| scholarly article | Q13442814 |
| P2093 | author name string | M Jiang | |
| G N Tseng | |||
| J Tseng-Crank | |||
| P2860 | cites work | Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias | Q24311437 |
| KvLQT1, a voltage-gated potassium channel responsible for human cardiac arrhythmias | Q24313536 | ||
| Cloning of a novel component of A-type K+ channels operating at subthreshold potentials with unique expression in heart and brain | Q24314521 | ||
| A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel | Q24316252 | ||
| HERG, a Human Inward Rectifier in the Voltage-Gated Potassium Channel Family | Q24317712 | ||
| Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel | Q24318271 | ||
| A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome | Q24318498 | ||
| Determination of the subunit stoichiometry of a voltage-activated potassium channel | Q28270398 | ||
| Cloning of a membrane protein that induces a slow voltage-gated potassium current | Q28292630 | ||
| K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current | Q28295470 | ||
| Characteristics of the delayed rectifier current (IKr and IKs) in canine ventricular epicardial, midmyocardial, and endocardial myocytes. A weaker IKs contributes to the longer action potential of the M cell | Q34318866 | ||
| Functional role of the NH2-terminal cytoplasmic domain of a mammalian A-type K channel | Q36435270 | ||
| Cloning and expression of the delayed-rectifier IsK channel from neonatal rat heart and diethylstilbestrol-primed rat uterus | Q37738600 | ||
| Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome | Q38348563 | ||
| Specification of subunit assembly by the hydrophilic amino-terminal domain of the Shaker potassium channel | Q46144648 | ||
| Role of the Kv4.3 K+ channel in ventricular muscle. A molecular correlate for the transient outward current | Q48059792 | ||
| Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements. | Q52196602 | ||
| KVLQT1 mutations in three families with familial or sporadic long QT syndrome | Q71689258 | ||
| Drug-induced afterdepolarizations and triggered activity occur in a discrete subpopulation of ventricular muscle cells (M cells) in the canine heart: quinidine and digitalis | Q72721771 | ||
| P433 | issue | 39 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 24109-12 | |
| P577 | publication date | 1997-09-26 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Suppression of slow delayed rectifier current by a truncated isoform of KvLQT1 cloned from normal human heart | |
| P478 | volume | 272 |
| Q44018910 | A truncated splice variant of KCNQ1 cloned from rat heart |
| Q40783466 | Altered state dependence of c-type inactivation in the long and short forms of human Kv1.5. |
| Q34150341 | Alternative splicing of the GABA(A) receptor alpha 4 subunit creates a severely truncated mRNA. |
| Q24297846 | Amino-terminal determinants of U-type inactivation of voltage-gated K+ channels |
| Q40114576 | Contribution of KCNQ1 to the regulatory volume decrease in the human mammary epithelial cell line MCF-7. |
| Q37580457 | Delayed rectifier K(+) currents and cardiac repolarization. |
| Q47853552 | Differential expression of KvLQT1 isoforms across the human ventricular wall |
| Q44922674 | Electrical remodeling in a canine model of ischemic cardiomyopathy |
| Q28204433 | Expression and coassociation of ERG1, KCNQ1, and KCNE1 potassium channel proteins in horse heart |
| Q40293400 | Expression of potassium channel isoforms mRNA in normal human adrenals and aldosterone-secreting adenomas |
| Q48914938 | Functional effects of mutations in KvLQT1 that cause long QT syndrome |
| Q76385043 | IKs, a slow and intriguing cardiac K+ channel and its associated long QT diseases |
| Q33145216 | Inherited long QT syndromes: a paradigm for understanding arrhythmogenesis |
| Q28580389 | Inhibitory effects of volatile anesthetics on currents produced on heterologous expression of KvLQT1 and minK in Xenopus oocytes |
| Q35543305 | KCNQ5/K(v)7.5 potassium channel expression and subcellular localization in primate retinal pigment epithelium and neural retina |
| Q37166829 | Modulation of KCNQ1 alternative splicing regulates cardiac IKs and action potential repolarization. |
| Q33931559 | Molecular basis of functional voltage-gated K+ channel diversity in the mammalian myocardium |
| Q40683514 | Molecular characterization of a two-domain form of the neuronal voltage-gated P/Q-type calcium channel alpha(1)2.1 subunit |
| Q34389321 | Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias |
| Q34206174 | Novel truncated isoform of SK3 potassium channel is a potent dominant-negative regulator of SK currents: implications in schizophrenia. |
| Q34357770 | Pore mutants of HERG and KvLQT1 downregulate the reciprocal currents in stable cell lines |
| Q24316312 | Primary structure and expression of a naturally truncated human P2X ATP receptor subunit from brain and immune system |
| Q73623797 | Properties of the delayed rectifier potassium current in porcine sino-atrial node cells |
| Q34279096 | SK3-1C, a dominant-negative suppressor of SKCa and IKCa channels |
| Q48000452 | Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5. |
| Q28289632 | The KCNQ2 potassium channel: splice variants, functional and developmental expression. Brain localization and comparison with KCNQ3 |
| Q54562154 | Whole blood RNA offers a rapid, comprehensive approach to genetic diagnosis of cardiovascular diseases. |
Search more.