nocodazole has been researched along with Muscular Dystrophies, Limb-Girdle in 2 studies
Muscular Dystrophies, Limb-Girdle: A heterogenous group of inherited muscular dystrophy that can be autosomal dominant or autosomal recessive. There are many forms (called LGMDs) involving genes encoding muscle membrane proteins such as the sarcoglycan (SARCOGLYCANS) complex that interacts with DYSTROPHIN. The disease is characterized by progressing wasting and weakness of the proximal muscles of arms and legs around the HIPS and SHOULDERS (the pelvic and shoulder girdles).
| 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 | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Takada, H | 1 |
| Kaieda, A | 1 |
| Tawada, M | 1 |
| Nagino, T | 1 |
| Sasa, K | 1 |
| Oikawa, T | 1 |
| Oki, A | 1 |
| Sameshima, T | 1 |
| Miyamoto, K | 1 |
| Miyamoto, M | 1 |
| Kokubu, Y | 1 |
| Tozawa, R | 1 |
| Sakurai, H | 1 |
| Saito, B | 1 |
| McDade, JR | 1 |
| Michele, DE | 1 |
2 other studies available for nocodazole and Muscular Dystrophies, Limb-Girdle
| Article | Year |
|---|---|
Identification of 2,6-Disubstituted 3
Topics: Binding Sites; Cell Differentiation; Cell Proliferation; Drug Design; Dysferlin; Hep G2 Cells; Human | 2019 |
Membrane damage-induced vesicle-vesicle fusion of dysferlin-containing vesicles in muscle cells requires microtubules and kinesin.
Topics: Animals; Cell Line; Cell Membrane; Cytoplasmic Vesicles; Green Fluorescent Proteins; Heterocyclic Co | 2014 |