Mapping of a gene for long QT syndrome to chromosome 4q25-27
about
Molecular cloning and functional expression of a novel human gene encoding two 41-43 kDa skeletal muscle internal membrane proteinsA cardiac arrhythmia syndrome caused by loss of ankyrin-B functionIon Channels in the HeartDefective interactions of protein partner with ion channels and transporters as alternative mechanisms of membrane channelopathiesCongenital Long QT Syndrome: An Update and Present Perspective in Saudi Arabia.Nav1.5/R1193Q polymorphism is associated with both long QT and Brugada syndromes.Congenital and drug-induced long-QT syndrome: an update.Novel Variant in the ANK2 Membrane-Binding Domain Is Associated With Ankyrin-B Syndrome and Structural Heart Disease in a First Nations Population With a High Rate of Long QT Syndrome.Oxidized calmodulin kinase II regulates conduction following myocardial infarction: a computational analysis.Evidence of a long QT founder gene with varying phenotypic expression in South African families.Ankyrin-B is required for intracellular sorting of structurally diverse Ca2+ homeostasis proteins.Antiarrhythmics--from cell to clinic: past, present, and future.From Fifth Business to Protagonist: the complex roles of ion channel anchors in cardiac arrhythmia.Defining a new paradigm for human arrhythmia syndromes: phenotypic manifestations of gene mutations in ion channel- and transporter-associated proteins.Defining new insight into atypical arrhythmia: a computational model of ankyrin-B syndromeAtrial fibrillation and sinus node dysfunction in human ankyrin-B syndrome: a computational analysis.Personalized medicine and atrial fibrillation: will it ever happen?Cardiac ankyrins in health and diseaseCalcium and arrhythmogenesis.Coordinating electrical activity of the heart: ankyrin polypeptides in human cardiac disease.LQT4 gene: the "missing" ankyrin.Genetic polymorphisms in KCNQ1, HERG, KCNE1 and KCNE2 genes in the Chinese, Malay and Indian populations of SingaporeThe phenotype/genotype relation and the current status of genetic screening in hypertrophic cardiomyopathy, Marfan syndrome, and the long QT syndrome.In silico investigations on functional and haplotype tag SNPs associated with congenital long QT syndromes (LQTSs)Analysis of genetic and non-genetic factors that affect the QTc interval in a Mongolian population: the GENDISCAN studyGenotype- and phenotype-guided management of congenital long QT syndrome.An introduction to murine models of atrial fibrillationMolecular Pathophysiology of Congenital Long QT Syndrome.Murine Electrophysiological Models of Cardiac Arrhythmogenesis.Long QT syndrome: from channels to cardiac arrhythmias.Is long QT syndrome entering the era of molecular diagnosis?Ankyrins and Spectrins in Cardiovascular Biology and Disease.The evolving role of ankyrin-B in cardiovascular disease.Long QT Syndrome and Sinus Bradycardia-A Mini Review
P2860
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P2860
Mapping of a gene for long QT syndrome to chromosome 4q25-27
description
1995 nî lūn-bûn
@nan
1995 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Mapping of a gene for long QT syndrome to chromosome 4q25-27
@ast
Mapping of a gene for long QT syndrome to chromosome 4q25-27
@en
Mapping of a gene for long QT syndrome to chromosome 4q25-27
@nl
type
label
Mapping of a gene for long QT syndrome to chromosome 4q25-27
@ast
Mapping of a gene for long QT syndrome to chromosome 4q25-27
@en
Mapping of a gene for long QT syndrome to chromosome 4q25-27
@nl
prefLabel
Mapping of a gene for long QT syndrome to chromosome 4q25-27
@ast
Mapping of a gene for long QT syndrome to chromosome 4q25-27
@en
Mapping of a gene for long QT syndrome to chromosome 4q25-27
@nl
P2093
P2860
P1476
Mapping of a gene for long QT syndrome to chromosome 4q25-27
@en
P2093
Bouhour JB
Charpentier F
Donnelly P
P2860
P304
P407
P577
1995-11-01T00:00:00Z