Pages that link to "Q24318897"
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The following pages link to Augmented potassium current is a shared phenotype for two genetic defects associated with familial atrial fibrillation (Q24318897):
Displaying 41 items.
- Natriuretic peptide A (Q302495) (← links)
- Potassium voltage-gated channel subfamily E regulatory subunit 1 (Q1500343) (← links)
- Potassium voltage-gated channel subfamily Q member 1 (Q6449560) (← links)
- Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation (Q21261490) (← links)
- IKs Gain- and Loss-of-Function in Early-Onset Lone Atrial Fibrillation (Q28114836) (← links)
- EHRA/HRS/APHRS/SOLAECE expert consensus on Atrial cardiomyopathies: Definition, characterisation, and clinical implication. (Q30375302) (← links)
- A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation (Q33162279) (← links)
- Brugada syndrome risk loci seem protective against atrial fibrillation (Q34508291) (← links)
- The role of transcription factors in atrial fibrillation (Q35062042) (← links)
- Examining rare and low-frequency genetic variants previously associated with lone or familial forms of atrial fibrillation in an electronic medical record system: a cautionary note. (Q35102106) (← links)
- Large-scale candidate gene analysis in whites and African Americans identifies IL6R polymorphism in relation to atrial fibrillation: the National Heart, Lung, and Blood Institute's Candidate Gene Association Resource (CARe) project (Q35575039) (← links)
- Repolarization recipes for atrial fibrillation: beyond single channel variants (Q35833358) (← links)
- Symptomatic response to antiarrhythmic drug therapy is modulated by a common single nucleotide polymorphism in atrial fibrillation. (Q36139922) (← links)
- Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation (Q36252497) (← links)
- The Role of Pharmacogenetics in Atrial Fibrillation Therapeutics: Is Personalized Therapy in Sight? (Q36264955) (← links)
- A KCNJ8 mutation associated with early repolarization and atrial fibrillation (Q36280780) (← links)
- Probing the structural basis for differential KCNQ1 modulation by KCNE1 and KCNE2 (Q36446422) (← links)
- TBX5 mutations contribute to early-onset atrial fibrillation in Chinese and Caucasians (Q36575699) (← links)
- Functional modeling in zebrafish demonstrates that the atrial-fibrillation-associated gene GREM2 regulates cardiac laterality, cardiomyocyte differentiation and atrial rhythm (Q36683034) (← links)
- Screening of the ito regulatory subunit klf15 in patients with early-onset lone atrial fibrillation (Q36850495) (← links)
- Genetic mechanisms of atrial fibrillation: impact on response to treatment (Q36876093) (← links)
- R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation (Q36996166) (← links)
- [Ca2+]i elevation and oxidative stress induce KCNQ1 protein translocation from the cytosol to the cell surface and increase slow delayed rectifier (IKs) in cardiac myocytes (Q37368682) (← links)
- Selective targeting of gain-of-function KCNQ1 mutations predisposing to atrial fibrillation (Q37481774) (← links)
- Atrial fibrillation: the role of common and rare genetic variants (Q37585850) (← links)
- Candidate gene approach to identifying rare genetic variants associated with lone atrial fibrillation (Q37626338) (← links)
- Personalized medicine to treat arrhythmias (Q38203726) (← links)
- Genetics of atrial fibrillation: from families to genomes. (Q38494600) (← links)
- Transient Notch Activation Induces Long-Term Gene Expression Changes Leading to Sick Sinus Syndrome in Mice (Q38695345) (← links)
- An allosteric mechanism for drug block of the human cardiac potassium channel KCNQ1. (Q39236123) (← links)
- Lone AF - Etiologic Factors and Genetic Insights into Pathophysiolgy (Q39300535) (← links)
- Investigating genomic and phenotypic parallelism between piscivorous and planktivorous lake trout (Salvelinus namaycush) ecotypes by means of RADseq and morphometrics analyses (Q44866004) (← links)
- EHRA/HRS/APHRS/SOLAECE expert consensus on atrial cardiomyopathies: definition, characterization, and clinical implication. (Q45939560) (← links)
- Pro-arrhythmogenic effects of the S140G KCNQ1 mutation in human atrial fibrillation - insights from modelling. (Q47895566) (← links)
- Polymorphisms but not mutations of the KCNQ1 gene are associated with lone atrial fibrillation in the Chinese Han population. (Q55114202) (← links)
- EHRA/HRS/APHRS/SOLAECE expert consensus on atrial cardiomyopathies: Definition, characterization, and clinical implication. (Q55638585) (← links)
- Genetics of Atrial Fibrillation (Q58121836) (← links)
- Mechanisms and Drug Development in Atrial Fibrillation (Q60183578) (← links)
- Next-generation sequencing of 100 candidate genes in young victims of suspected sudden cardiac death with structural abnormalities of the heart (Q63729245) (← links)
- Atrial fibrillation symptom profiles associated with healthcare utilization: A latent class regression analysis (Q88386985) (← links)
- Whole-exome sequencing of Finnish patients with vascular cognitive impairment (Q103836788) (← links)