nocodazole has been researched along with Long QT Syndrome in 1 studies
Long QT Syndrome: A condition that is characterized by episodes of fainting (SYNCOPE) and varying degree of ventricular arrhythmia as indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are ROMANO-WARD SYNDROME and JERVELL-LANGE NIELSEN SYNDROME.
| 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 |
|---|---|
| Smith, JL | 1 |
| McBride, CM | 1 |
| Nataraj, PS | 1 |
| Bartos, DC | 1 |
| January, CT | 1 |
| Delisle, BP | 1 |
1 other study available for nocodazole and Long QT Syndrome
| Article | Year |
|---|---|
Trafficking-deficient hERG K⁺ channels linked to long QT syndrome are regulated by a microtubule-dependent quality control compartment in the ER.
Topics: Anti-Arrhythmia Agents; Blotting, Western; Endoplasmic Reticulum; Ether-A-Go-Go Potassium Channels; | 2011 |