nad has been researched along with Inclusion Body Myopathy, Sporadic in 1 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 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Abramov, AY; Bartolome, F; Burchell, VS; Calvo, A; Canosa, A; ChiĆ², A; Fox, NC; Hardy, J; Houlden, H; Mahoney, CJ; Mandrioli, J; Moglia, C; Orrell, RW; Plun-Favreau, H; Preza, E; Wray, S; Wu, HC | 1 |
1 other study(ies) available for nad and Inclusion Body Myopathy, Sporadic
Article | Year |
---|---|
Pathogenic VCP mutations induce mitochondrial uncoupling and reduced ATP levels.
Topics: Adenosine Triphosphatases; Adenosine Triphosphate; Adult; Aged; Analysis of Variance; Animals; Animals, Newborn; Case-Control Studies; Cell Cycle Proteins; Cells, Cultured; Cerebral Cortex; Family Health; Female; Fibroblasts; Frontotemporal Dementia; Humans; Lipid Peroxidation; Luminescent Proteins; Magnesium; Male; Membrane Potential, Mitochondrial; Mice; Mice, Inbred C57BL; Middle Aged; Mitochondria; Muscular Dystrophies, Limb-Girdle; Mutation; Myositis, Inclusion Body; NAD; Neuroblastoma; Neurons; Osteitis Deformans; Oxygen Consumption; RNA, Small Interfering; Transfection; Valosin Containing Protein | 2013 |