tryptophan has been researched along with Electron Transport Chain Deficiencies, Mitochondrial in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (33.33) | 29.6817 |
| 2010's | 3 (50.00) | 24.3611 |
| 2020's | 1 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Polyák, H; Spekker, E; Szabó, Á; Tanaka, M; Tóth, F; Vécsei, L | 1 |
| Adanyeguh, I; Collins, B; Durr, A; Evans, RM; Fan, W; Ichou, F; Kinoshita, C; La Spada, AR; Mochel, F; Morrison, RS; Muotri, AR; Niu, C; Sopher, BL; Stoyas, CA; Switonski, PM; Wall, CE; Ward, JM | 1 |
| Ben-Sira, L; Blumkin, L; Edvardson, S; Henneke, M; Lerman-Sagie, T; Leshinsky-Silver, E; Lev, D; Nishri, D | 1 |
| Fülöp, F; Klivényi, P; Toldi, J; Vámos, E; Vécsei, L; Zádori, D | 1 |
| Karlsson, A; Larsson, NG; Lesko, N; Naess, K; Nennesmo, I; Solaroli, N; von Döbeln, U; Wibom, R | 1 |
| Chan, SS; Copeland, WC; Longley, MJ | 1 |
2 review(s) available for tryptophan and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
Mitochondrial Impairment: A Common Motif in Neuropsychiatric Presentation? The Link to the Tryptophan-Kynurenine Metabolic System.
Topics: Animals; DNA, Mitochondrial; Humans; Kynurenine; Mitochondria; Mitochondrial Diseases; Tryptophan | 2022 |
Kynurenines in chronic neurodegenerative disorders: future therapeutic strategies.
Topics: Animals; Brain; Glutamic Acid; Humans; Kynurenic Acid; Mitochondrial Diseases; NAD; Neurodegenerative Diseases; Neuroprotective Agents; Phosphatidylinositol 3-Kinases; Phosphoinositide-3 Kinase Inhibitors; Quinolinic Acid; Tryptophan | 2009 |
4 other study(ies) available for tryptophan and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
Metabolic and Organelle Morphology Defects in Mice and Human Patients Define Spinocerebellar Ataxia Type 7 as a Mitochondrial Disease.
Topics: Adipose Tissue; Animals; Ataxin-7; Blood Glucose; Energy Metabolism; Humans; Kynurenine; Metabolomics; Mice; Mitochondria; Mitochondrial Diseases; NAD; Neural Stem Cells; Organelles; Peptides; Phenotype; Purkinje Cells; Reproducibility of Results; Spinocerebellar Ataxias; Trinucleotide Repeat Expansion; Tryptophan | 2019 |
Diagnosis by whole exome sequencing of atypical infantile onset Alexander disease masquerading as a mitochondrial disorder.
Topics: Alexander Disease; Arginine; Child, Preschool; Exome; Female; Frontal Lobe; Glial Fibrillary Acidic Protein; High-Throughput Nucleotide Sequencing; Humans; Magnetic Resonance Imaging; Mitochondrial Diseases; Mutation; Tryptophan; White Matter | 2014 |
Two novel mutations in thymidine kinase-2 cause early onset fatal encephalomyopathy and severe mtDNA depletion.
Topics: Adenosine Triphosphate; Arginine; Child; Child, Preschool; DNA Mutational Analysis; DNA, Mitochondrial; Female; Genetic Predisposition to Disease; Humans; Infant; Infant, Newborn; Male; Mitochondria; Mitochondria, Muscle; Mitochondrial Diseases; Mitochondrial Encephalomyopathies; Muscle, Skeletal; Mutagenesis, Site-Directed; Mutation; Thymidine Kinase; Tryptophan | 2010 |
Modulation of the W748S mutation in DNA polymerase gamma by the E1143G polymorphismin mitochondrial disorders.
Topics: Amino Acid Sequence; Amino Acid Substitution; Catalytic Domain; DNA; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Enzyme Stability; Glutamic Acid; Glycine; Humans; Mitochondrial Diseases; Models, Molecular; Molecular Sequence Data; Mutation; Nucleotides; Polymorphism, Genetic; Protein Conformation; Serine; Tryptophan | 2006 |