cysteine has been researched along with Long QT Syndrome in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (66.67) | 29.6817 |
| 2010's | 1 (16.67) | 24.3611 |
| 2020's | 1 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Bates, A; Cook, LE; Dabney-Smith, C; Lorigan, GA; Stowe, RB; Travis, EM | 1 |
| Cui, J; Delaloye, K; Nekouzadeh, A; Rudy, Y; Wu, D; Zaydman, MA | 1 |
| Chong, B; Fawkner, M; Hegde, M; Skinner, JR; Webster, DR | 1 |
| Csanády, M; Sepp, R | 1 |
| George, AL; Tapper, AR | 1 |
| Kaback, HR; Sahin-Tóth, M; Weinglass, AB | 1 |
2 review(s) available for cysteine and Long QT Syndrome
| Article | Year |
|---|---|
[The long QT syndrome from the bedside to molecular genetic laboratory. The history of the first described Hungarian family].
Topics: Cysteine; Electrocardiography; ERG1 Potassium Channel; Ether-A-Go-Go Potassium Channels; Genetic Linkage; Genetic Predisposition to Disease; Humans; Hungary; Lod Score; Long QT Syndrome; Mutation, Missense; Pedigree; Tryptophan | 2005 |
The kamikaze approach to membrane transport.
Topics: Alkylation; Amino Acid Sequence; Bacterial Proteins; Binding Sites; Biological Transport; Carrier Proteins; Cysteine; Escherichia coli; Escherichia coli Proteins; Ethylmaleimide; Humans; Lactose; Long QT Syndrome; Membrane Proteins; Membrane Transport Proteins; Metabolism, Inborn Errors; Models, Molecular; Molecular Sequence Data; Monosaccharide Transport Proteins; Mutagenesis, Site-Directed; Protein Conformation; Protons; Recombinant Fusion Proteins; Structure-Activity Relationship; Sulfhydryl Reagents; Symporters | 2001 |
4 other study(ies) available for cysteine and Long QT Syndrome
| Article | Year |
|---|---|
The role of native cysteine residues in the oligomerization of KCNQ1 channels.
Topics: Cysteine; Humans; KCNQ1 Potassium Channel; Long QT Syndrome; Mutation; Potassium Channels, Voltage-Gated | 2023 |
State-dependent electrostatic interactions of S4 arginines with E1 in S2 during Kv7.1 activation.
Topics: Amino Acid Sequence; Animals; Arginine; Cell Membrane; Cysteine; Ion Channel Gating; KCNQ1 Potassium Channel; Long QT Syndrome; Membrane Potentials; Mesylates; Models, Molecular; Molecular Sequence Data; Mutation; Protein Conformation; Protein Structure, Tertiary; Protein Transport; Sulfhydryl Reagents; Surface Properties; Time Factors; Xenopus | 2010 |
Use of the newborn screening card to define cause of death in a 12-year-old diagnosed with epilepsy.
Topics: Arginine; Autopsy; Child; Cysteine; Death, Sudden, Cardiac; DNA Mutational Analysis; Electrocardiography; Genetic Predisposition to Disease; Humans; Infant, Newborn; KCNQ Potassium Channels; KCNQ1 Potassium Channel; Long QT Syndrome; Male; Molecular Diagnostic Techniques; Mutation, Missense; Neonatal Screening; Pedigree; Potassium Channels, Voltage-Gated | 2004 |
Location and orientation of minK within the I(Ks) potassium channel complex.
Topics: Animals; Binding Sites; Cadmium; Cysteine; Humans; KCNQ Potassium Channels; KCNQ1 Potassium Channel; Long QT Syndrome; Mutagenesis; Potassium Channels; Potassium Channels, Voltage-Gated; Protein Binding; Xenopus | 2001 |