ethylnitrosourea has been researched along with Autosomal Dominant Striatonigral Degeneration 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 | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Buchner, DA; Cheng, X; Dib-Hajj, SD; Drews, V; Jones, JM; Justice, MJ; Meisler, MH; Sharkey, LM; Waxman, SG | 1 |
1 other study(ies) available for ethylnitrosourea and Autosomal Dominant Striatonigral Degeneration
Article | Year |
---|---|
The ataxia3 mutation in the N-terminal cytoplasmic domain of sodium channel Na(v)1.6 disrupts intracellular trafficking.
Topics: Animals; Blotting, Western; Cell Line; Chromosome Mapping; Cytoplasm; Data Interpretation, Statistical; DNA, Complementary; Electrophysiology; Ethylnitrosourea; Immunohistochemistry; Machado-Joseph Disease; Mice; Mice, Inbred C57BL; Mutagens; Mutation; Mutation, Missense; NAV1.6 Voltage-Gated Sodium Channel; Nerve Tissue Proteins; Patch-Clamp Techniques; Sciatic Nerve; Sodium Channels; Subcellular Fractions; Transfection | 2009 |