thiazolidines has been researched along with Muscular Dystrophy, Duchenne in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 3 (75.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Arthur, PG; Boyatzis, A; Grounds, MD; Terrill, JR | 1 |
| Arthur, PG; Graves, JA; Grounds, MD; Pinniger, GJ; Terrill, JR | 1 |
| Bertoni, C; Jung, ME; Kayali, R; Khitrov, G; Ku, JM; Prikhodko, O | 1 |
| Draviam, RA; Li, J; Wang, B; Watkins, SC; Xiao, X | 1 |
4 other study(ies) available for thiazolidines and Muscular Dystrophy, Duchenne
| Article | Year |
|---|---|
Treatment with the cysteine precursor l-2-oxothiazolidine-4-carboxylate (OTC) implicates taurine deficiency in severity of dystropathology in mdx mice.
Topics: Acetylcysteine; Animals; Disease Models, Animal; Male; Mice; Mice, Inbred C57BL; Muscular Dystrophy, Duchenne; Oxidative Stress; Pyrrolidonecarboxylic Acid; Taurine; Thiazolidines | 2013 |
Increasing taurine intake and taurine synthesis improves skeletal muscle function in the mdx mouse model for Duchenne muscular dystrophy.
Topics: Animals; Disease Models, Animal; Female; Male; Mice; Mice, Inbred C57BL; Mice, Inbred mdx; Muscle Contraction; Muscle, Skeletal; Muscular Dystrophy, Duchenne; Pyrrolidonecarboxylic Acid; Taurine; Thiazolidines | 2016 |
Read-through compound 13 restores dystrophin expression and improves muscle function in the mdx mouse model for Duchenne muscular dystrophy.
Topics: Animals; Codon, Nonsense; Disease Models, Animal; Dose-Response Relationship, Drug; Drug Evaluation, Preclinical; Dystrophin; Furans; Gentamicins; Injections, Intramuscular; Injections, Intraperitoneal; Male; Mice; Mice, Inbred C57BL; Mice, Inbred mdx; Muscle Fibers, Skeletal; Muscle Strength; Muscle, Skeletal; Muscular Dystrophy, Duchenne; Oxadiazoles; Phenols; Protein Synthesis Inhibitors; Reading Frames; Schiff Bases; Thiazolidines; Transcription, Genetic | 2012 |
Mini-dystrophin efficiently incorporates into the dystrophin protein complex in living cells.
Topics: Actins; Active Transport, Cell Nucleus; Bridged Bicyclo Compounds, Heterocyclic; Cell Line; Cell Membrane; Dystroglycans; Dystrophin; Green Fluorescent Proteins; Humans; Macromolecular Substances; Molecular Weight; Muscle Fibers, Skeletal; Muscle, Skeletal; Muscular Dystrophy, Duchenne; Protein Binding; Protein Structure, Tertiary; Protein Transport; Recombinant Fusion Proteins; Sarcolemma; Thiazolidines | 2006 |