tyrosine has been researched along with Muscle Disorders in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (28.57) | 18.7374 |
1990's | 1 (14.29) | 18.2507 |
2000's | 1 (14.29) | 29.6817 |
2010's | 2 (28.57) | 24.3611 |
2020's | 1 (14.29) | 2.80 |
Authors | Studies |
---|---|
Chen, T; Friederich, MW; Knight, KM; Kripps, KA; Larson, AA; Mirsky, DM; Tanji, K; Van Hove, JLK; Wang, Y; Wong, LJ | 1 |
Alexander, MS; Kang, PB; Mitsuhashi, H; Mitsuhashi, S; Sugimoto, H | 1 |
Tyagi, SC; Veeranki, S | 1 |
Ferrer, I; Janué, A; Odena, MA; Olivé, M; Oliveira, E | 1 |
Alvarez, RB; Askanas, V; Engel, WK; Yang, CC | 1 |
Benson, DW; Fischer, JE; Hasselgren, PO; Hiyama, DT; James, JH; Li, S; Rigel, DF | 1 |
Engel, WK | 1 |
7 other study(ies) available for tyrosine and Muscle Disorders
Article | Year |
---|---|
A novel acceptor stem variant in mitochondrial tRNA
Topics: DNA, Mitochondrial; Electron Transport Complex IV; Humans; Mitochondria; Muscle, Skeletal; Muscular Diseases; Mutation; Oxidative Phosphorylation; Phenotype; RNA, Transfer; Tyrosine | 2020 |
Cysteine mutations cause defective tyrosine phosphorylation in MEGF10 myopathy.
Topics: Amino Acid Motifs; Animals; Binding Sites; Cell Line; Cell Proliferation; CSK Tyrosine-Protein Kinase; Cysteine; Gene Expression Regulation; Membrane Proteins; Mice; Molecular Sequence Data; Muscular Diseases; Mutation; Myoblasts; Phosphorylation; Protein Binding; Protein Interaction Domains and Motifs; Sequence Alignment; Sequence Homology, Amino Acid; Signal Transduction; src-Family Kinases; Tyrosine | 2013 |
Mechanisms of hyperhomocysteinemia induced skeletal muscle myopathy after ischemia in the CBS-/+ mouse model.
Topics: Animals; Antioxidants; Blotting, Western; Cystathionine beta-Synthase; Disease Models, Animal; Homocysteine; Hyperhomocysteinemia; Ischemia; Mice, Inbred C57BL; Models, Biological; Muscle, Skeletal; Muscular Diseases; Nitric Oxide Donors; Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha; PPAR gamma; Protein Binding; Transcription Factors; Tyrosine | 2015 |
Desmin is oxidized and nitrated in affected muscles in myotilinopathies and desminopathies.
Topics: Aged; Aged, 80 and over; Connectin; Cytoskeletal Proteins; Database Management Systems; Desmin; Electrophoresis, Gel, Two-Dimensional; Female; Glycation End Products, Advanced; Humans; Male; Mass Spectrometry; Microfilament Proteins; Middle Aged; Muscle Proteins; Muscular Diseases; Tyrosine | 2007 |
Increase of nitric oxide synthases and nitrotyrosine in inclusion-body myositis.
Topics: Enzyme Induction; Fluorescent Antibody Technique, Indirect; Humans; Immunohistochemistry; Microscopy, Immunoelectron; Muscle Fibers, Skeletal; Muscular Diseases; Myositis, Inclusion Body; Neurons; Nitric Oxide Synthase; Oxidative Stress; Tyrosine | 1996 |
Effect of sepsis on calcium uptake and content in skeletal muscle and regulation in vitro by calcium of total and myofibrillar protein breakdown in control and septic muscle: results from a preliminary study.
Topics: Animals; Calcium; Calcium Radioisotopes; Male; Methylhistidines; Muscle Proteins; Muscles; Muscular Diseases; Myofibrils; Rats; Rats, Inbred Strains; Reference Values; Sepsis; Tyrosine; Verapamil | 1989 |
Selective and nonselective susceptibility of muscle fiber types. A new approach to human neuromuscular diseases.
Topics: Adolescent; Amyotrophic Lateral Sclerosis; Animals; Biopsy; Cats; Dermatomyositis; Esterases; Female; Glucosyltransferases; Glycogen; Guinea Pigs; Histocytochemistry; Humans; Male; Muscular Atrophy; Muscular Diseases; Muscular Dystrophies; Myofibrils; Nervous System Diseases; Oxidoreductases; Paralysis; Rabbits; Schwann Cells; Staining and Labeling; Transferases; Tyrosine | 1970 |