tyrosine has been researched along with Electron Transport Chain Deficiencies, Mitochondrial in 18 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 10 (55.56) | 29.6817 |
| 2010's | 8 (44.44) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chowdhury, N; Delatorre, R; Frye, RE; James, SJ; Melnyk, S; Slattery, J; Taylor, H | 1 |
| Cannon, JR; Greenamyre, JT; Tapias, V | 1 |
| Coats, BS; Langaee, T; McDonough, CW; Shroads, AL; Stacpoole, PW | 1 |
| Donner, JR; Holmbeck, MA; Rand, DM; Villa-Cuesta, E | 1 |
| Parikh, JG; Rao, NA; Saraswathy, S | 1 |
| Adochio, R; Draznin, B; Kim, T; Wayne Leitner, J | 1 |
| Chinault, AC; Dimmock, D; Huang, WC; Hwu, WL; Lee, NC; Tang, LY; Wong, LJ | 1 |
| Hargreaves, I; Kyprianou, N; Lee, P; Murphy, E | 1 |
| Ballinger, CA; Ballinger, SW; Chuang, GC; Krzywanski, DM; Pompilius, M; Postlethwait, EM; Westbrook, DG; White, CR; Yang, Z | 1 |
| Folbergrová, J; Haugvicová, R; Houstek, J; Jesina, P; Lisý, V | 1 |
| Arcaro, G; Chiamulera, C; Degan, M; Di Chio, M; Grigoli, L; Guglielmi, V; Klouckova, I; Lechi, A; Lovato, L; Marini, M; Mechref, Y; Meneguzzi, A; Minuz, P; Novotny, MV; Tedesco, V; Tomelleri, G; Tonin, P; Vattemi, G | 1 |
| Cooley, JW; Daldal, F; Forquer, I; Kramer, DM; Lanciano, P; Lee, DW; Selamoglu, N | 1 |
| de Oliveira, MR; Lorenzi, R; Moreira, JC; Morrone, M; Schnorr, CE | 1 |
| Hawkins, EP; Liu, LL; Scaglia, F; Vladutiu, GD; Vogel, H; Wong, LJ | 1 |
| Derenko, MV; Grzybowski, T; Malyarchuk, BA; Miścicka-Sliwka, D; Stopińska, K | 1 |
| Hall, ED; Mbye, LH; Singh, IN; Springer, JE; Sullivan, PG | 1 |
| Abdul, HM; Batinic-Haberle, I; Butterfield, DA; Chen, Y; Doubinskaia, I; Ittarat, W; Sompol, P; St Clair, DK; Tangpong, J | 1 |
| Albers, DS; Beal, MF; Gibson, GE; Lindsay, JG; Park, LC; Xu, H | 1 |
1 trial(s) available for tyrosine and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
Haplotype variations in glutathione transferase zeta 1 influence the kinetics and dynamics of chronic dichloroacetate in children.
Topics: Acetone; Adolescent; Adult; Aminolevulinic Acid; Child; Child, Preschool; Dichloroacetic Acid; Double-Blind Method; Female; Genetic Diseases, Inborn; Glutathione Transferase; Haplotypes; Humans; Infant; Kinetics; Male; Maleates; Mitochondrial Diseases; Polymorphism, Single Nucleotide; Tyrosine; Young Adult | 2015 |
17 other study(ies) available for tyrosine and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
Redox metabolism abnormalities in autistic children associated with mitochondrial disease.
Topics: Age Factors; Biomarkers; Child; Child Development Disorders, Pervasive; Female; Glutathione; Humans; Language Development; Male; Mitochondrial Diseases; Neuropsychological Tests; Oxidation-Reduction; Oxidative Stress; Tyrosine | 2013 |
Pomegranate juice exacerbates oxidative stress and nigrostriatal degeneration in Parkinson's disease.
Topics: Animals; Caspase 3; Disease Models, Animal; Dopaminergic Neurons; Inflammation; Lythraceae; Male; Mitochondrial Diseases; Nitric Oxide Synthase Type II; Oxidative Stress; Parkinson Disease; Rats; Rats, Inbred Lew; Rotenone; Substantia Nigra; Tyrosine | 2014 |
A Drosophila model for mito-nuclear diseases generated by an incompatible interaction between tRNA and tRNA synthetase.
Topics: Amino Acyl-tRNA Synthetases; Animal Structures; Animals; Animals, Genetically Modified; Cell Nucleus; Cell Respiration; Disease Models, Animal; Drosophila melanogaster; Epistasis, Genetic; Flight, Animal; Genotype; Mitochondria, Muscle; Mitochondrial Diseases; Motor Activity; Muscles; Oxidative Phosphorylation; Peptide Chain Initiation, Translational; RNA, Transfer; Tyrosine | 2015 |
Photoreceptor oxidative damage in sympathetic ophthalmia.
Topics: Acrolein; Adult; Aged; Apoptosis; Biomarkers; Cytochromes c; Fluorescent Antibody Technique, Indirect; Humans; In Situ Nick-End Labeling; Middle Aged; Mitochondrial Diseases; Nitric Oxide Synthase Type II; Ophthalmia, Sympathetic; Oxidative Stress; Photoreceptor Cells, Vertebrate; Receptors, Tumor Necrosis Factor, Type I; Tumor Necrosis Factor-alpha; Tyrosine | 2008 |
Knockdown of JNK rescues 3T3-L1 adipocytes from insulin resistance induced by mitochondrial dysfunction.
Topics: 3T3-L1 Cells; Adipocytes; Animals; Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone; Deoxyglucose; Gene Knockdown Techniques; Insulin; Insulin Receptor Substrate Proteins; Insulin Resistance; Mice; Mitochondrial Diseases; Mitogen-Activated Protein Kinase 8; Phosphatidylinositol 3-Kinases; Phosphorylation; Serine; Tyrosine | 2009 |
Simultaneous detection of mitochondrial DNA depletion and single-exon deletion in the deoxyguanosine gene using array-based comparative genomic hybridisation.
Topics: Alanine; Base Sequence; Deoxyguanine Nucleotides; DNA Mutational Analysis; DNA, Mitochondrial; Exons; Gene Deletion; Genetic Carrier Screening; Humans; Infant; Infant, Newborn; Liver Failure; Male; Mitochondrial Diseases; Molecular Sequence Data; Mutation, Missense; Oligonucleotide Array Sequence Analysis; Tandem Mass Spectrometry; Treatment Outcome; Tyrosine | 2009 |
Assessment of mitochondrial respiratory chain function in hyperphenylalaninaemia.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Cell Line, Tumor; Cells, Cultured; Culture Media; Electron Transport; Female; Humans; Lactic Acid; Male; Middle Aged; Mitochondrial Diseases; Phenylalanine; Phenylketonurias; Pyruvic Acid; Tremor; Tyrosine; Ubiquinone; Young Adult | 2009 |
Pulmonary ozone exposure induces vascular dysfunction, mitochondrial damage, and atherogenesis.
Topics: Air Pollutants; Animals; Aorta; Atherosclerosis; Blood Pressure; DNA Damage; DNA, Mitochondrial; Heart Rate; Lung Diseases; Macaca mulatta; Male; Mice; Mice, Inbred C57BL; Mitochondria; Mitochondrial Diseases; Nitrates; Nitric Oxide; Nitric Oxide Synthase Type III; Nitrites; Oxidants; Oxidative Stress; Ozone; Superoxide Dismutase; Tyrosine | 2009 |
Sustained deficiency of mitochondrial complex I activity during long periods of survival after seizures induced in immature rats by homocysteic acid.
Topics: Aldehydes; Animals; Animals, Newborn; Cerebral Cortex; Convulsants; Disease Models, Animal; Down-Regulation; Electron Transport Complex I; Energy Metabolism; Epilepsy; Excitatory Amino Acid Agonists; Free Radical Scavengers; Homocysteine; Male; Metabolic Networks and Pathways; Mitochondria; Mitochondrial Diseases; Oxidative Stress; Rats; Rats, Wistar; Seizures; Survival Rate; Time Factors; Tyrosine | 2010 |
Increased protein nitration in mitochondrial diseases: evidence for vessel wall involvement.
Topics: Adolescent; Adult; Aged; Base Sequence; Brachial Artery; Case-Control Studies; Deafness; Diabetes Mellitus, Type 2; Endothelium, Vascular; Female; Femoral Artery; Humans; Kearns-Sayre Syndrome; Male; MELAS Syndrome; MERRF Syndrome; Middle Aged; Mitochondrial Diseases; Muscle, Skeletal; Muscle, Smooth, Vascular; Nitric Oxide Synthase Type I; Nitric Oxide Synthase Type III; Point Mutation; Sequence Deletion; Tyrosine; Vasodilation | 2011 |
Loss of a conserved tyrosine residue of cytochrome b induces reactive oxygen species production by cytochrome bc1.
Topics: Amino Acid Substitution; Cytochromes b; Electron Transport Complex III; Escherichia coli; Escherichia coli Proteins; Humans; Mitochondrial Diseases; Mutation, Missense; Plasmodium; Rhodobacter capsulatus; Tyrosine | 2011 |
Increased 3-nitrotyrosine levels in mitochondrial membranes and impaired respiratory chain activity in brain regions of adult female rats submitted to daily vitamin A supplementation for 2 months.
Topics: Amyloid beta-Peptides; Animals; Antioxidants; Brain Chemistry; Electron Transport; Enzyme-Linked Immunosorbent Assay; Estrous Cycle; Female; Glycation End Products, Advanced; Mitochondrial Diseases; Mitochondrial Membranes; Monoamine Oxidase; Oxidative Stress; Rats; Rats, Wistar; Receptors, Dopamine D2; Succinate Dehydrogenase; Superoxide Dismutase; Synucleins; Thiobarbituric Acid Reactive Substances; Tumor Necrosis Factor-alpha; Tyrosine; Ubiquinone; Vitamin A; Vitamins | 2011 |
Novel homoplasmic mutation in the mitochondrial tRNATyr gene associated with atypical mitochondrial cytopathy presenting with focal segmental glomerulosclerosis.
Topics: Abnormalities, Multiple; Base Sequence; Biopsy; Child; Child, Preschool; Chromatography, High Pressure Liquid; Coenzymes; DNA, Mitochondrial; Female; Glomerulosclerosis, Focal Segmental; Humans; Immunohistochemistry; Kidney; Microscopy, Electron; Mitochondrial Diseases; Molecular Sequence Data; Muscle, Skeletal; Mutation; RNA, Transfer; Sequence Alignment; Sequence Analysis, DNA; Tyrosine; Ubiquinone | 2003 |
Optimization of the Y831C mutation detection in human DNA polymerase gamma by allelic discrimination assay.
Topics: Cysteine; DNA Polymerase gamma; DNA-Directed DNA Polymerase; DNA, Mitochondrial; Gene Frequency; Genetic Techniques; Humans; Mitochondrial Diseases; Parkinson Disease; Peripheral Nervous System Diseases; Point Mutation; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Tyrosine | 2006 |
Attenuation of acute mitochondrial dysfunction after traumatic brain injury in mice by NIM811, a non-immunosuppressive cyclosporin A analog.
Topics: Acute Disease; Aldehydes; Animals; Biomarkers; Brain Injuries; Cyclosporine; Dose-Response Relationship, Drug; Immunoblotting; Lipid Peroxidation; Male; Mice; Mitochondrial Diseases; Oxidative Stress; Oxygen Consumption; Structure-Activity Relationship; Tyrosine | 2008 |
A neuronal model of Alzheimer's disease: an insight into the mechanisms of oxidative stress-mediated mitochondrial injury.
Topics: Aldehydes; Alzheimer Disease; Amyloid beta-Protein Precursor; Animals; Animals, Newborn; Brain; Cell Respiration; Cells, Cultured; Disease Models, Animal; Humans; Membrane Potential, Mitochondrial; Metalloporphyrins; Mice; Mice, Transgenic; Mitochondria; Mitochondrial Diseases; Mutation; Neurons; Oxidative Stress; Presenilin-1; Protein Carbonylation; Superoxide Dismutase; Superoxide Dismutase-1; Tyrosine | 2008 |
Mitochondrial impairment in the cerebellum of the patients with progressive supranuclear palsy.
Topics: Aconitate Hydratase; Animals; Brain Diseases, Metabolic; Cerebellum; Down-Regulation; Energy Metabolism; Glutamate Dehydrogenase; Humans; Immunoblotting; Ketoglutarate Dehydrogenase Complex; Mice; Mitochondria; Mitochondrial Diseases; Nitric Oxide; Oxidative Stress; Subcellular Fractions; Supranuclear Palsy, Progressive; Tyrosine | 2001 |