency
Concentrations of electrophoretic and size subclasses of apolipoprotein A-I-containing particles in human peripheral lymph.
Liver Cirrhosis
Altered lipid composition and differential changes in activities of membrane-bound enzymes of erythrocytes in hepatic cirrhosis.
Liver Cirrhosis
Immunoaffinity-isolation of plasma lecithin-cholesterol acyltransferase (LCAT) from patients with hepatic cirrhosis.
Liver Cirrhosis
Lipoproteins, HDL-apolipoproteins, activities of hepatic lipase and lecithin-cholesterol acyltransferase in the plasma of patients with post-alcoholic end-stage liver cirrhosis.
Liver Cirrhosis
Serum apoproteins A and B and the lecithin: cholesterol acyl transferase activities in liver cirrhosis and hepatic coma patients.
Liver Cirrhosis, Biliary
Characterization of guinea pig plasma lipoproteins: the appearance of new lipoproteins in response to dietary cholesterol.
Liver Cirrhosis, Biliary
Lipoprotein abnormalities in patients with early primary biliary cirrhosis.
Liver Cirrhosis, Biliary
Lp8 is potentially associated with partial lecithin:cholesterol acyltransferase deficiency in a patient with primary biliary cirrhosis.
Liver Cirrhosis, Biliary
Management of lipoprotein X and its complications in a patient with primary sclerosing cholangitis.
Liver Cirrhosis, Biliary
The electrophoretic mobility of lipoprotein X in postheparin plasma.
Liver Diseases
A critical examination of the value of combined determinations of lecithin:cholesterol acyltransferase and lipoprotein-X in the differential diagnosis of liver disease.
Liver Diseases
Effectiveness of orthotopic liver transplantation on the restoration of cholesterol metabolism in patients with end-stage liver disease.
Liver Diseases
In vivo evaluation of lipoprotein cholesterol ester metabolism in patients with liver disease.
Liver Diseases
Lecithin-cholesterol acyltransferase and lipid transfer protein activities in liver disease.
Liver Diseases
Lecithin-cholesterol acyltransferase and the lipoprotein abnormalities of parenchymal liver disease.
Liver Diseases
Lecithin: cholesterol acyltransferase activity in patients with chronic liver diseases and positive LP-X tests.
Liver Diseases
Lecithin:cholesterol acyltransferase as a component of enzyme patterns in acute and chronic liver disease. A preliminary report.
Liver Diseases
Lecithin:cholesterol acyltransferase deficiency and cell membrane lipids and function in human liver disease.
Liver Diseases
Lipid and lipoprotein abnormalities in liver disease: the possible role of lecithin: cholesterol acyltransferase deficiency.
Liver Diseases
Liver tissue lecithin: cholesterol acyltransferase activity in patients with liver disease.
Liver Diseases
Plasma lecithin-cholesterol acyltransferase and erythrocyte lipids in liver disease.
Liver Diseases
Plasma lecithin: cholesterol acyltransferase activity in liver disease.
Liver Diseases
Plasma lecithin:cholesterol acyltransferase activity and the lipoprotein abnormalities of liver disease.
Liver Diseases
Plasma lecithin:cholesterol acyltransferase and phospholipid transfer protein activity independently associate with nonalcoholic fatty liver disease.
Liver Diseases
Red cell lipids in liver disease: relationship to serum lipids and to lecithin-cholesterol acyltransferase.
Liver Diseases
Role of lecithin:cholesterol acyltransferase and apolipoprotein A-I in cholesterol esterification in lipoprotein-X in vitro.
Liver Diseases
Serum cholesterol esterification in human liver disease: role of lecithin-cholesterol acyltransferase and cholesterol ester hydrolase.
Liver Diseases
Serum cholesterol esterification in liver disease. Combined determinations of lecithin: cholesterol acyltransferase and lipoprotein-X.
Liver Diseases
Similar behaviour of lecithin:cholesterol acyltransferase and pseudocholinesterase in liver disease and hyperlipoproteinemia.
Liver Diseases
The influence of LP-X and other lipoproteins associated with hepatic dysfunction on the activity of lecithin:cholesterol acyltransferase.
Liver Diseases
[Clinical significance of the changes in serum lecithin-cholesterol acyltransferase activity and lipids in patients with liver disease]
Liver Diseases
[Determination and clinical significance of plasma lecithin cholesterol acyltransferase activity in liver diseases (author's transl)]
Liver Diseases
[Plasma lecithin-cholesterol acyltransferase activity (LCAT) in late schistosomiasis and chronic liver disease]
Liver Diseases, Alcoholic
Abnormal plasma lipoproteins and lecithin-cholesterol acyltransferase deficiency in alcoholic liver disease.
Liver Diseases, Alcoholic
Radioisotopic assay of lecithin: cholesterol acyltransferase (LCAT) in alcoholic liver diseases: effects of alcohol withdrawal in the LCAT activity.
Lymphoma, Non-Hodgkin
Severe high-density lipoprotein deficiency associated with autoantibodies against lecithin:cholesterol acyltransferase in non-Hodgkin lymphoma.
Malaria
Alterations of lecithin-cholesterol acyltransferase activity during Plasmodium chabaudi rodent malaria.
Massive Hepatic Necrosis
Plasma lecithin: cholesterol acyltransferase activity in liver disease.
Metabolic Diseases
Familial lecithin:cholesterol acyltransferase deficiency - a new metabolic disease with renal involvement.
Metabolic Diseases
Lecithin:Cholesterol Acyltransferase (LCAT) Deficiency: Renal Lesions with Early Graft Recurrence.
Metabolic Syndrome
Plasma lecithin: cholesterol acyltransferase activity is elevated in metabolic syndrome and is an independent marker of increased carotid artery intima media thickness.
Metabolic Syndrome
[The lipoprotein metabolism in arterial hypertension, type II diabetes mellitus, and metabolic syndrome]
Multiple Sclerosis
Lecithin cholesterol acyltransferase in human cerebrospinal fluid: reduced level in patients with multiple sclerosis and evidence of direct synthesis in the brain.
Multiple Sclerosis
Lecithin:cholesterol acyltransferase activity in plasma of patients with multiple sclerosis.
Myocardial Infarction
Alterations in plasma lecithin:cholesterol acyltransferase and myeloperoxidase in acute myocardial infarction: Implications for cardiac outcome.
Myocardial Infarction
Effects of smoking on HDL subfractions in myocardial infarction patients: effects on lecithin-cholesterol acyltransferase and hepatic lipase.
Myocardial Infarction
Lecithin:cholesterol acyltransferase activity in patients with acute myocardial infarction and coronary heart disease.
Myocardial Infarction
[Interrelation of cholesterol esters, phospholipids and lecithin cholesterol acyltransferase activity in the serum of men with myocardial infarction]
Myocardial Ischemia
High pre-beta1 HDL concentrations and low lecithin: cholesterol acyltransferase activities are strong positive risk markers for ischemic heart disease and independent of HDL-cholesterol.
Myocardial Ischemia
Lecithin:cholesterol acyltransferase as a possible diagnostic tool in ischemic heart disease.
Myocardial Ischemia
[Relationship between the activity of lecithin cholesterol acyltransferase, hyperlipoproteinemia type and the indicators of the system of hemostasis in chronic ischemic heart disease]
Neoplasms
Alterations in plasma lipoproteins and heparin-releasable lipase activities in mice bearing the GRSL ascites tumor.
Neoplasms
Corn silk extract improves cholesterol metabolism in C57BL/6J mouse fed high-fat diets.
Neoplasms
Effect of selenium on lipids and some lipid metabolising enzymes in DMBA induced mammary tumor rats.
Neoplasms
Efficacy of oral rosuvastatin intervention on HDL and its associated proteins in men with type 2 diabetes mellitus.
Neoplasms
Higher Cardiovascular Risk in Common Variable Immunodeficiency and X-Linked Agammaglobulinaemia Patients.
Neoplasms
Lipid composition and de novo cholesterogenesis in normal and neoplastic rat mammary tissues.
Neoplasms
Lipopolysaccharide and tumor necrosis factor cause a fall in plasma concentration of lecithin: cholesterol acyltransferase in cynomolgus monkeys.
Neoplasms
Preliminary assessment of differential expression of candidate genes associated with atherosclerosis.
Neoplasms
Tumor targeting effects of a novel modified paclitaxel-loaded discoidal mimic high density lipoproteins.
Nephritis, Hereditary
An aid to the diagnosis of genetic disorders underlying adult-onset renal failure: a literature review.
Nephrotic Syndrome
A 33-year-old man with nephrotic syndrome and lecithin-cholesterol acyltransferase (LCAT) deficiency. Description of two new mutations in the LCAT gene.
Nephrotic Syndrome
A case of congenital nephrotic syndrome associated with partial deficiency of lecithin cholesterol acyltransferase (LCAT) and hypothyroidism.
Nephrotic Syndrome
Abnormal acyltransferase activities and accelerated cholesteryl ester transfer in patients with nephrotic syndrome.
Nephrotic Syndrome
Abnormal lipoprotein and apolipoprotein pattern in lipoprotein glomerulopathy.
Nephrotic Syndrome
Acquired lecithin-cholesterol acyltransferase deficiency in nephrotic syndrome.
Nephrotic Syndrome
Acyl-coenzyme A:cholesterol acyltransferase inhibition ameliorates proteinuria, hyperlipidemia, lecithin-cholesterol acyltransferase, SRB-1, and low-denisty lipoprotein receptor deficiencies in nephrotic syndrome.
Nephrotic Syndrome
Immune-mediated acquired lecithin-cholesterol acyltransferase deficiency: A case report and literature review.
Nephrotic Syndrome
Lecithin cholesterol acyltransferase deficiency: ultrastructural examination of sequential renal biopsies.
Nephrotic Syndrome
Serum apolipoproteins A and B, lecithin: cholesterol acyl transferase activities and urinary cholesterol levels in nephrotic syndrome patients before and during steroid treatment.
Nephrotic Syndrome
[Lipoproteins, apolipoproteins, lipoprotein lipase, hepatic triglyceride lipase and lecithin cholesterol acyltransferase in patients with nephrotic syndrome]
Niemann-Pick Diseases
Structure and function of lamellar bodies, lipid-protein complexes involved in storage and secretion of cellular lipids.
Non-alcoholic Fatty Liver Disease
Plasma lecithin:cholesterol acyltransferase and phospholipid transfer protein activity independently associate with nonalcoholic fatty liver disease.
Obesity
Lecithin cholesterol acyltransferase (LCAT) null mice are protected from diet-induced obesity and insulin resistance in a gender specific manner through multiple pathways.
Obesity
Lecithin:Cholesterol Acyltransferase (LCAT) Deficiency Promotes Differentiation of Satellite Cells to Brown Adipocytes in a Cholesterol-dependent Manner.
Obesity
Lecithin:cholesterol acyltransferase activity, plasma and lipoprotein lipids and obesity in men and women.
Obesity
Lecithin:cholesterol acyltransferase deficiency protects against cholesterol-induced hepatic endoplasmic reticulum stress in mice.
Osteoporosis, Postmenopausal
Reduction of lecithin-cholesterol acyltransferase, apolipoprotein D and the Lp(a) lipoprotein with the anabolic steroid stanozolol.
Pancreatitis
Lecithin-cholesterol acyltransferase deficiency presenting with acute pancreatitis: effect of infusion of normal plasma on triglyceride-rich lipoproteins.
peptidyl-glutamate 4-carboxylase deficiency
Studies on inborn errors of metabolism in Norway.
Peripheral Nervous System Diseases
Familial lecithin: cholesterol acyltransferase deficiency complicated with unconjugated hyperbilirubinemia and peripheral neuropathy. The first reported cases in the Far East.
Peritonitis
Changes in the blood lipid-transporting system in rats over the first day of experimental peritonitis.
phosphatidylcholine-sterol o-acyltransferase deficiency
A case of acquired lecithin:cholesterol acyltransferase deficiency with sarcoidosis that remitted spontaneously.
phosphatidylcholine-sterol o-acyltransferase deficiency
A case of familial lecithin-cholesterol acyltransferase deficiency on hemodialysis for over 20 years.
phosphatidylcholine-sterol o-acyltransferase deficiency
A new case of familial LCAT deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
A novel homozygous mutation causing lecithin-cholesterol acyltransferase deficiency in a proband of Romanian origin with a record of extreme gestational hyperlipidemia.
phosphatidylcholine-sterol o-acyltransferase deficiency
A review on lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
A study of the small spherical high density lipoproteins of patients afflicted with familial lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
A study of the structure of the gene for lecithin: cholesterol acyltransferase in four unrelated individuals with familial lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Abnormal lipoprotein appearing in plasma of patients who received a ten percent soybean oil emulsion infusion.
phosphatidylcholine-sterol o-acyltransferase deficiency
Abnormal plasma lipoproteins and lecithin-cholesterol acyltransferase deficiency in alcoholic liver disease.
phosphatidylcholine-sterol o-acyltransferase deficiency
Abnormalities in lipoproteins of d < 1.006 g/ml in familial lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Abnormalities in plasma lipoprotein in familial partial lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Acquired lecithin-cholesterol acyltransferase deficiency in nephrotic syndrome.
phosphatidylcholine-sterol o-acyltransferase deficiency
Acquired lecithin:cholesterol acyltransferase deficiency as a major factor in lowering plasma HDL levels in chronic kidney disease.
phosphatidylcholine-sterol o-acyltransferase deficiency
Activation of lipoprotein lipase by lipoprotein fractions of human serum.
phosphatidylcholine-sterol o-acyltransferase deficiency
Administration of the High-Density Lipoprotein Mimetic CER-001 for Inherited Lecithin-Cholesterol Acyltransferase Deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Amino acid composition of serum high density lipoprotein in patients with familial lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
An aid to the diagnosis of genetic disorders underlying adult-onset renal failure: a literature review.
phosphatidylcholine-sterol o-acyltransferase deficiency
An unusual case of nephrotic syndrome.
phosphatidylcholine-sterol o-acyltransferase deficiency
ApoA-II expression in CETP transgenic mice increases VLDL production and impairs VLDL clearance.
phosphatidylcholine-sterol o-acyltransferase deficiency
Apolipoprotein AIMilano. Partial lecithin:cholesterol acyltransferase deficiency due to low levels of a functional enzyme.
phosphatidylcholine-sterol o-acyltransferase deficiency
Apolipoprotein and lipid distribution between vesicles and HDL-like particles formed during lipolysis of human very low density lipoproteins by perfused rat heart.
phosphatidylcholine-sterol o-acyltransferase deficiency
Apolipoproteins and lipoprotein families in familial lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Approach to the patient with extremely low HDL-cholesterol.
phosphatidylcholine-sterol o-acyltransferase deficiency
Cardiac surgery for a patient with familial lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Case Report: Management of Corneal Clouding from Lecithin: Cholesterol Acyltransferase Deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Causes of dysregulation of lipid metabolism in chronic renal failure.
phosphatidylcholine-sterol o-acyltransferase deficiency
Changes in lipoprotein profile and urinary albumin excretion in familial LCAT deficiency with lipid lowering therapy.
phosphatidylcholine-sterol o-acyltransferase deficiency
Characterization of apolipoprotein E-rich high density lipoproteins in familial lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Characterization of guinea pig plasma lipoproteins: the appearance of new lipoproteins in response to dietary cholesterol.
phosphatidylcholine-sterol o-acyltransferase deficiency
Characterization of subspecies of apolipoprotein A-I-containing lipoprotein in homozygotes for familial lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Characterization of subspecies of lipoprotein containing apolipoprotein A-I in heterozygotes for familial lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Cholesteryl ester storage disease with secondary lecithin cholesterol acyl transferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Clinical variant of Tangier disease in Japan: mutation of the ABCA1 gene in hypoalphalipoproteinemia with corneal lipidosis.
phosphatidylcholine-sterol o-acyltransferase deficiency
Clinical, biochemical, and genetic features in familial disorders of high density lipoprotein deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Co-existence of classic familial lecithin-cholesterol acyl transferase deficiency and fish eye disease in the same family.
phosphatidylcholine-sterol o-acyltransferase deficiency
Combined liver-kidney transplantation for rare diseases.
phosphatidylcholine-sterol o-acyltransferase deficiency
Concentrations of electrophoretic and size subclasses of apolipoprotein A-I-containing particles in human peripheral lymph.
phosphatidylcholine-sterol o-acyltransferase deficiency
Controversy over the atherogenicity of lipoprotein-X.
phosphatidylcholine-sterol o-acyltransferase deficiency
Corneal Clouding in a Young Woman With Low HDL Cholesterol.
phosphatidylcholine-sterol o-acyltransferase deficiency
Corticosteroid treatment of kidney disease in a patient with familial lecithin-cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Decreased sodium influx and abnormal red cell membrane lipids in a patient with familial plasma lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Defective enzyme causes lecithin-cholesterol acyltransferase deficiency in a Japanese kindred.
phosphatidylcholine-sterol o-acyltransferase deficiency
Demonstration of intact intracellular cholesterol esterification and normal low-density lipoprotein pathway in fibroblasts from a patient with lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Detection of erythrocyte membrane structural abnormalities in lecithin: cholesterol acyltransferase deficiency using a spin label approach.
phosphatidylcholine-sterol o-acyltransferase deficiency
Determination of apolipoprotein A and its constitutive A-I and A-II polypeptides by separate electroimmunoassays.
phosphatidylcholine-sterol o-acyltransferase deficiency
Differential diagnosis of Schnyder corneal dystrophy.
phosphatidylcholine-sterol o-acyltransferase deficiency
Differential phenotypic expression by three mutant alleles in familial lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Discrepancies between lipoprotein(a) concentrations in icteric sera measured by immunonephelometry and electroimmunodiffusion.
phosphatidylcholine-sterol o-acyltransferase deficiency
Effect of early enteral feeding on apolipoprotein AI levels and high-density lipoprotein heterogeneity in preterm infants.
phosphatidylcholine-sterol o-acyltransferase deficiency
Effects of plasma infusion on plasma lipids, apoproteins and plasma enzyme activities in familial lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Endocrine Dysfunctions in Patients with Inherited Metabolic Diseases.
phosphatidylcholine-sterol o-acyltransferase deficiency
Enzymic esterification of cholesterol in rat intestinal mucosa catalyzed by acyl-CoA: cholesterol acyltransferase.
phosphatidylcholine-sterol o-acyltransferase deficiency
Erythrocyte membrane alterations in lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Evidence for impaired cellular cholesterol removal mediated by apo A-I containing lipoproteins in patients with familial lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial Lecithin Cholesterol Acyl Transferase Deficiency with Chronic Kidney Disease.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial lecithin-cholesterol acyltransferase deficiency in a Japanese family: evidence for functionally defective enzyme in homozygotes and obligate heterozygotes.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial lecithin-cholesterol acyltransferase deficiency in four Norwegian Families. Evidence for low levels of a functionally defective enzyme.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial lecithin-cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial lecithin-cholesterol acyltransferase deficiency: biochemical characteristics and molecular analysis of a new LCAT mutation in a Polish family.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial lecithin: cholesterol acyltransferase deficiency complicated with unconjugated hyperbilirubinemia and peripheral neuropathy. The first reported cases in the Far East.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial lecithin: cholesterol acyltransferase deficiency. Study of two new patients and their close relatives.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial lecithin:cholesterol acyltransferase deficiency - a new metabolic disease with renal involvement.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial Lecithin:cholesterol acyltransferase deficiency with renal failure in two siblings. First case report from India.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial lecithin:cholesterol acyltransferase deficiency. Biochemistry of the cornea.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial lecithin:cholesterol acyltransferase deficiency. Further studies on plasma lipoproteins and plasma postheparin lipase activity of a patient with normal renal function.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial lecithin:cholesterol acyltransferase deficiency. Report of a fourth family from northwestern Norway.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial lecithin:cholesterol acyltransferase deficiency. Report of a third Norwegian family with two afflicted members.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial lecithin:cholesterol acyltransferase deficiency. Studies on lipid composition and morphology of tissues.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial lecithin:cholesterol acyltransferase deficiency. Ultrastructural studies on lipid deposition and tissue reactions.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial lecithin:cholesterol acyltransferase deficiency: First-in-human treatment with enzyme replacement.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial lecithin:cholesterol acyltransferase deficiency: further resolution of lipoprotein particle heterogeneity in the low density interval.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial lecithin:cholesterol acyltransferase deficiency: molecular analysis of a compound heterozygote: LCAT (Arg147 --> Trp) and LCAT (Tyr171 --> Stop).
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial plasma lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial plasma lecithin: cholesterol acyltransferase deficiency. A new family with partial LCAT activity.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial plasma lecithin: cholesterol acyltransferase deficiency. A study of the platelets.
phosphatidylcholine-sterol o-acyltransferase deficiency
Familial splenomegaly: macrophage hypercatabolism of lipoproteins associated with apolipoprotein E mutation [apolipoprotein E (delta149 Leu)].
phosphatidylcholine-sterol o-acyltransferase deficiency
Free cholesterol deposition in the cornea of human apolipoprotein A-II transgenic mice with functional lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Functional lecithin:cholesterol acyltransferase deficiency and high density lipoprotein deficiency in transgenic mice overexpressing human apolipoprotein A-II.
phosphatidylcholine-sterol o-acyltransferase deficiency
Gene therapy for dyslipidemia: clinical prospects.
phosphatidylcholine-sterol o-acyltransferase deficiency
Genetic lecithin:cholesterol acyltransferase deficiency and cardiovascular disease.
phosphatidylcholine-sterol o-acyltransferase deficiency
Glomerular mesangiolipidosis in Alagille syndrome (arteriohepatic dysplasia).
phosphatidylcholine-sterol o-acyltransferase deficiency
HDL and type 2 diabetes: the chicken or the egg?
phosphatidylcholine-sterol o-acyltransferase deficiency
Hereditary lecithin cholesterol acyltransferase deficiency. Report of a new family with two afflicted sisters.
phosphatidylcholine-sterol o-acyltransferase deficiency
Hereditary lecithin-cholesterol acyltransferase deficiency and Bloom syndrome in the same individual.
phosphatidylcholine-sterol o-acyltransferase deficiency
Hereditary lecithin-cholesterol acyltransferase deficiency. Case report of a German patient.
phosphatidylcholine-sterol o-acyltransferase deficiency
Hereditary lecithin-cholesterol acyltransferase deficiency. Report of 2 new cases and review of the literature.
phosphatidylcholine-sterol o-acyltransferase deficiency
Hereditary plasma lecithin-cholesterol acyl transferase deficiency: a heterozygous variant with erythrocyte membrane abnormalities.
phosphatidylcholine-sterol o-acyltransferase deficiency
Heterogeneity of nascent high density lipoproteins secreted by the hepatoma-derived cell line, Hep G2.
phosphatidylcholine-sterol o-acyltransferase deficiency
Histiocytic and Nonhistiocytic Glomerular Lesions: Foam Cells and Their Mimickers.
phosphatidylcholine-sterol o-acyltransferase deficiency
Histopathology of corneal changes in lecithin-cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Human lecithin:cholesterol acyltransferase deficiency: in vivo kinetics of low-density lipoprotein and lipoprotein-X.
phosphatidylcholine-sterol o-acyltransferase deficiency
Hypertriglyceridemia in lecithin-cholesterol acyltransferase-deficient mice is associated with hepatic overproduction of triglycerides, increased lipogenesis, and improved glucose tolerance.
phosphatidylcholine-sterol o-acyltransferase deficiency
Hypocomplementemic type II membranoproliferative glomerulonephritis in a male patient with familial lecithin-cholesterol acyltransferase deficiency due to two different allelic mutations.
phosphatidylcholine-sterol o-acyltransferase deficiency
Identification of lipoprotein families in familial lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Identification of the abnormal cholestatic lipoprotein (LP-X) in familial lecithin:Cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Immune-mediated acquired lecithin-cholesterol acyltransferase deficiency: A case report and literature review.
phosphatidylcholine-sterol o-acyltransferase deficiency
In vitro effects of lecithin:cholesterol acyltransferase on apolipoprotein distribution in familial lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
In Vivo Imaging of the Cornea in a Patient with Lecithin-Cholesterol Acyltransferase Deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
In vivo imaging of the cornea in a patient with lecithin-cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Isolated low HDL-cholesterol as an important risk factor for coronary heart disease.
phosphatidylcholine-sterol o-acyltransferase deficiency
Lecithin cholesterol acyl transferase deficiency. Light and electron microscopic finding from two corneas.
phosphatidylcholine-sterol o-acyltransferase deficiency
Lecithin cholesterol acyl transferase deficiency: molecular analysis of a mutated allele.
phosphatidylcholine-sterol o-acyltransferase deficiency
Lecithin cholesterol acyltransferase deficiency protects from diet-induced insulin resistance and obesity--novel insights from mouse models.
phosphatidylcholine-sterol o-acyltransferase deficiency
Lecithin cholesterol acyltransferase deficiency: ultrastructural examination of sequential renal biopsies.
phosphatidylcholine-sterol o-acyltransferase deficiency
Lecithin-cholesterol acyltransferase deficiency presenting with acute pancreatitis: effect of infusion of normal plasma on triglyceride-rich lipoproteins.
phosphatidylcholine-sterol o-acyltransferase deficiency
Lecithin-cholesterol acyltransferase deficiency: first report of case in a United States citizen.
phosphatidylcholine-sterol o-acyltransferase deficiency
Lecithin: cholesterol acyltransferase deficiency: identification of two defective alleles in fibroblast cDNA.
phosphatidylcholine-sterol o-acyltransferase deficiency
Lecithin:Cholesterol Acyltransferase Activation by Sulfhydryl-Reactive Small Molecules: Role of Cysteine-31.
phosphatidylcholine-sterol o-acyltransferase deficiency
Lecithin:cholesterol acyltransferase deficiency and cell membrane lipids and function in human liver disease.
phosphatidylcholine-sterol o-acyltransferase deficiency
Lecithin:cholesterol acyltransferase deficiency associated with hepatic schistosomiasis mansoni.
phosphatidylcholine-sterol o-acyltransferase deficiency
Lecithin:cholesterol acyltransferase deficiency increases atherosclerosis in the low density lipoprotein receptor and apolipoprotein E knockout mice.
phosphatidylcholine-sterol o-acyltransferase deficiency
Lecithin:cholesterol acyltransferase deficiency protects against cholesterol-induced hepatic endoplasmic reticulum stress in mice.
phosphatidylcholine-sterol o-acyltransferase deficiency
Lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Lecithin:cholesterol acyltransferase deficiency: identification of a causative gene mutation and a co-inherited protein polymorphism.
phosphatidylcholine-sterol o-acyltransferase deficiency
Lipid and lipoprotein abnormalities in liver disease: the possible role of lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Lipoprotein abnormalities in galactosamine hepatitis: a model of experimental lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Lipoprotein and lecithin: cholesterol acyltransferase changes in galactosamine-induced rat liver injury.
phosphatidylcholine-sterol o-acyltransferase deficiency
Lipoprotein subfractions highly associated with renal damage in familial lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Long-term follow-up of a patient with lecithin cholesterol acyltransferase deficiency syndrome after kidney transplantation.
phosphatidylcholine-sterol o-acyltransferase deficiency
Low density lipoprotein-activated lysolecithin acylation by human plasma lecithin-cholesterol acyltransferase. Identity of lysolecithin acyltransferase and lecithin-cholesterol acyltransferase.
phosphatidylcholine-sterol o-acyltransferase deficiency
Lp8 is potentially associated with partial lecithin:cholesterol acyltransferase deficiency in a patient with primary biliary cirrhosis.
phosphatidylcholine-sterol o-acyltransferase deficiency
Management of lipoprotein X and its complications in a patient with primary sclerosing cholangitis.
phosphatidylcholine-sterol o-acyltransferase deficiency
Marked atherosclerosis in a patient with familiar lecithin: cholesterol acyltransferase deficiency associated with end-stage renal disease and diabetes mellitus.
phosphatidylcholine-sterol o-acyltransferase deficiency
Marked HDL deficiency and premature coronary heart disease.
phosphatidylcholine-sterol o-acyltransferase deficiency
Markedly accelerated catabolism of apolipoprotein A-II (ApoA-II) and high density lipoproteins containing ApoA-II in classic lecithin: cholesterol acyltransferase deficiency and fish-eye disease.
phosphatidylcholine-sterol o-acyltransferase deficiency
Molecular diagnosis of lecithin: cholesterol acyltransferase deficiency in a presymptomatic proband.
phosphatidylcholine-sterol o-acyltransferase deficiency
Molecular pathways in the transformation of model discoidal lipoprotein complexes induced by lecithin:cholesterol acyltransferase.
phosphatidylcholine-sterol o-acyltransferase deficiency
Molecular species of phosphatidylcholine in familial lecithin-cholesterol acyltransferase deficiency: effect of enzyme supplementation.
phosphatidylcholine-sterol o-acyltransferase deficiency
Nephropathy of familial lecithin-cholesterol acyltransferase deficiency: report of a case.
phosphatidylcholine-sterol o-acyltransferase deficiency
New in-vivo techniques for measuring lipoprotein metabolism.
phosphatidylcholine-sterol o-acyltransferase deficiency
Novel Missense LCAT Gene Mutation Associated with an Atypical Phenotype of Familial LCAT Deficiency in Two Portuguese Brothers.
phosphatidylcholine-sterol o-acyltransferase deficiency
Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin:cholesterol acyltransferase deficiency and hypobetalipoproteinemia.
phosphatidylcholine-sterol o-acyltransferase deficiency
Ocular manifestations in familial lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Ophthalmic observations in lecithin cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Plasma beta-2-microglobulin and urinary albumin: creatinine ratio in lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Plasma lecithin-cholesterol acyltransferase deficiency in a child with terminal pulmonary hyaline membrane disease.
phosphatidylcholine-sterol o-acyltransferase deficiency
Plasma lipoprotein abnormalities in heterozygotes for familial lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Plasma lipoprotein alterations and morphologic changes with lipid deposition in the kidney of patients with hepatorenal syndrome.
phosphatidylcholine-sterol o-acyltransferase deficiency
Plasma lipoprotein metabolism in familial lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Plasma lipoproteins in familial lecithin: cholesterol acyltransferase deficiency. Further studies of very low and low density lipoprotein abnormalities.
phosphatidylcholine-sterol o-acyltransferase deficiency
Plasma lipoproteins in familial lecithin: cholesterol acyltransferase deficiency: effects of dietary manipulation.
phosphatidylcholine-sterol o-acyltransferase deficiency
Plasma lipoproteins in familial lecithin: cholesterol acyltransferase deficiency: effects of incubation with lecithin: cholesterol acyltransferase in vitro.
phosphatidylcholine-sterol o-acyltransferase deficiency
Plasma lipoproteins in familial lecithin: cholesterol acyltransferase deficiency: lipid composition and reactivity in vitro.
phosphatidylcholine-sterol o-acyltransferase deficiency
Plasma lipoproteins in familial lecithin: cholesterol acyltransferase deficiency: physical and chemical studies of low and high density lipoproteins.
phosphatidylcholine-sterol o-acyltransferase deficiency
Plasma lipoproteins in familial lecithin: cholesterol acyltransferase deficiency: structure of low and high density lipoproteins as revealed by elctron microscopy.
phosphatidylcholine-sterol o-acyltransferase deficiency
Plasma lipoproteins in patients with familial plasma lecithin: cholesterol acyltransferase deficiency: apolipoprotein composition of isolated fractions.
phosphatidylcholine-sterol o-acyltransferase deficiency
Point mutations in apolipoprotein A-I mimic the phenotype observed in patients with classical lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Possible association between an abnormal low density lipoprotein and nephropathy in lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Possible induction of renal dysfunction in patients with lecithin:cholesterol acyltransferase deficiency by oxidized phosphatidylcholine in glomeruli.
phosphatidylcholine-sterol o-acyltransferase deficiency
Postabsorptive retinyl palmitate removal is retarded in lecithin-cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Prebeta-migrating high density lipoprotein: quantitation in normal and hyperlipidemic plasma by solid phase radioimmunoassay following electrophoretic transfer.
phosphatidylcholine-sterol o-acyltransferase deficiency
Prematurity and lecithin-cholesterol acyltransferase deficiency in newborn infants.
phosphatidylcholine-sterol o-acyltransferase deficiency
Presence of (alpha)-1-lipoprotein in patients with familial plasma lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Probucol prevents early coronary heart disease and death in the high-density lipoprotein receptor SR-BI/apolipoprotein E double knockout mouse.
phosphatidylcholine-sterol o-acyltransferase deficiency
Promotion of sterol efflux and net transport by apolipoprotein E in lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Quantitative studies of lipoprotein-X in familial lecithin: cholesterol acyltransferase deficiency and during cholesterol esterification.
phosphatidylcholine-sterol o-acyltransferase deficiency
Rapid electrophoretic separation of pre-beta-migrating high density lipoproteins using automated PhastSystem: application to analysis of lecithin:cholesterol acyltransferase-deficient plasma.
phosphatidylcholine-sterol o-acyltransferase deficiency
Rapid normalization of severe hypercholesterolemia mediated by lipoprotein X after liver transplantation in a patient with cholestasis - a case report.
phosphatidylcholine-sterol o-acyltransferase deficiency
Recognizing familial lecithin cholesterol acyltransferase deficiency at the slit lamp.
phosphatidylcholine-sterol o-acyltransferase deficiency
Recurrence of lecithin cholesterol acyltransferase deficiency after kidney transplantation.
phosphatidylcholine-sterol o-acyltransferase deficiency
Recurrent glomerulopathy in a renal allograft due to lecithin cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Renal failure in familial lecithin-cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Renal failure in familial lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Renal lesions in familial lecithin-cholesterol acyltransferase deficiency. Ultrastructural heterogeneity of glomerular changes.
phosphatidylcholine-sterol o-acyltransferase deficiency
Renal lipidosis associated with arteriohepatic dysplasia (Alagille's syndrome).
phosphatidylcholine-sterol o-acyltransferase deficiency
Sea-blue histiocytes in familial lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Self-adaptive modification of red-cell membrane lipids in lecithin: cholesterol acyltransferase deficiency. Lipid analysis and spin labeling.
phosphatidylcholine-sterol o-acyltransferase deficiency
Spin label studies of erythrocytes with abnormal lipid composition: comparison of red cells in a hereditary hemolytic syndrome and lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Splanchnic production of discoidal plasma high-density lipoprotein in man.
phosphatidylcholine-sterol o-acyltransferase deficiency
Splenomegaly with sea-blue histiocytosis, dyslipidemia, and nephropathy in a patient with lecithin-cholesterol acyltransferase deficiency: a clinicopathologic correlation.
phosphatidylcholine-sterol o-acyltransferase deficiency
Structural studies on serum lipoproteins in homozygotes and heterozygotes for the lecithin:cholesterol acyltransferase deficiency gene.
phosphatidylcholine-sterol o-acyltransferase deficiency
Studies on inborn errors of metabolism in Norway.
phosphatidylcholine-sterol o-acyltransferase deficiency
Studies on the pre-alpha-lipoprotein in patients with familial lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Studies on the protein moiety of serum high density lipoprotein from patients with familial lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Study of the components of reverse cholesterol transport in lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Substrate specificity of lecithin:cholesterol acyltransferase. Esterification of desmosterol, b-sitosterol, and cholecalciferol in human plasma.
phosphatidylcholine-sterol o-acyltransferase deficiency
Successful renal transplantation in a patient with familial lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
The basic apolipoprotein A-I in the patients with familial lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
The characterization of lipoproteins in the high density fraction obtained from patients with familial lecithin:cholesterol acyltransferase deficiency and their interaction with cultured human fibroblasts.
phosphatidylcholine-sterol o-acyltransferase deficiency
The effect of plasma transfusion on the plasma cholesterol esters in patients with familial plasma lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
The genetic defect of the original Norwegian lecithin:cholesterol acyltransferase deficiency families.
phosphatidylcholine-sterol o-acyltransferase deficiency
The influence of plasma from patients with familial plasma lecithin: cholesterol acyltransferase deficiency on the lipid pattern of erythrocytes.
phosphatidylcholine-sterol o-acyltransferase deficiency
The lipemia in familial plasma lecithin: cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families.
phosphatidylcholine-sterol o-acyltransferase deficiency
The role of lecithin:cholesterol acyltransferase deficiency in the apoprotein metabolism of alcoholic hepatitis.
phosphatidylcholine-sterol o-acyltransferase deficiency
The ultrastructure of plasma lipoproteins in lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Transmission of two novel mutations in a pedigree with familial lecithin:cholesterol acyltransferase deficiency: structure-function relationships and studies in a compound heterozygous proband.
phosphatidylcholine-sterol o-acyltransferase deficiency
Two different allelic mutations in a Finnish family with lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Two novel mutations of lecithin:cholesterol acyltransferase (LCAT) gene and the influence of APOE genotypes on clinical manifestations.
phosphatidylcholine-sterol o-acyltransferase deficiency
Ultrastructural aspects of familial lecithin-cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
Undetectable high-density lipoprotein cholesterol in acute malaria.
phosphatidylcholine-sterol o-acyltransferase deficiency
Unusual lipid composition of erythrocytes from the insectivorous bat Molossus molossus.
phosphatidylcholine-sterol o-acyltransferase deficiency
Unusual renal biopsy findings in a patient with familial lecithin:cholesterol acyltransferase deficiency.
phosphatidylcholine-sterol o-acyltransferase deficiency
[A case of familial lecithin: cholesterol acyltransferase deficiency]
phosphatidylcholine-sterol o-acyltransferase deficiency
[Case of familial lecithin: cholesterol acyltransferase deficiency]
phosphatidylcholine-sterol o-acyltransferase deficiency
[Characteristics of red cell membrane disorders in the Japanese population]
phosphatidylcholine-sterol o-acyltransferase deficiency
[Clinical features of lecithin-cholesterol acyltransferase deficiency]
phosphatidylcholine-sterol o-acyltransferase deficiency
[Congenital lecithin-cholesterol acyltransferase deficiency. Description of a new case]
phosphatidylcholine-sterol o-acyltransferase deficiency
[Decreased sodium influx in leaky red cell membranes in familial lecithin-cholesterol acyltransferase deficiency]
phosphatidylcholine-sterol o-acyltransferase deficiency
[Familial alpha lipoprotein deficiency. Tangier disease, familial hypoalphalipoproteinemia and familial deficiency of lecithin cholesterol acyltransferase deficiency]
phosphatidylcholine-sterol o-acyltransferase deficiency
[Familial lecithin cholesterol acyltransferase deficiencies]
phosphatidylcholine-sterol o-acyltransferase deficiency
[Familial lecithin cholesterol acyltransferase deficiency]
phosphatidylcholine-sterol o-acyltransferase deficiency
[Familial lecithin-cholesterol acyltransferase deficiency]
phosphatidylcholine-sterol o-acyltransferase deficiency
[Lecithin-cholesterol acyltransferase deficiency and fish eye disease]
phosphatidylcholine-sterol o-acyltransferase deficiency
[Metabolic disorders and corneal changes (author's transl)]
Pneumonia
Decreased apolipoprotein C-III concentration in the high-density lipoprotein fraction from calves inoculated with Pasteurella haemolytica and bovine herpes virus-1.
Pneumonia
Reduction in serum lecithin:cholesterol acyltransferase activity in natural cases of pneumonia in calves.
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Lecithin cholesterol acyltransferase activity in acute lymphoblastic leukemia.
Proteinuria
Acyl-coenzyme A:cholesterol acyltransferase inhibition ameliorates proteinuria, hyperlipidemia, lecithin-cholesterol acyltransferase, SRB-1, and low-denisty lipoprotein receptor deficiencies in nephrotic syndrome.
Proteinuria
An unusual presentation of LCAT deficiency as nephrotic syndrome with normal serum HDL-C level.
Proteinuria
Characterization of a new LCAT mutation causing familial LCAT deficiency (FLD) and the role of APOE as a modifier gene of the FLD phenotype.
Proteinuria
Corticosteroid treatment of kidney disease in a patient with familial lecithin-cholesterol acyltransferase deficiency.
Proteinuria
Familial lecithin-cholesterol acyltransferase (LCAT) deficiency; a differential of proteinuria.
Proteinuria
Lecithin-cholesterol acyltransferase (LCAT) deficiency without mutations in the coding sequence: a case report and literature review.
Proteinuria
Paradoxical fall in proteinuria during pregnancy in an LCAT-deficient patient-A case report.
Proteinuria
Sex dimorphism in serum lecithin: cholesterol acyltransferase and lipoprotein lipase activities in adult sickle cell anaemia patients with proteinuria.
Proteinuria
Therapeutic management of a new case of LCAT deficiency with a multifactorial long-term approach based on high doses of angiotensin II receptor blockers (ARBs).
Proteinuria
Two different allelic mutations in the lecithin:cholesterol acyltransferase (LCAT) gene resulting in classic LCAT deficiency: LCAT (tyr83-->stop) and LCAT (tyr156-->asn).
Proteinuria
Two novel mutations of lecithin:cholesterol acyltransferase (LCAT) gene and the influence of APOE genotypes on clinical manifestations.
Proteinuria
[Corneal opacity as the leading symptom of hereditary lecithin-cholesterol acyltransferase (LCAT) deficiency. Case report and a review of the literature]
Psoriasis
Biological anti-psoriatic therapy profoundly affects high-density lipoprotein function.
Renal Insufficiency
A novel frameshift mutation of the lecithin:cholesterol acyltransferase (LCAT) gene associated with renal failure in familial LCAT deficiency.
Renal Insufficiency
A novel in vivo lecithin-cholesterol acyltransferase (LCAT)-deficient mouse expressing predominantly LpX is associated with spontaneous glomerulopathy.
Renal Insufficiency
Atorvastatin Improves Hepatic Lipid Metabolism and Protects Renal Damage in Adenine-Induced Chronic Kidney Disease in Sprague-Dawley Rats.
Renal Insufficiency
Characterization of a new LCAT mutation causing familial LCAT deficiency (FLD) and the role of APOE as a modifier gene of the FLD phenotype.
Renal Insufficiency
Familial Lecithin:cholesterol acyltransferase deficiency with renal failure in two siblings. First case report from India.
Renal Insufficiency
Lipoprotein subfractions highly associated with renal damage in familial lecithin:cholesterol acyltransferase deficiency.
Renal Insufficiency
Molecular defect in familial lecithin:cholesterol acyltransferase (LCAT) deficiency: a single nucleotide insertion in LCAT gene causes a complete deficient type of the disease.
Renal Insufficiency
Renal failure in familial lecithin-cholesterol acyltransferase deficiency.
Renal Insufficiency
Renal failure in familial lecithin: cholesterol acyltransferase deficiency.
Renal Insufficiency, Chronic
Acquired lecithin:cholesterol acyltransferase deficiency as a major factor in lowering plasma HDL levels in chronic kidney disease.
Renal Insufficiency, Chronic
Familial Lecithin Cholesterol Acyl Transferase Deficiency with Chronic Kidney Disease.
Renal Insufficiency, Chronic
Low Plasma Lecithin: Cholesterol Acyltransferase (LCAT) Concentration Predicts Chronic Kidney Disease.
Renal Insufficiency, Chronic
Novel Missense LCAT Gene Mutation Associated with an Atypical Phenotype of Familial LCAT Deficiency in Two Portuguese Brothers.
Renal Insufficiency, Chronic
[Causes and risks of hyperlipidemia during dialysis and after renal transplantation]
Sarcoidosis
A case of acquired lecithin:cholesterol acyltransferase deficiency with sarcoidosis that remitted spontaneously.
Schistosomiasis
[Plasma lecithin-cholesterol acyltransferase activity (LCAT) in late schistosomiasis and chronic liver disease]
Schistosomiasis mansoni
Alterations in the fatty acyl composition of plasma cholesteryl esters in Brazilian patients with hepatosplenic schistosomiasis mansoni.
Schistosomiasis mansoni
Effect of experimental schistosomiasis mansoni on plasma and erythrocyte lipids and on plasma lecithin: cholesterol acyltransferase in the mouse.
Schistosomiasis mansoni
Lecithin:cholesterol acyltransferase deficiency associated with hepatic schistosomiasis mansoni.
Sea-Blue Histiocyte Syndrome
Splenomegaly with sea-blue histiocytosis, dyslipidemia, and nephropathy in a patient with lecithin-cholesterol acyltransferase deficiency: a clinicopathologic correlation.
Sepsis
Alteration of Lysophosphatidylcholine-Related Metabolic Parameters in the Plasma of Mice with Experimental Sepsis.
Sepsis
Alterations in lipoprotein homeostasis during human experimental endotoxemia and clinical sepsis.
Sleep Deprivation
[Sleep deprivation effect on lecithin-cholesterol acyltransferase basal activity and on plasma levels of triglycerides and cholesterol (author's transl)]
Starvation
Effects of starvation and plasma exchange on lecithin: cholesterol acyltransferase activity and cholesterol efflux in cholesterol-fed pigs.
sterol o-acyltransferase deficiency
[Familial alpha lipoprotein deficiency. Tangier disease, familial hypoalphalipoproteinemia and familial deficiency of lecithin cholesterol acyltransferase deficiency]
Tangier Disease
Apoprotein A-I and lecithin: cholesterol acyltransferase in a patient with Tangier disease.
Tangier Disease
Cholesterol esterification by lecithin-cholesterol acyltransferase in A-I-free plasma.
Tangier Disease
Cholesteryl ester transfer activity in plasma of patients with familial high-density lipoprotein deficiency.
Tangier Disease
Clinical variant of Tangier disease in Japan: mutation of the ABCA1 gene in hypoalphalipoproteinemia with corneal lipidosis.
Tangier Disease
Different substrate specificities of plasma lecithin: cholesterol acyl transferase in fish eye disease and Tangier disease.
Tangier Disease
Familial splenomegaly: macrophage hypercatabolism of lipoproteins associated with apolipoprotein E mutation [apolipoprotein E (delta149 Leu)].
Tangier Disease
Generation of pre-beta 1-HDL and conversion into alpha-HDL. Evidence for disturbed HDL conversion in Tangier disease.
Tangier Disease
Isolated low HDL-cholesterol as an important risk factor for coronary heart disease.
Tangier Disease
Lecithin:cholesterol acyltransferase in familial HDL deficiency (Tangier disease).
Tangier Disease
Reverse cholesterol transport in plasma of patients with different forms of familial HDL deficiency.
Tangier Disease
The role of high density lipoproteins in lecithin:cholesterol acyltransferase activity: perspectives from Tangier disease.
Tangier Disease
[Familial alpha lipoprotein deficiency. Tangier disease, familial hypoalphalipoproteinemia and familial deficiency of lecithin cholesterol acyltransferase deficiency]
Thrombotic Microangiopathies
Histiocytic and Nonhistiocytic Glomerular Lesions: Foam Cells and Their Mimickers.
triacylglycerol lipase deficiency
Alpha-lecithin:cholesterol acyltransferase deficiency. Lack of both phospholipase A2 and acyltransferase activities characteristic of high density lipoprotein lecithin:cholesterol acyltransferase in fish eye disease.
triacylglycerol lipase deficiency
Apolipoprotein AIMilano. Partial lecithin:cholesterol acyltransferase deficiency due to low levels of a functional enzyme.
triacylglycerol lipase deficiency
Causes of dysregulation of lipid metabolism in chronic renal failure.
triacylglycerol lipase deficiency
Lipoprotein abnormalities associated with lipopolysaccharide-induced lecithin: cholesterol acyltransferase and lipase deficiency.
triacylglycerol lipase deficiency
[Familial alpha lipoprotein deficiency. Tangier disease, familial hypoalphalipoproteinemia and familial deficiency of lecithin cholesterol acyltransferase deficiency]
Vascular Diseases
Lecithin: cholesterol acyltransferase (LCAT) deficiency and risk of vascular disease: 25 year follow-up.
Vitamin E Deficiency
Depression of lecithin-cholesterol acyltransferase esterification in vitamin E-deficient monkeys.
Vitamin E Deficiency
Studies of serum lecithin-cholesterol acyl transferase activity in rat: effect of vitamin E deficiency, oxidized dietary fat, or intravenous administration of ozonides or hydroperoxides.
Xanthomatosis, Cerebrotendinous
Increased concentrations of cholestanol and apolipoprotein B in the cerebrospinal fluid of patients with cerebrotendinous xanthomatosis. Effect of chenodeoxycholic acid.
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