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