nocodazole has been researched along with Amyotrophic Lateral Sclerosis in 2 studies
Amyotrophic Lateral Sclerosis: A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94)
| 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 | 1 (50.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Watanabe, S | 1 |
| Inami, H | 1 |
| Oiwa, K | 1 |
| Murata, Y | 1 |
| Sakai, S | 1 |
| Komine, O | 1 |
| Sobue, A | 1 |
| Iguchi, Y | 1 |
| Katsuno, M | 1 |
| Yamanaka, K | 1 |
| Vilmont, V | 1 |
| Cadot, B | 1 |
| Vezin, E | 1 |
| Le Grand, F | 1 |
| Gomes, ER | 1 |
2 other studies available for nocodazole and Amyotrophic Lateral Sclerosis
| Article | Year |
|---|---|
Aggresome formation and liquid-liquid phase separation independently induce cytoplasmic aggregation of TAR DNA-binding protein 43.
Topics: Amyotrophic Lateral Sclerosis; Animals; DNA-Binding Proteins; HEK293 Cells; HeLa Cells; Histone Deac | 2020 |
Dynein disruption perturbs post-synaptic components and contributes to impaired MuSK clustering at the NMJ: implication in ALS.
Topics: Agrin; Amyotrophic Lateral Sclerosis; Animals; Cell Differentiation; Cells, Cultured; Disease Models | 2016 |