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Disease on EC 1.13.11.18 - persulfide dioxygenase

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DISEASE
TITLE OF PUBLICATION
LINK TO PUBMED
Acquired Immunodeficiency Syndrome
Intergroup contact, social dominance, and environmental concern: A test of the cognitive-liberalization hypothesis.
Adenomatous Polyposis Coli
ETHE1 overexpression promotes SIRT1 and PGC1? mediated aerobic glycolysis, oxidative phosphorylation, mitochondrial biogenesis and colorectal cancer.
Anemia, Hypochromic
The mitochondrial sulfur dioxygenase ETHE1 is required for amino acid catabolism during carbohydrate starvation and embryo development in Arabidopsis thaliana.
Brain Diseases
Acute and Chronic Management in an Atypical Case of Ethylmalonic Encephalopathy.
Acute Strokelike Presentation and Long-term Evolution of Diffusion Restriction Pattern in Ethylmalonic Encephalopathy.
Arabidopsis ETHE1 Encodes a Sulfur Dioxygenase That Is Essential for Embryo and Endosperm Development.
Characterization of patient mutations in human persulfide dioxygenase (ETHE1) involved in H2S catabolism.
Chronic Exposure to Sulfide causes Accelerated Degradation of Cytochrome c oxidase in Ethylmalonic Encephalopathy.
Combined treatment with oral metronidazole and N-acetylcysteine is effective in ethylmalonic encephalopathy.
Compromised therapeutic value of pediatric liver transplantation in ethylmalonic encephalopathy: A case report.
Crystal structure of human persulfide dioxygenase: structural basis of ethylmalonic encephalopathy.
Deficiency of the mitochondrial sulfide regulator ETHE1 disturbs cell growth, glutathione level and causes proteome alterations outside mitochondria.
Distribution, diversity, and activities of sulfur dioxygenases in heterotrophic bacteria.
ETHE1 mutations are specific to ethylmalonic encephalopathy.
ETHE1 overexpression promotes SIRT1 and PGC1? mediated aerobic glycolysis, oxidative phosphorylation, mitochondrial biogenesis and colorectal cancer.
Ethylmalonic encephalopathy associated with crescentic glomerulonephritis.
Ethylmalonic encephalopathy ETHE1 p. D165H mutation alters the mitochondrial function in human skeletal muscle proteome.
Ethylmalonic encephalopathy ETHE1 R163W/R163Q mutations alter protein stability and redox properties of the iron centre.
Ethylmalonic encephalopathy is caused by mutations in ETHE1, a gene encoding a mitochondrial matrix protein.
Ethylmalonic encephalopathy: Clinical course and therapy response in an uncommon mild case with a severe ETHE1 mutation.
Expression of abiotic stress inducible ETHE1-like protein from rice is higher in roots and is regulated by calcium.
Expression of abiotic stress inducible ETHE1?like protein from rice is higher in roots and is regulated by calcium
Identification of a novel homozygous nonsense variant in a Chinese patient with ethylmalonic encephalopathy and a genotype-phenotype spectrum review.
Identification of new mutations in the ETHE1 gene in a cohort of 14 patients presenting with ethylmalonic encephalopathy.
Improved clinical outcome following liver transplant in patients with ethylmalonic encephalopathy.
Loss of ETHE1, a mitochondrial dioxygenase, causes fatal sulfide toxicity in ethylmalonic encephalopathy.
Mitochondrial diseases caused by toxic compound accumulation: from etiopathology to therapeutic approaches.
Mitochondrial Dysfunction and Redox Homeostasis Impairment as Pathomechanisms of Brain Damage in Ethylmalonic Encephalopathy: Insights from Animal and Human Studies.
Multiple sources of metabolic disturbance in ETHE1-related ethylmalonic encephalopathy.
Novel Compound Heterozygous Variants of ETHE1 Causing Ethylmalonic Encephalopathy in a Chinese Patient: A Case Report.
Novel ETHE1 mutation in a carrier couple having prior offspring affected with ethylmalonic encephalopathy: Genetic analysis, clinical management and reproductive outcome.
Protein polysulfidation-dependent persulfide dioxygenase activity of ethylmalonic encephalopathy protein 1.
Proteomics Reveals that Redox Regulation Is Disrupted in Patients with Ethylmalonic Encephalopathy.
Quantitative proteomics suggests metabolic reprogramming during ETHE1 deficiency.
Response to medical and a novel dietary treatment in newborn screen identified patients with ethylmalonic encephalopathy.
Severe early onset ethylmalonic encephalopathy with West syndrome.
Spectroscopic studies on Arabidopsis ETHE1, a glyoxalase II-like protein.
Staphylococcus aureus CstB Is a Novel Multidomain Persulfide Dioxygenase-Sulfurtransferase Involved in Hydrogen Sulfide Detoxification.
Stress response of OsETHE1 is altered in response to light and dark conditions.
Structure of an ETHE1-like protein from Arabidopsis thaliana.
Sulfide detoxification in plant mitochondria.
Untargeted Metabolomics Analysis Reveals a Link between ETHE1-Mediated Disruptive Redox State and Altered Metabolic Regulation.
[Clinical and genetic analysis of a case with atypical ethyl malonate encephalopathy].
Carcinogenesis
ETHE1 overexpression promotes SIRT1 and PGC1? mediated aerobic glycolysis, oxidative phosphorylation, mitochondrial biogenesis and colorectal cancer.
Colorectal Neoplasms
ETHE1 overexpression promotes SIRT1 and PGC1? mediated aerobic glycolysis, oxidative phosphorylation, mitochondrial biogenesis and colorectal cancer.
Systems Biomedicine of Primary and Metastatic Colorectal Cancer Reveals Potential Therapeutic Targets.
Congenital Abnormalities
Total hip arthroplasty requiring subtrochanteric osteotomy for developmental hip dysplasia 5- to 14-year results.
COVID-19
U.S. public support for COVID-19 vaccine donation to low- and middle-income countries during the COVID-19 pandemic.
Craniocerebral Trauma
Increased Risks of Suicide Attempt and Suicidal Drug Overdose Following Admission for Head Injury in Patients with Depression.
Increasing Risks of Suicide Attempt and Suicidal Drug Overdose After Head Trauma in Patients With Sleep-Disordered Breathing: A Population-Based Study.
Craniosynostoses
Piezosurgical Suturectomy and Sutural Distraction Osteogenesis for the Treatment of Unilateral Coronal Synostosis.
Cytochrome-c Oxidase Deficiency
Chronic Exposure to Sulfide causes Accelerated Degradation of Cytochrome c oxidase in Ethylmalonic Encephalopathy.
Diabetic Nephropathies
Evaluating Pharmacological Effects of Two Major Components of Shuangdan Oral Liquid: Role of Danshensu and Paeonol in Diabetic Nephropathy Rat.
Enteritis
[Epidemiological impact of RV gastroenteritis in the Abruzzo Region: SDO analysis]
Epilepsy
Differences in Incidence and Risks of Suicide Attempt and Suicidal Drug Overdose between Patients with Epilepsy with and without Comorbid Depression.
Gastroenteritis
[Epidemiological impact of RV gastroenteritis in the Abruzzo Region: SDO analysis]
Hyperlipidemias
Metabolomics analysis of the therapeutic mechanism of Semen Descurainiae Oil on hyperlipidemia rats using 1 H-NMR and LC-MS.
Hypospadias
Hypospadias prevalence in the Emilia Romagna Region registry: Increasing or methodology?
Infections
The role of short-chain dehydrogenase/oxidoreductase, induced by salt stress, on host interaction of B. pseudomallei.
Melanoma
Second Diagnostic Opinion by Experienced Dermatopathologists in the Setting of a Referral Regional Melanoma Unit Significantly Improves the Clinical Management of Patients With Cutaneous Melanoma.
Melioidosis
Altered proteome of a Burkholderia pseudomallei mutant defective in short-chain dehydrogenase affects cell adhesion, biofilm formation and heat stress tolerance.
Metabolic Syndrome
Lipogenesis is decreased by grape seed proanthocyanidins according to liver proteomics of rats fed a high fat diet.
Mitochondrial Diseases
Acute Strokelike Presentation and Long-term Evolution of Diffusion Restriction Pattern in Ethylmalonic Encephalopathy.
Improved clinical outcome following liver transplant in patients with ethylmalonic encephalopathy.
Mitochondrial diseases caused by toxic compound accumulation: from etiopathology to therapeutic approaches.
Neoplasms
[Extending traceability of malignant testicular tumours using hospital discharge records: an experience in Veneto Region (Northern Italy)].
Neurodegenerative Diseases
Identification of a novel homozygous nonsense variant in a Chinese patient with ethylmalonic encephalopathy and a genotype-phenotype spectrum review.
Response to medical and a novel dietary treatment in newborn screen identified patients with ethylmalonic encephalopathy.
Obesity
Obesity discrimination: the role of physical appearance, personal ideology, and anti-fat prejudice.
Ovarian Neoplasms
Salpingectomy for the Risk Reduction of Ovarian Cancer: Is It Time for a Salpingectomy-alone Approach?
Overweight
Feminist identification, social dominance orientation, and weight bias in men.
Paraparesis, Spastic
Ethylmalonic encephalopathy: Clinical course and therapy response in an uncommon mild case with a severe ETHE1 mutation.
Parkinson Disease
Spatiotemporal characteristics of postsaccadic dynamic overshoot in young and elderly subjects.
persulfide dioxygenase deficiency
Deficiency of the mitochondrial sulfide regulator ETHE1 disturbs cell growth, glutathione level and causes proteome alterations outside mitochondria.
ETHE1 and MOCS1 deficiencies: Disruption of mitochondrial bioenergetics, dynamics, redox homeostasis and endoplasmic reticulum-mitochondria crosstalk in patient fibroblasts.
Evidence that thiol group modification and reactive oxygen species are involved in hydrogen sulfide-induced mitochondrial permeability transition pore opening in rat cerebellum.
Evidence that Thiosulfate Inhibits Creatine Kinase Activity in Rat Striatum via Thiol Group Oxidation.
Morphologic evidence of diffuse vascular damage in human and in the experimental model of ethylmalonic encephalopathy.
Quantitative proteomics suggests metabolic reprogramming during ETHE1 deficiency.
The Role of Persulfide Metabolism During Arabidopsis Seed Development Under Light and Dark Conditions.
Untargeted Metabolomics Analysis Reveals a Link between ETHE1-Mediated Disruptive Redox State and Altered Metabolic Regulation.
Pulmonary Disease, Chronic Obstructive
Suicide Attempt and Suicidal Drug Overdose in Chronic Obstructive Pulmonary Disease Patients With or Without Depression.
Purpura
Ethylmalonic encephalopathy associated with crescentic glomerulonephritis.
Starvation
Stress response of OsETHE1 is altered in response to light and dark conditions.
The mitochondrial sulfur dioxygenase ETHE1 is required for amino acid catabolism during carbohydrate starvation and embryo development in Arabidopsis thaliana.
The Role of Persulfide Metabolism During Arabidopsis Seed Development Under Light and Dark Conditions.
Stroke
Suicidal drug overdose following stroke in elderly patients: a retrospective population-based cohort study.
Synostosis
Piezosurgical Suturectomy and Sutural Distraction Osteogenesis for the Treatment of Unilateral Coronal Synostosis.
Synovitis
Identification of pathways and genes associated with synovitis in osteoarthritis using bioinformatics analyses.
Testicular Neoplasms
[Extending traceability of malignant testicular tumours using hospital discharge records: an experience in Veneto Region (Northern Italy)].