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t/gene-kcnq1

KCNQ1 gene

Discuss publications and research concerning the KCNQ1 gene.

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Related literature

Derivation of an induced pluripotent stem cell line from a long QT syndrome type 1 patient with a pathogenic KCNQ1 c.1552C > T (p.Arg518Ter) variant.
KCNQ1
[A study of parent-of-origin effect of single nucleotide polymorphisms of imprinted gene KCNQ1 on risk for hypertension].
KCNQ1
Bridging local-global transmembrane protein contexts with contrastive pretraining for alignment-free pathogenicity prediction.
KCNQ1
Monogenic Syndromes as a Cause of Adverse Drug Reactions in the Russian Population.
KCNQ1
Chemical tuning reveals a cation-π gating bridge between the voltage-sensor and pore domains in the Kv7.1 potassium channel.
KCNQ1
Protein Language Models and Structure-Based Machine Learning for Prediction of Allosteric Binding Sites in Protein Kinases: An Explainable AI Framework Grounded in Energy Landscape-Encoded Frustration
KCNQ1
Functional Profiling of KCNE1 Variants Informs Population Carrier Frequency of Jervell and Lange-Nielsen Syndrome Type 2.
KCNQ1
Molecular mechanisms of function deficiencies in KCNQ1 variants associated with Jervell and Lange-Nielsen syndrome.
KCNQ1
Graded activation of mutant K41C-KCNE1:KCNQ1 channel complexes by mefenamic acid.
KCNQ1
Deep Learning-Augmented ECG Analysis for Screening and Genotype Prediction of Congenital Long QT Syndrome.
KCNQ1

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