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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
 

Your search matched a total of 64 documents. Results 1 - 10.

Homo sapiens
Gene: ... primers based on exon- flanking sequences amplify all SCN5A exons by PCR. Sequence analysis has indicated...Disease relevance of SCN5A SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses...
Canis lupus familiaris
Gene: ... Disease relevance of SCN5A BACKGROUND: This study examines the contribution of transmural... channel block under conditions mimicking HERG and SCN5A defects linked to the congenital long- QT syndrome( LQTS). High impact information on SCN5A Our aim was to determine if Na (+) currents and message...
Mus musculus
Gene: ... Disease relevance of Scn5a CONCLUSIONS: A 50% reduction in Scn5a expression alone or age- related interstitial fibrosis only slightly affects conduction. INTRODUCTION: Gain- of- function mutations within Scn5a.... High impact information on Scn5a Slowed conduction and ventricular tachycardia after targeted...
MeSH term: ... to SCN5A mutational analyses. Analytical, diagnostic and therapeutic context of Myocardium... and cardiac muscle, anti- MLCK decorated the actin- containing I bands of the sarcomere. Because all the known... milieu, and altered glycoside- binding properties of( Na++ K +)- ATPase all participate in the reduction...
MeSH term: ... Assessment( Health Care) MAIN OUTCOME MEASURES: Molecular and functional characterization of SCN5A defects... -- independently predicted all three outcome measures. The women underwent serial proton magnetic resonance...
MeSH term: ... in African Americans, SCN5A S1103Y. Similar high blood pressure accompanied by a low systemic renin state..., but there was significant heterogeneity in ORs among studies of African Americans( P <. 03). Here we studied SCN5A... additional mutations in the coding region of the CCR5 gene, all but 3 of which are codon altering or...
MeSH term: ... channel gene( SCN5A) defects have an increased frequency of cardiac events during sleep, and a recent case is reported of a sporadic SCN5A mutation in an infant with near SIDS, SCN5A has emerged as the leading... possessed SCN5A mutations: a 6- week- old white male with an A997S missense mutation in exon 17 and a 1...
MeSH term: ... intervals on baseline ECG in patients with established SCN5A mutations( PQ and HV interval and, upon class I...) and to the decrease in the extent of myocardial ischemia observed in all 12 ECG leads( r=- 0. 61) compared... trials. High impact information on Electrocardiography PATIENTS: All symptomatic patients who underwent...
MeSH term: ... the thin- filament contractile protein cardiac troponin T are responsible for 15% of all cases of familial hypertrophic cardiomyopathy, the leading cause of sudden death in young athletes. We have screened SCN5A... routinely applied to all infarct survivors with depressed ventricular function, a therapy that reduces...
MeSH term: ... . Role of SCN5A Y1102 polymorphism in sudden cardiac death in blacks. Analytical, diagnostic... doses of cocaine severely depressed all cardiac parameters and its effect on the isolated heart, cocaine... lower all- cause mortality( 30 vs. 49, HR= 0. 67, 95% CI 0. 42 to 1. 06, p= 0. 090) and fewer pacemaker...

 

 
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