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KCNB1 gene

Known as: Kv2.1, POTASSIUM CHANNEL, VOLTAGE-GATED, SHAB-RELATED SUBFAMILY, MEMBER 1, potassium voltage-gated channel subfamily B member 1 
National Institutes of Health

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Related topics

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KCNB2 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
High throughput Characterization of KCNB1 variants Associated with Developmental and Epileptic Encephalopathy
Pathogenic variants in KCNB1, encoding the voltage-gated potassium channel Kv2.1, are associated with developmental and epileptic… 
2019
2019
Haut taux de diagnostic identifié par séquençage de l’exome dans les pathologies neurologiques associant déficience intellectuelle et dystonie
2017
2017
Corrigendum: Novel KCNB1 mutation associated with non-syndromic intellectual disability
Correction to: Journal of Human Genetics doi:10.1038/jhg.2016.154; published online 8 December 2016. Since the advance online… 
2017
2017
Role of KCNB1 in the prognosis of gliomas and autophagy modulation
Increasing evidence suggests that ion channel genes play an important role in the progression of gliomas. However, the mechanisms… 
Review
2017
Review
2017
Clinician ’ s guide to genes associated with Rett-like phenotypes – Investigation of a Danish cohort and review of the literature
This article is protected by copyright. All rights reserved. This article has been accepted for publication and undergone full… 
2016
2016
Oxidation of KCNB 1 Potassium Channels Causes Neurotoxicity and Cognitive Impairment in a Mouse Model of Traumatic Brain Injury
injury (TBT), a condition characterized by extensive oxidative stress. Dasatinib, a Food and Drug Administration—approved… 
2015
2015
Erratum to: Association of KCNB1 polymorphisms with lipid metabolisms and insulin resistance: a case-control design of population-based cross-sectional study in Chinese Han population
2003
2003
Quantitative Analysis of Potassium Channel Gene Expression in Smooth Muscle Cells of Intact Arteries
1 School of Biomedical Sciences, University of Leeds, Great Britain. Correspondence should be addressed to D. J. Beech (e-mail… 
1996
1996
Identification of a Ser857-Asn857 substitution in DRK1 (KCNB1), population frequencies and lack of association to the low voltage alpha EEG trait
Abstract A nonconservative amino acid substitution (Ser857Asn) in the human delayed-rectifier potassium channel DRK1 (KCNB1 locus… 
1995
1995
Thirteen genes (Cebpb, E2f1, Tcf4, Cyp24, Pck1, Acra4, Edn3, Kcnb1, Mc3r, Ntsr, Cd40, Plcg1 and Rcad) that probably lie in the distal imprinting region of mouse chromosome 2 are not monoallelically…
Seven imprinted genes are currently known in the mouse but none have been identified yet in the distal imprinting region of mouse… 
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