Pages that link to "Q34572613"

The following pages link to Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation (Q34572613):

Displaying 42 items.

• Emerging directions in the genetics of atrial fibrillation (Q26852051) (← links)
• Conformational changes of an ion-channel during gating and emerging electrophysiologic properties: Application of a computational approach to cardiac Kv7.1. (Q30383295) (← links)
• Characterization of KCNQ1 atrial fibrillation mutations reveals distinct dependence on KCNE1 (Q30411829) (← links)
• A Novel KCNQ1 Variant (L203P) Associated with Torsades de Pointes–Related Syncope in a Steinert Syndrome Patient (Q33159890) (← links)
• A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation (Q33162279) (← links)
• A contemporary review on the genetic basis of atrial fibrillation (Q33732880) (← links)
• Mechanistic basis for LQT1 caused by S3 mutations in the KCNQ1 subunit of IKs. (Q33814293) (← links)
• Atrial fibrillation in congestive heart failure (Q33954432) (← links)
• Pitx2 prevents susceptibility to atrial arrhythmias by inhibiting left-sided pacemaker specification (Q34006337) (← links)
• Personalized medicine and atrial fibrillation: will it ever happen? (Q34501117) (← links)
• Monogenic atrial fibrillation as pathophysiological paradigms (Q34575292) (← links)
• Genetics of atrial fibrillation: implications for future research directions and personalized medicine (Q34710843) (← links)
• Arrhythmogenic cardiomyopathy in a patient with a rare loss-of-function KCNQ1 mutation (Q35088184) (← links)
• Genetics of atrial fibrillation and possible implications for ischemic stroke. (Q35142380) (← links)
• Your Father and Grandfather's Atrial Fibrillation: A Review of the Genetics of the Most Common Pathologic Cardiac Dysrhythmia (Q35742142) (← links)
• Regulation of Voltage-Activated K( ) Channel Gating by Transmembrane β Subunits (Q35893721) (← links)
• Characterization of a Chinese KCNQ1 mutation (R259H) that shortens repolarization and causes short QT syndrome 2. (Q36011306) (← links)
• The Role of Pharmacogenetics in Atrial Fibrillation Therapeutics: Is Personalized Therapy in Sight? (Q36264955) (← 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)
• New advances in the genetic basis of atrial fibrillation (Q37487799) (← links)
• Atrial fibrillation: the role of common and rare genetic variants (Q37585850) (← links)
• Atrial fibrillation: mechanisms, therapeutics, and future directions (Q37590158) (← links)
• Estrogen receptor 1 gene (TA)n polymorphism is associated with lone atrial fibrillation in men. (Q37620972) (← links)
• Genomics of Atrial Fibrillation (Q37745006) (← links)
• The pharmaceutical pipeline for atrial fibrillation (Q37821928) (← links)
• Genetics of ischemic stroke, stroke-related risk factors, stroke precursors and treatments (Q37998525) (← links)
• Genetics of atrial fibrillation: from families to genomes. (Q38494600) (← links)
• Genetic Discoveries in Atrial Fibrillation and Implications for Clinical Practice (Q38719268) (← links)
• Cardiac Delayed Rectifier Potassium Channels in Health and Disease (Q38854252) (← links)
• Genotype influence in responses to therapy for atrial fibrillation (Q38894994) (← links)
• Relationship between fragmented QRS complexes and left ventricular systolic and diastolic functions. (Q43931907) (← links)
• A KCNQ1 mutation causes age-dependant bradycardia and persistent atrial fibrillation (Q47671957) (← 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)
• Familial clustering of atrial fibrillation and comparative longitudinal outcomes of familial and non-familial atrial fibrillation (Q57260272) (← links)
• Genetics of Atrial Fibrillation (Q58121836) (← links)
• Human Atrial Arrhythmogenesis and Sinus Bradycardia in -Linked Short QT Syndrome: Insights From Computational Modelling (Q58584115) (← links)
• Mechanisms and Drug Development in Atrial Fibrillation (Q60183578) (← links)
• Investigating the Complex Arrhythmic Phenotype Caused by the Gain-of-Function Mutation KCNQ1-G229D (Q64079832) (← links)
• The Genetic Puzzle of Familial Atrial Fibrillation (Q89967824) (← links)