lysine has been researched along with Long QT Syndrome in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (75.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ba, Y; Huang, X; Karush, JM; Lian, J; Liu, N; Lu, X; Mao, H; Wang, Y; Yang, X; Zhou, J | 1 |
| Carmeliet, E; Carmeliet, P; Collen, D; Devriendt, K; Gewillig, M; Heidbüchel, H; Jongbloed, RJ; Mubagwa, K; Rossenbacker, T; Vereecke, J | 1 |
| Carmeliet, P; Fredj, S; Kass, RS; Lindegger, N; Sampson, KJ | 1 |
| Benndorf, K; Figulla, HR; Hensellek, S; Prochnau, D; Surber, R; Werner, GS; Zimmer, T | 1 |
4 other study(ies) available for lysine and Long QT Syndrome
| Article | Year |
|---|---|
Pharmacologic Approach to Defective Protein Trafficking in the E637K-hERG Mutant with PD-118057 and Thapsigargin.
Topics: Amino Acid Substitution; Chlorobenzenes; Endoplasmic Reticulum Stress; ERG1 Potassium Channel; Glutamic Acid; HEK293 Cells; Humans; Long QT Syndrome; Lysine; Mutant Proteins; Mutation, Missense; ortho-Aminobenzoates; Patch-Clamp Techniques; Protein Transport; Thapsigargin; Unfolded Protein Response | 2013 |
Novel mutation in the Per-Arnt-Sim domain of KCNH2 causes a malignant form of long-QT syndrome.
Topics: Adult; Blotting, Western; Cell Line; Death, Sudden, Cardiac; Electrophysiology; ERG1 Potassium Channel; Ether-A-Go-Go Potassium Channels; Female; Glutamic Acid; Humans; Kidney; Long QT Syndrome; Lysine; Male; Microscopy, Confocal; Middle Aged; Mutation, Missense; Patch-Clamp Techniques; Pedigree; Peptides; Phenotype; Piperidines; Potassium Channels, Voltage-Gated; Protein Structure, Tertiary; Proteins; Pyridines | 2005 |
Altered Na+ channels promote pause-induced spontaneous diastolic activity in long QT syndrome type 3 myocytes.
Topics: Animals; Anti-Arrhythmia Agents; Diastole; Electrophysiology; Flecainide; Gene Deletion; Genetic Variation; Glutamine; Heart; Long QT Syndrome; Lysine; Mice; Mice, Transgenic; Myocytes, Cardiac; Patch-Clamp Techniques; Proline; Sodium Channels | 2006 |
Combination of cardiac conduction disease and long QT syndrome caused by mutation T1620K in the cardiac sodium channel.
Topics: Action Potentials; Adolescent; Adult; Ajmaline; Animals; Anti-Arrhythmia Agents; Bundle-Branch Block; Cell Line; Child; Death, Sudden, Cardiac; DNA Mutational Analysis; Electrocardiography; Female; Gene Transfer Techniques; Genetic Predisposition to Disease; Humans; Kinetics; Lidocaine; Long QT Syndrome; Lysine; Male; Muscle Proteins; Mutation; Myocardium; NAV1.5 Voltage-Gated Sodium Channel; Patch-Clamp Techniques; Pedigree; Sodium; Sodium Channels; Syncope; Threonine; Xenopus laevis | 2008 |