Page last updated: 2024-08-21

ethylnitrosourea and Autosomal Dominant Striatonigral Degeneration

ethylnitrosourea has been researched along with Autosomal Dominant Striatonigral Degeneration in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Buchner, DA; Cheng, X; Dib-Hajj, SD; Drews, V; Jones, JM; Justice, MJ; Meisler, MH; Sharkey, LM; Waxman, SG1

Other Studies

1 other study(ies) available for ethylnitrosourea and Autosomal Dominant Striatonigral Degeneration

ArticleYear
The ataxia3 mutation in the N-terminal cytoplasmic domain of sodium channel Na(v)1.6 disrupts intracellular trafficking.
    The Journal of neuroscience : the official journal of the Society for Neuroscience, 2009, Mar-04, Volume: 29, Issue:9

    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