Alternative splicing of KCNQ2 potassium channel transcripts contributes to the functional diversity of M-currents
David Brown
The Journal of Physiology, 2001
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The genomic basis of KV3.4 potassium channel mRNA diversity in mice
Harald H Jockusch
Gene, 2001
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Localization of Two Potassium Channel β Subunit Genes, KCNA1B and KCNA2B
Mathew Thayer
Genomics, 1996
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Human TREK2, a 2P domain mechano-sensitive K+ channel with multiple regulations by polyunsaturated fatty acids, lysophospholipids, and G(s), G(i), and G(q) protein-coupled receptors
Florian Lesage
Journal of Biological Chemistry, 2000
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Evolutionary analyses of KCNQ1 and HERG voltage-gated potassium channel sequences reveal location-specific susceptibility and augmented chemical severities of arrhythmogenic mutations
Eric Accili
BMC evolutionary biology, 2008
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Gene Structures and Expression Profiles of Three Human KCND (Kv4) Potassium Channels Mediating A-Type Currents ITO and ISA
Ulrich Luhmann, Xin-ran Zhu
Genomics, 2000
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KCNQ2 and KCNQ3 Potassium Channel Subunits: Molecular Correlates of the M-Channel
R. Wymore
Science
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The KCNQ2 potassium channel: splice variants, functional and developmental expression. Brain localization and comparison with KCNQ3
Michel Lazdunski
FEBS Letters, 1998
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Surface Expression and Single Channel Properties of KCNQ2/KCNQ3, M-type K+ Channels Involved in Epilepsy
Thomas Jentsch
Journal of Biological Chemistry, 2000
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Shaw-like rat brain potassium channel cDNA's with divergent 3′ ends
Jacinta Williams
FEBS Letters, 1991
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Germ-line mutation of KCNQ2, p.R213W, in a Japanese family with benign familial neonatal convulsion
Teguh Haryo Sasongko
Pediatrics International, 2008
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Loss-of-Function and Gain-of-Function Mutations in KCNQ5 Cause Intellectual Disability or Epileptic Encephalopathy
Grazia Mancini
American journal of human genetics, 2017
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Influence of rs1800172 common gene variation on the structure and function of potassium voltage-gated channel subfamily Q member 1
Central Asian Journal of Medical and Pharmaceutical Sciences Innovation (CAJMPSI)
Central Asian Scientific Press (CAS-Press), 2022
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Biophysical and biomedical aspects of KCNE potassium channel ancillary subunits
Leonardo Hernandez
2004
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Molecular cloning, characterization, and genomic localization of a human potassium channel gene
Gregory Landes
Genomics, 1992
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Chromosomal localization of 15 ion channel genes
Mark C Russell
Somatic Cell and Molecular Genetics, 1996
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Molecular Cloning and Functional Expression of KCNQ5, a Potassium Channel Subunit That May Contribute to Neuronal M-current Diversity*
G Seebohm
2000
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doi:10.1093/nar/gki098 The EMBL Nucleotide Sequence Database
Matias Castro
2004
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Genomic Localization of the Human Gene for KCNA10, a cGMP-Activated K Channel
Gary Desir
Genomics, 1997
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Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC)
P. Piccinelli, Pasqualina Castaldo
Neurogenetics, 2005
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Genomic organization, nucleotide sequence, and cellular distribution of a Shaw-related potassium channel gene, Kv3.3, and mapping of Kv3.3 and Kv3.4 to human chromosomes 19 and 1
L. Salkoff
Genomics, 1992
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Initial isolation and analysis of the human Kv1.7 (KCNA7) gene, a member of the voltage-gated potassium channel gene family
Sergei Kvasha
Gene, 2001
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Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions
Joost Das, Dick Lindhout
Neuroscience Letters, 2009
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Expression profile and characterisation of a truncated KCNQ5 splice variant
Iain Greenwood
Biochemical and Biophysical Research Communications, 2008
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Electrophysiological characterization of three non-synonymous single nucleotide polymorphisms (R87Q, A251T, and P307S) found in hKv1.5
Jean Champagne
Pflügers Archiv - European Journal of Physiology, 2006
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Phylogenomic Analysis and Evolution of the Potassium Channel Gene Family
David Parry-Smith
Receptors & Channels, 2003
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Atypical Gating Of M-Type Potassium Channels Conferred by Mutations in Uncharged Residues in the S4 Region of KCNQ2 Causing Benign Familial Neonatal Convulsions
Francesco Miceli, M. Soldovieri
Journal of Neuroscience, 2007
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Decreased Subunit Stability as a Novel Mechanism for Potassium Current Impairment by a KCNQ2 C Terminus Mutation Causing Benign Familial Neonatal Convulsions
Francesco Miceli, M. Soldovieri
Journal of Biological Chemistry, 2006
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A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions
Алекси Алеков
Annals of Neurology, 1999
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MS#013 Aminoff M Nat Genet 21 309 313 1999
Ralf Krahe
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