A novel mutation in the HCN4 gene causes symptomatic sinus bradycardia in Moroccan Jews.
about
Hyperpolarization-activated current, If, in mathematical models of rabbit sinoatrial node pacemaker cellsFunny channel gene mutations associated with arrhythmiasPacemaker activity of the human sinoatrial node: an update on the effects of mutations in HCN4 on the hyperpolarization-activated currentA molecular signature of tissues with pacemaker activity in the heart and upper urinary tract involves coexpressed hyperpolarization-activated cation and T-type Ca2+ channels.Pacemaker current inhibition in experimental human cardiac sympathetic activation: a double-blind, randomized, crossover study.Genetics and Sinus Node Dysfunction.Resting heart rate and risk of sudden cardiac death in the general population: influence of left ventricular systolic dysfunction and heart rate-modulating drugs.Overview of Basic Mechanisms of Cardiac ArrhythmiaA natural polymorphism alters odour and DEET sensitivity in an insect odorant receptorThe genetic basis for inherited forms of sinoatrial dysfunction and atrioventricular node dysfunctionTranscription factor ISL1 is essential for pacemaker development and function.Biology of the Sinus Node and its Disease.The Brady Bunch? New evidence for nominative determinism in patients' health: retrospective, population based cohort study.Exploring HCN channels as novel drug targets.Computational analysis of the human sinus node action potential: model development and effects of mutations.HCN4, Sinus Bradycardia and Atrial Fibrillation.Hyperpolarization-activated cation and T-type calcium ion channel expression in porcine and human renal pacemaker tissues.Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm.If Channel as an Emerging Therapeutic Target for Cardiovascular Diseases: A Review of Current Evidence and Controversies.The HCN4 channel mutation D553N associated with bradycardia has a C-linker mediated gating defect.Mutation in S6 domain of HCN4 channel in patient with suspected Brugada syndrome modifies channel function.
P2860
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P2860
A novel mutation in the HCN4 gene causes symptomatic sinus bradycardia in Moroccan Jews.
description
2010 nî lūn-bûn
@nan
2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
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2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
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name
A novel mutation in the HCN4 gene causes symptomatic sinus bradycardia in Moroccan Jews.
@ast
A novel mutation in the HCN4 gene causes symptomatic sinus bradycardia in Moroccan Jews.
@en
A novel mutation in the HCN4 gene causes symptomatic sinus bradycardia in Moroccan Jews.
@nl
type
label
A novel mutation in the HCN4 gene causes symptomatic sinus bradycardia in Moroccan Jews.
@ast
A novel mutation in the HCN4 gene causes symptomatic sinus bradycardia in Moroccan Jews.
@en
A novel mutation in the HCN4 gene causes symptomatic sinus bradycardia in Moroccan Jews.
@nl
prefLabel
A novel mutation in the HCN4 gene causes symptomatic sinus bradycardia in Moroccan Jews.
@ast
A novel mutation in the HCN4 gene causes symptomatic sinus bradycardia in Moroccan Jews.
@en
A novel mutation in the HCN4 gene causes symptomatic sinus bradycardia in Moroccan Jews.
@nl
P2093
P2860
P50
P1476
A novel mutation in the HCN4 gene causes symptomatic sinus bradycardia in Moroccan Jews
@en
P2093
Avishag Laish-Farkash
David Luria
Dina Marek-Yagel
Dovrat Brass
Haya Reznik
Michael Eldar
Michael Glikson
P2860
P304
P356
10.1111/J.1540-8167.2010.01844.X
P577
2010-12-01T00:00:00Z