Citations for
1KCNQ2, KCNQ3
Novel role of KCNQ2/3 channels in regulating neuronal cell viability.
Zhou X, Wei J, Song M, Francis K, Yu SP.
Cell Death Differ 18(3):493-505. Epub 2010 Oct 1. 2011
2KCNQ2, KCNQ3, KCNQ5
Functional significance of axonal Kv7 channels in hippocampal pyramidal neurons.
Shah MM, Migliore M, Valencia I, Cooper EC, Brown DA.
Proc Natl Acad Sci U S A 105(22):7869-74. Epub 2008 May 30. 2008
3KCNQ1, KCNQ3, KCNQ5
Multiple KCNQ potassium channel subtypes mediate basal anion secretion from the human airway epithelial cell line Calu-3.
Moser SL, Harron SA, Crack J, Fawcett JP, Cowley EA.
J Membr Biol 221(3):153-63. Epub 2008 Feb 9.PMID: 18264812 2008
4EBN1, EBN2, KCNQ2, KCNQ3
Developmental changes in KCNQ2 and KCNQ3 expression in human brain: possible contribution to the age-dependent etiology of benign familial neonatal convulsions.
Kanaumi T, Takashima S, Iwasaki H, Itoh M, Mitsudome A, Hirose S.
Brain Dev 30(5):362-9. Epub 2007 Dec 31.PMID: 18166285 2008
5KCNQ2, KCNQ3
KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes.
Neubauer BA, Waldegger S, Heinzinger J, Hahn A, Kurlemann G, Fiedler B, Eberhard F, Muhle H, Stephani U, Garkisch S, Eeg-Olofsson O, Müller U, Sander T.
Neurology 71(3):177-83.PMID: 18625963 2008
6KCNQ2, KCNQ3, EBN1
Decreased subunit stability as a novel mechanism for potassium current impairment by a KCNQ2 C terminus mutation causing benign familial neonatal convulsions.
Soldovieri MV, Castaldo P, Iodice L, Miceli F, Barrese V, Bellini G, Miraglia del Giudice E, Pascotto A, Bonatti S, Annunziato L, Taglialatela M.
J Biol Chem 281(1):418-28. Epub 2005 Oct 31. 2006
7EJM2, KCNQ3
Genetic association analysis of KCNQ3 and juvenile myoclonic epilepsy in a South Indian population.
Vijai J, Kapoor A, Ravishankar HM, Cherian PJ, Girija AS, Rajendran B, Rangan G, Jayalakshmi S, Mohandas S, Radhakrishnan K, Anand A.
Hum Genet 113(5):461-3. Epub 2003 Aug 20. 2003
8EBN1, EBN2, KCNQ2, KCNQ3
KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum.
Singh NA, Westenskow P, Charlier C, Pappas C, Leslie J, Dillon J, Anderson VE, Sanguinetti MC, Leppert MF; BFNC Physician Consortium.
Brain 126(Pt 12):2726-37. Epub 2003 Oct 8. 2003
9EBN1, EBN2, KCNQ2, KCNQ3
Benign familial neonatal convulsions caused by altered gating of KCNQ2/KCNQ3 potassium channels.
Castaldo P, del Giudice EM, Coppola G, Pascotto A, Annunziato L, Taglialatela M.
J Neurosci 22(2):RC199. 2002
10KCNQ2, KCNQ3
Colocalization and coassembly of two human brain M-type potassium channel subunits that are mutated in epilepsy.
Cooper EC, Aldape KD, Abosch A, Barbaro NM, Berger MS, Peacock WS, Jan YN, Jan LY.
Proc Natl Acad Sci U S A 97(9):4914-9. 2000
11KCNQ2, KCNQ3
KCNQ2/KCNQ3 K+ channels and the molecular pathogenesis of epilepsy: implications for therapy.
Rogawski MA.
Trends Neurosci 23(9):393-8. Review. 2000
12KCNQ2, KCNQ3
Two types of K(+) channel subunit, Erg1 and KCNQ2/3, contribute to the M-like current in a mammalian neuronal cell.
Selyanko AA, Hadley JK, Wood IC, Abogadie FC, Delmas P, Buckley NJ, London B, Brown DA.
J Neurosci 19(18):7742-56 1999
13EBN2, KCNQ3
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.
Charlier C, Singh NA, Ryan SG, Lewis TB, Reus BE, Leach RJ, Leppert M.
Nat Genet 18(1):53-5. 1998
14EBN1, EBN2, KCNQ2, KCNQ3
Functional expression of two KvLQT1-related potassium channels responsible for an inherited idiopathic epilepsy.
Yang WP, Levesque PC, Little WA, Conder ML, Ramakrishnan P, Neubauer MG, Blanar MA.
J Biol Chem 273 : 19419-19423. 1998
15KCNQ2, KCNQ3
KCNQ2 and KCNQ3 potassium channel subunits : molecular correlates of the M-channel.
Wang HS, et al.
Science 282 : 1890-1893. 1998
16EBN1, EBN2, KCNQ2, KCNQ3
Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy.
Schroeder BC, et al.
Nature 396 : 687-690. 1998
17KCNQ2, KCNQ3
The KCNQ2 potassium channel : splice variants, functional and developmental expression. Brain Localization and comparison with KCNQ3.
Tinel N, Lauritzen I, Chouabe C, Lazdunski M, Borsotto M.
FEBS Lett 438 : 171-176. 1998