mimosine has been researched along with Muscular Atrophy, Spinal in 1 studies
Mimosine: 3-Hydroxy-4-oxo-1(4H)-pyridinealanine. An antineoplastic alanine-substituted pyridine derivative isolated from Leucena glauca.
Muscular Atrophy, Spinal: A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Lefebvre, S | 1 |
| Burlet, P | 1 |
| Viollet, L | 1 |
| Bertrandy, S | 1 |
| Huber, C | 1 |
| Belser, C | 1 |
| Munnich, A | 1 |
1 other study available for mimosine and Muscular Atrophy, Spinal
| Article | Year |
|---|---|
A novel association of the SMN protein with two major non-ribosomal nucleolar proteins and its implication in spinal muscular atrophy.
Topics: Animals; Antineoplastic Agents; Cell Nucleolus; Cells, Cultured; COS Cells; Cyclic AMP Response Elem | 2002 |