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KCNQ3 gene

Known as: Kv7.3, POTASSIUM CHANNEL, VOLTAGE-GATED, KQT-LIKE SUBFAMILY, MEMBER 3, potassium voltage-gated channel subfamily Q member 3 
National Institutes of Health

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KCNQ3 Potassium Channel

Papers overview

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2015
2015
Differential Nav and KCNQ2/3 channel binding to Ankyrin-G 1 An Ankyrin-G N-terminal gate and casein kinase 2 dually regulate binding of voltage-gated sodium and KCNQ2/3 potassium channels
In many mammalian neurons, fidelity and robustness of action potential generation and conduction depends on the co-localization… 
2014
2014
Anovel KCNQ 3 mutation in familial epilepsy with focal seizures and intellectual disability
Mutations in the KCNQ2 gene encoding for voltage-gated potassium channel subunits have been found in patients affected with early… 
2011
2011
Phenotype and Genotype Relationship between Inherited Cardiac Arrhythmia and Epileptic Syndrome
Inherited channel disorders are associated with paroxysmal dysfunction of excitable tissues and manifest as diseases of the heart… 
2011
2011
Rolando-Epilepsie
ZusammenfassungDie Rolando-Epilepsie (RE) gehört zu den häufigsten Epilepsiesyndromen des Kindesalters. Charakteristisch sind… 
2010
2010
Molecular mechanisms in the epilepsies of infancy.
Over the past decade and a half, considerable advances have been made in the understanding of the molecular mechanisms underlying… 
2009
2009
Untersuchung der physiologischen Rolle von Kv7.2-Kanälen und der pathophysiologischen Mechanismen von Kv7.2-Kanaldefizienz im Gehirn der Maus (Mus musculus, Linnaeus 1758)
  • Vu Le
  • 2009
  • Corpus ID: 94221697
Mutationen in den humanen KCNQ2- und KCNQ3-Genen, welche fur M-Kanaluntereinheiten (Kv7.2 und Kv7.3) kodieren, sind mit einer… 
2004
2004
Novel mutations in the KCNQ 2 gene link epilepsy to a dysfunction of the KCNQ 2-calmodulin interaction
M utations in the voltage gated potassium channels KCNQ2 (OMIM 602235) and KCNQ3 (OMIM 602232) are associated with an autosomal… 
2004
2004
Molecular KCNQ 2 Is a Nodal K Channel
Mutations in the gene encoding the K channel KCNQ2 cause neonatal epilepsy and myokymia, indicating that KCNQ2 regulates the… 
2003
2003
Genetic association analysis of KCNQ3 and juvenile myoclonic epilepsy
Juvenile myoclonic epilepsy (JME) is a common subtype of idiopathic generalized epilepsy that shows a complex pattern of… 
2003
2003
Potassium Channels by Extracellular Protons
Changes in extracellular pH occur during both physiological neuronal activity and pathological conditions such as epilepsy and…