methionine has been researched along with Electron Transport Chain Deficiencies, Mitochondrial in 11 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 5 (45.45) | 29.6817 |
| 2010's | 4 (36.36) | 24.3611 |
| 2020's | 2 (18.18) | 2.80 |
| Authors | Studies |
|---|---|
| Chen, FF; Guan, XL; Ni, L; Wu, PF | 1 |
| F C Lopes, A | 1 |
| Alberti, JM; Baloh, RH; Biris, N; Dorn, GW; Franco, A; Gavathiotis, E; Janetka, JW; Kitsis, RN; Knight, WC; Krezel, AM; Mochly-Rosen, D; Rocha, AG; Rumsey, JM; Townsend, RR; Zacharioudakis, E | 1 |
| Afroze, B; Ali, ZZ; Fatimah, M; Jafri, L; Jamil, A; Khan, AH; Majid, H; Yusufzai, N | 1 |
| Banasch, M; Ellrichmann, M; Emminghaus, R; Goetze, O; Schmidt, WE | 1 |
| Banasch, M; Brockmeyer, NH; Goetze, O; Knyhala, K; Kollar, S; Potthoff, A; Schlottmann, R; Schmidt, WE; Serova, K | 1 |
| Bellon, A; Frieling, H; Jay, TM; Krebs, MO; Mainguy, G | 1 |
| Mudd, SH | 1 |
| Allen, RH; Luka, Z; Mudd, SH; Schroer, R; Stabler, SP; Wagner, C; Wang, J; Wong, LJ; Wood, T | 1 |
| Barve, S; Cave, M; Deaciuc, I; Joshi-Barve, S; McClain, C; Mendez, C; Song, Z | 1 |
| Hayakawa, C; Kanazawa, N; Miyamoto, T; Tsujino, S | 1 |
3 review(s) available for methionine and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
Mitochondrial metabolism and DNA methylation: a review of the interaction between two genomes.
Topics: Animals; Carbon; Cell Nucleus; Citric Acid Cycle; CpG Islands; DNA Methylation; DNA, Mitochondrial; Epigenesis, Genetic; Epigenomics; Genome; Haploidy; Humans; Methionine; Mitochondria; Mitochondrial Diseases; Models, Animal; Mutation; Prevalence | 2020 |
Hypermethioninemias of genetic and non-genetic origin: A review.
Topics: Adenosylhomocysteinase; Amino Acid Metabolism, Inborn Errors; Calcium-Binding Proteins; cis-trans-Isomerases; Cystathionine beta-Synthase; Diagnosis, Differential; Female; Glycine N-Methyltransferase; Humans; Infant, Newborn; Liver Diseases; Methionine; Methionine Adenosyltransferase; Mitochondrial Diseases; Neonatal Screening; Organic Anion Transporters; Tyrosinemias | 2011 |
Nonalcoholic fatty liver disease: predisposing factors and the role of nutrition.
Topics: Betaine; Cytokines; Dietary Supplements; Environmental Exposure; Fatty Liver; Female; Humans; Insulin Resistance; Life Style; Liver; Liver Cirrhosis; Metabolic Syndrome; Methionine; Middle Aged; Mitochondrial Diseases; Oxidative Stress; S-Adenosylmethionine; United States; Vitamin E; Xenobiotics; Zinc | 2007 |
8 other study(ies) available for methionine and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
S-methyl-L-cysteine Protects against Antimycin A-induced Mitochondrial Dysfunction in Neural Cells via Mimicking Endogenous Methionine-centered Redox Cycle.
Topics: Animals; Antimycin A; Antioxidants; Cell Line, Tumor; Cysteine; Humans; Membrane Potential, Mitochondrial; Methionine; Methionine Sulfoxide Reductases; Mitochondria; Mitochondrial Diseases; Neurons; Oxidation-Reduction; Oxidative Stress; PC12 Cells; Rats | 2020 |
MFN2 agonists reverse mitochondrial defects in preclinical models of Charcot-Marie-Tooth disease type 2A.
Topics: Amino Acid Substitution; Animals; Arginine; Axons; Charcot-Marie-Tooth Disease; Disease Models, Animal; Drug Design; Glutamine; GTP Phosphohydrolases; Humans; Methionine; Mice; Mice, Inbred C57BL; Mitochondria; Mitochondrial Diseases; Mitochondrial Proteins; Oligopeptides; Phosphorylation; Protein Kinases; Sciatic Nerve; Small Molecule Libraries; Threonine | 2018 |
Diagnostic dilemma of patients with methylmalonic aciduria: Experience from a tertiary care centre in Pakistan.
Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Child, Preschool; Citrates; Cross-Sectional Studies; Female; Glycine; Humans; Infant; Lactic Acid; Male; Methionine; Mitochondrial Diseases; Pakistan; Tertiary Care Centers; Urinalysis; Valerates; Vitamin B 12 Deficiency | 2018 |
Longitudinal effects of hepatitis C virus treatment on hepatic mitochondrial dysfunction assessed by C-methionine breath test.
Topics: Adult; Antiviral Agents; Breath Tests; Case-Control Studies; Female; Genotype; Hepatitis C, Chronic; Humans; Interferon alpha-2; Interferon-alpha; Liver Function Tests; Longitudinal Studies; Male; Methionine; Middle Aged; Mitochondria, Liver; Mitochondrial Diseases; Oxidative Stress; Polyethylene Glycols; Predictive Value of Tests; Recombinant Proteins; Ribavirin; RNA, Viral; Treatment Outcome; Viral Load | 2008 |
Disease- and treatment-related predictors of hepatic mitochondrial dysfunction in chronic HIV infection assessed by non-invasive (13)C-methionine breath test diagnostic.
Topics: Adult; Anti-Retroviral Agents; Breath Tests; Carbon Isotopes; Chronic Disease; Female; HIV Infections; Humans; Male; Methionine; Middle Aged; Mitochondria, Liver; Mitochondrial Diseases; Predictive Value of Tests | 2008 |
One-carbon metabolism and schizophrenia: current challenges and future directions.
Topics: Carbon; DNA Methylation; Environment; Epigenesis, Genetic; Folic Acid Deficiency; Genetic Predisposition to Disease; Homocysteine; Humans; Metabolic Networks and Pathways; Methionine; Mitochondrial Diseases; Receptors, Glutamate; Schizophrenia; Time Factors | 2009 |
Two patients with hepatic mtDNA depletion syndromes and marked elevations of S-adenosylmethionine and methionine.
Topics: Adolescent; Base Sequence; DNA, Mitochondrial; Exons; Female; Glycine N-Methyltransferase; Humans; Infant; Liver; Male; Membrane Proteins; Methionine; Mitochondrial Diseases; Mitochondrial Proteins; Molecular Sequence Data; Mutation; S-Adenosylmethionine; Sequence Deletion | 2012 |
A novel mutation, P126R, in a Japanese patient with HHH syndrome.
Topics: Adolescent; Ammonia; Base Sequence; Brain Diseases; Carrier Proteins; Cysts; DNA Primers; Exons; Gene Expression; Humans; Magnetic Resonance Imaging; Male; Metabolism, Inborn Errors; Methionine; Mitochondrial Diseases; Molecular Sequence Data; Ornithine; Point Mutation; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Septum Pellucidum; Syndrome; Tomography, X-Ray Computed | 2002 |