Common candidate gene variants are associated with QT interval duration in the general population.
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Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studiesRING finger protein RNF207, a novel regulator of cardiac excitationNitric Oxide Synthase 1 Adaptor Protein, an Emerging New Genetic Marker for QT Prolongation and Sudden Cardiac DeathTox-database.net: a curated resource for data describing chemical triggered in vitro cardiac ion channels inhibition.KCNQ1 p.L353L affects splicing and modifies the phenotype in a founder population with long QT syndrome type 1.Sex is a moderator of the association between NOS1AP sequence variants and QTc in two long QT syndrome founder populations: a pedigree-based measured genotype association analysis.Relationship of common candidate gene variants to electrocardiographic T-wave peak to T-wave end interval and T-wave morphology parameters.KCNE1 D85N polymorphism--a sex-specific modifier in type 1 long QT syndrome?Review of the Diabetes Heart Study (DHS) family of studies: a comprehensively examined sample for genetic and epidemiological studies of type 2 diabetes and its complications.Genetic analysis, in silico prediction, and family segregation in long QT syndrome.Epidemiologic, molecular, and functional evidence suggest A572D-SCN5A should not be considered an independent LQT3-susceptibility mutation.Long QT interval in Turner syndrome--a high prevalence of LQTS gene mutationsCommon genetic variants, QT interval, and sudden cardiac death in a Finnish population-based study.Common variants in CASQ2, GPD1L, and NOS1AP are significantly associated with risk of sudden death in patients with coronary artery disease.A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointesWild type and K897T polymorphisms of the hERG gene: modeling the APD in Caucasians.Dysfunctional potassium channel subunit interaction as a novel mechanism of long QT syndrome.A common variant near the KCNJ2 gene is associated with T-peak to T-end interval.KCNE genetics and pharmacogenomics in cardiac arrhythmias: much ado about nothing?Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population.Common variants at ten loci influence QT interval duration in the QTGEN StudyAn Examination of KCNE1 Mutations and Common Variants in Chronic Tinnitus.KCNH2 pharmacogenomics summary.Long QT syndrome: beyond the causal mutation.Non optical semi-conductor next generation sequencing of the main cardiac QT-interval duration genes in pooled DNA samples.The role of known variants of KCNQ1, KCNH2, KCNE1, SCN5A, and NOS1AP in water-related deaths.Common variants in the hERG (KCNH2) voltage-gated potassium channel are associated with altered fasting and glucose-stimulated plasma incretin and glucagon responses.Mutation analysis for the detection of long QT-syndrome (LQTS) associated SNPs.herg1b expression as a potential specific marker in pediatric acute myeloid leukemia patients with HERG 897K/K genotype.
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P2860
Common candidate gene variants are associated with QT interval duration in the general population.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on April 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Common candidate gene variants ...... ion in the general population.
@en
Common candidate gene variants ...... ion in the general population.
@nl
type
label
Common candidate gene variants ...... ion in the general population.
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Common candidate gene variants ...... ion in the general population.
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Common candidate gene variants ...... ion in the general population.
@en
Common candidate gene variants ...... ion in the general population.
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P2093
P2860
P1476
Common candidate gene variants ...... ion in the general population.
@en
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A Marjamaa
A Reunanen
C Newton-Cheh
H Väänänen
P2860
P304
P356
10.1111/J.1365-2796.2008.02026.X
P407
P577
2009-04-01T00:00:00Z