Keywords: Genome-wide association; Myocardial infarction; Coronary artery disease; Haplotypes; Heritability; CDKN2A/B; CXCL12; KCNE2;
مقالات ISI (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
How do sex hormones modify arrhythmogenesis in long QT syndrome? Sex hormone effects on arrhythmogenic substrate and triggered activity
Keywords: APD; action potential duration; EAD; early afterdepolarization; ICa,L; L-type Ca2+ current; IK1; inward rectifier K+ current; IKr; rapid delayed rectifier K+ current; IKs; slow delayed rectifier K+ current; KCNE1; β-subunit to KvLQT1 to form slow delayed
KCNE2 modulates cardiac L-type Ca2Â + channel
Keywords: LCC; L-type Ca2 + channel; LQT; long-QT syndrome; ICa,L; L-type Ca2 + current; AF; atrial fibrillation; NTI; N-terminal inhibitory module; KCNE2; L-type  Ca2+ current; Cav1.2; KCNE2 mutation; Familial atrial fibrillation;
Cardiac arrhythmia and thyroid dysfunction: A novel genetic link
Keywords: Atrial fibrillation; Hypothyroidism; Hyperthyroidism; KCNE2; KCNQ1; Long QT Syndrome; MiRP1
Structural basis for KV7.1–KCNEx interactions in the IKs channel complex
Keywords: IKs; KCNE1; KCNE2; KCNQ1; KV7.1IKr, cardiac rapid delayed rectifier current; IKs, cardiac slow delayed rectifier current; KV, voltage-gated potassium channel; NMR, nuclear magnetic resonance; PIP2, phosphatidylinositol 4,5-bisphosphate
KCNE2 modulation of Kv4.3 current and its potential role in fatal rhythm disorders
Keywords: Cardiac arrhythmia; M54T variation; I57T variation; KCNE2; Kv4.3; Sudden cardiac deathCHO, Chinese hamster ovary; HERG, human ether-a-go-go related gene; WT, wild type
An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome
Keywords: Long QT syndrome; KCNQ1; Intronic mutation; Hearing rescue; SCN5A; sodium channel, voltage-gated, type V, alpha subunit; KCNH2; potassium voltage-gated channel, subfamily H (eag-related), member 2; KCNQ1; potassium voltage-gated channel, KQT-like subfamil
Hormonal regulation of cardiac KCNE2 gene expression
Keywords: KCNE2; MiRP1; Promoter; Estrogen; ERE; Estrogen receptor alpha
Molecular aspects of the congenital and acquired Long QT Syndrome: Clinical implications
Keywords: Ion channel; Long QT Syndrome; Arrhythmia; Sudden cardiac death; hERG; KCNQ1; SCN5A; KCNE1; KCNE2; CACNA1c; KCNJ2; Genotype; Phenotype; Congenital; Acquired; Torsade de pointes
KCNQ1 mutation Q147R is associated with atrial fibrillation and prolonged QT interval
Keywords: Arrhythmia; Atrial fibrillation; QT interval; Potassium channel; Kv7.1; KCNQ1; KCNE1; KCNE2; Two-electrode voltage clamp
Modulation of functional properties of KCNQ1 channel by association of KCNE1 and KCNE2
Keywords: IKs; KCNE1; KCNE2; KCNQ1; Mefenamic acid; Long QT syndrome; K+ channel; Heart; Patch–clamp
Expression and transcriptional control of human KCNE genes
Keywords: Potassium channel; Promoter; KCNE1; KCNE2; KCNE3; KCNE4; KCNE5; KCNQ1
Expression of multiple KCNE genes in human heart may enable variable modulation of IKs
Keywords: Potassium channel; KCNQ1; KCNE1; KCNE2; KCNE3; KCNE4; KCNE5;