cycloheximide has been researched along with Ataxias, Hereditary 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 | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Boddeke, E; Duarri, A; Fokkens, MR; Kampinga, HH; Lin, MC; Meijer, M; Nibbeling, EA; Papazian, DM; Sinke, RJ; Smeets, CJ; Verbeek, DS | 1 |
| Boddeke, E; den Dunnen, WF; Duarri, A; Fokkens, M; Hageman, G; Jezierska, J; Kampinga, HH; Kremer, B; Küsters, B; Meijer, M; Schelhaas, HJ; Sinke, RJ; Swertz, MA; van de Vlies, P; van de Warrenburg, BP; van Dijk, F; Verbeek, DS; Verschuuren-Bemelmans, C; Wijmenga, C | 1 |
2 other study(ies) available for cycloheximide and Ataxias, Hereditary
| Article | Year |
|---|---|
Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4.3 channel function and gating in a dominant manner.
Topics: Analysis of Variance; Cycloheximide; DNA Primers; HeLa Cells; Humans; Image Processing, Computer-Assisted; Immunohistochemistry; Mutagenesis, Site-Directed; Mutation; Purkinje Cells; Shal Potassium Channels; Spinocerebellar Degenerations | 2015 |
Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19.
Topics: Aged; Aged, 80 and over; Brain; Case-Control Studies; Chromatin Immunoprecipitation; Cycloheximide; Disease Progression; DNA Mutational Analysis; Family Health; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; HEK293 Cells; HeLa Cells; Humans; Luminescent Proteins; Male; Membrane Potentials; Mutation, Missense; Patch-Clamp Techniques; Protein Synthesis Inhibitors; Shal Potassium Channels; Silver Staining; Spinocerebellar Degenerations; Time Factors; Transfection | 2012 |