lysine has been researched along with Adult Spinal Muscular Atrophy in 2 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 | 1 (50.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Binda, O; Corpet, A; Côté, J; Fradet-Turcotte, A; Galloy, M; Jacquet, K; Kimenyi Ishimwe, AB; Lomonte, P | 1 |
| Baloh, RH; Bouitbir, J; Dupuis, L; Eschbach, J; Fergani, A; Geny, B; Harms, MB; Larmet, Y; Loeffler, JP; Ludolph, AC; Marion, V; Messadeq, N; René, F; Schlagowski, AI; Shy, ME; Sinniger, J; Weydt, P; Zoll, J | 1 |
2 other study(ies) available for lysine and Adult Spinal Muscular Atrophy
| Article | Year |
|---|---|
The TUDOR domain of SMN is an H3K79
Topics: Arginine; Histone Code; Humans; Infant; Lysine; Muscular Atrophy, Spinal; RNA Polymerase II; Survival of Motor Neuron 1 Protein; Transcription Factors | 2023 |
Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age.
Topics: Aging; Animals; Cells, Cultured; Cytoplasmic Dyneins; Embryo, Mammalian; Female; Glucagon; Glutamic Acid; Humans; Insulin; Lysine; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Mitochondria; Muscular Atrophy, Spinal; Mutation; Superoxide Dismutase; Superoxide Dismutase-1; Transfection | 2013 |