glycerol has been researched along with Long QT Syndrome in 2 studies
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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 | 1 (50.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Zhou, Z | 1 |
| Gong, Q | 1 |
| January, CT | 1 |
| Ficker, E | 1 |
| Thomas, D | 1 |
| Viswanathan, PC | 1 |
| Dennis, AT | 1 |
| Priori, SG | 1 |
| Napolitano, C | 1 |
| Memmi, M | 1 |
| Wible, BA | 1 |
| Kaufman, ES | 1 |
| Iyengar, S | 1 |
| Schwartz, PJ | 1 |
| Rudy, Y | 1 |
| Brown, AM | 1 |
2 other studies available for glycerol and Long QT Syndrome
| Article | Year |
|---|---|
Correction of defective protein trafficking of a mutant HERG potassium channel in human long QT syndrome. Pharmacological and temperature effects.
Topics: Anti-Arrhythmia Agents; Astemizole; Biological Transport; Cation Transport Proteins; Cell Compartmen | 1999 |
Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome.
Topics: Action Potentials; Animals; Cation Transport Proteins; Computer Simulation; DNA-Binding Proteins; El | 2000 |