'KCNQ' can also refer to...


Potassium Channels (Including KCNQ) and Epilepsy

KCNQ1 autoantibodies: another way to regulate I Ks

New KCNQ1 mutations leading to haploinsufficiency in a general population Defective trafficking of a KvLQT1 mutant

KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum

In vitro molecular interactions and distribution of KCNE family with KCNQ1 in the human heart

Abnormal KCNQ1 trafficking influences disease pathogenesis in hereditary long QT syndromes (LQT1)

De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero

Functional effects of a KCNQ1 mutation associated with the long QT syndrome

IGF2, H19, CDKNIC, KCNQ1OT1, and the Beckwith-Wiedemann Syndrome

LQT1 mutations in KCNQ1 C-terminus assembly domain suppress I Ks using different mechanisms

I Ks response to protein kinase A-dependent KCNQ1 phosphorylation requires direct interaction with microtubules

Functional suppression of Kcnq1 leads to early sodium channel remodelling and cardiac conduction system dysmorphogenesis

Obesity and ischemic stroke modulate the methylation levels of KCNQ1 in white blood cells

Heightened susceptibility to chronic gastritis, hyperplasia and metaplasia in Kcnq1 mutant mice

Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2

A differentially methylated region within the gene Kcnq1 functions as an imprinted promoter and silencer

MicroRNA-153 targeting of KCNQ4 contributes to vascular dysfunction in hypertension

Enhancers compete with a long non-coding RNA for regulation of the Kcnq1 domain


More Like This

Show all results sharing this subject:

  • Chemistry


Show Summary Details

Quick Reference

abbr. for voltage‐gated K+ channel.

Subjects: Chemistry.

Reference entries

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.