cysteine has been researched along with Becker Muscular Dystrophy in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 5 (71.43) | 24.3611 |
| 2020's | 2 (28.57) | 2.80 |
| Authors | Studies |
|---|---|
| Day, NJ; Fillmore, TL; Gaffrey, MJ; Moore, RJ; Qian, WJ; Rodney, GG; Zhang, T; Zhao, R | 1 |
| Ellwood, RA; Etheridge, T; Lewis, J; Piasecki, M; Slade, L; Sudevan, S; Szewczyk, NJ; Torregrossa, R; Whiteman, M | 1 |
| Contreras, JE; Fraidenraich, D; Himelman, E; Lillo, MA; Shirokova, N; Xie, LH | 1 |
| Bedja, D; Chung, HS; Holewinski, RJ; Kass, DA; Kim, GE; Van Eyk, JE; Venkatraman, V; Zhu, G | 1 |
| Ervasti, JM; Findlay, AR; Flanigan, KM; Howard, MT; Johnson, EK; Kaminoh, YJ; Maiti, B; Montanaro, F; Ray, WC; Simmons, TR; Strandjord, DM; Taylor, LE; Vulin, A; Wein, N | 1 |
| Arthur, PG; Grounds, MD; Terrill, JR | 1 |
| Armstrong, AE; Arthur, PG; El-Shafey, AF; Grounds, MD; Terrill, JR | 1 |
7 other study(ies) available for cysteine and Becker Muscular Dystrophy
| Article | Year |
|---|---|
A deep redox proteome profiling workflow and its application to skeletal muscle of a Duchenne Muscular Dystrophy model.
Topics: Animals; Cysteine; Mice; Mice, Inbred mdx; Muscle, Skeletal; Muscular Dystrophy, Duchenne; Oxidation-Reduction; Proteome; Sulfhydryl Compounds; Workflow | 2022 |
Sulfur amino acid supplementation displays therapeutic potential in a C. elegans model of Duchenne muscular dystrophy.
Topics: Animals; Caenorhabditis elegans; Cysteine; Dietary Supplements; Muscular Dystrophy, Duchenne; Sulfur | 2022 |
S-nitrosylation of connexin43 hemichannels elicits cardiac stress-induced arrhythmias in Duchenne muscular dystrophy mice.
Topics: Adrenergic beta-Agonists; Animals; Arrhythmias, Cardiac; Cell Membrane; Cell Membrane Permeability; Connexin 43; Cysteine; Disease Models, Animal; Dystrophin; Evoked Potentials; Humans; Isoproterenol; Male; Membrane Potentials; Mice; Mice, Inbred mdx; Mice, Transgenic; Muscular Dystrophy, Duchenne; Mutation; Myocytes, Cardiac; Nitric Oxide; Oocytes; Patch-Clamp Techniques; Xenopus laevis | 2019 |
Transient receptor potential channel 6 regulates abnormal cardiac S-nitrosylation in Duchenne muscular dystrophy.
Topics: Animals; Calcium Signaling; Cysteine; Disease Models, Animal; Epinephrine; Gene Deletion; Male; Mice; Mice, Inbred C57BL; Muscular Dystrophy, Duchenne; Myocardium; Nitrosation; S-Nitrosothiols; Sympathomimetics; TRPC Cation Channels; TRPC6 Cation Channel; Ventricular Remodeling | 2017 |
The ZZ domain of dystrophin in DMD: making sense of missense mutations.
Topics: Actins; Animals; Aspartic Acid; Cysteine; Dystroglycans; Dystrophin; Genetic Variation; Humans; Mice; Mice, Transgenic; Muscular Dystrophy, Duchenne; Mutation, Missense; Protein Folding; Protein Stability; Zinc Fingers | 2014 |
Taurine deficiency, synthesis and transport in the mdx mouse model for Duchenne Muscular Dystrophy.
Topics: Animals; Biological Transport; Chromatography, High Pressure Liquid; Cysteine; Disease Models, Animal; Dystrophin; Humans; Immunoblotting; Kidney; Liver; Male; Mice, Inbred C57BL; Mice, Inbred mdx; Muscle, Skeletal; Muscular Dystrophy, Animal; Muscular Dystrophy, Duchenne; Taurine; Time Factors | 2015 |
Screening for increased protein thiol oxidation in oxidatively stressed muscle tissue.
Topics: Animals; Cysteine; Glutathione; Lipid Peroxidation; Male; Malondialdehyde; Mice; Mice, Inbred C57BL; Mice, Inbred mdx; Muscle, Skeletal; Muscular Dystrophy, Duchenne; Oxidation-Reduction; Oxidative Stress; Protein Carbonylation; Proteins; Sulfhydryl Compounds | 2011 |