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Items: 1 to 20 of 92

1.

Dysfunction of the Heteromeric KV7.3/KV7.5 Potassium Channel is Associated with Autism Spectrum Disorders.

Gilling M, Rasmussen HB, Calloe K, Sequeira AF, Baretto M, Oliveira G, Almeida J, Lauritsen MB, Ullmann R, Boonen SE, Brondum-Nielsen K, Kalscheuer VM, Tümer Z, Vicente AM, Schmitt N, Tommerup N.

Front Genet. 2013 Apr 16;4:54. doi: 10.3389/fgene.2013.00054. eCollection 2013.

2.

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. 2008 Jul 15;71(3):177-83. doi: 10.1212/01.wnl.0000317090.92185.ec.

PMID:
18625963
3.

Neutralization of a negative charge in the S1-S2 region of the KV7.2 (KCNQ2) channel affects voltage-dependent activation in neonatal epilepsy.

Wuttke TV, Penzien J, Fauler M, Seebohm G, Lehmann-Horn F, Lerche H, Jurkat-Rott K.

J Physiol. 2008 Jan 15;586(2):545-55. Epub 2007 Nov 15.

4.

Molecular determinants of KCNQ (Kv7) K+ channel sensitivity to the anticonvulsant retigabine.

Schenzer A, Friedrich T, Pusch M, Saftig P, Jentsch TJ, Grötzinger J, Schwake M.

J Neurosci. 2005 May 18;25(20):5051-60.

5.

Structural determinants of M-type KCNQ (Kv7) K+ channel assembly.

Schwake M, Athanasiadu D, Beimgraben C, Blanz J, Beck C, Jentsch TJ, Saftig P, Friedrich T.

J Neurosci. 2006 Apr 5;26(14):3757-66.

6.

Sodium and potassium channel dysfunctions in rare and common idiopathic epilepsy syndromes.

Hahn A, Neubauer BA.

Brain Dev. 2009 Aug;31(7):515-20. doi: 10.1016/j.braindev.2009.04.012. Epub 2009 May 22. Review.

PMID:
19464834
7.

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. 1998 Jul 31;273(31):19419-23.

8.

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. 2003 Dec;126(Pt 12):2726-37. Epub 2003 Oct 8.

9.

Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy.

Schroeder BC, Kubisch C, Stein V, Jentsch TJ.

Nature. 1998 Dec 17;396(6712):687-90.

PMID:
9872318
10.

The new voltage gated potassium channel KCNQ5 and neonatal convulsions.

Kananura C, Biervert C, Hechenberger M, Engels H, Steinlein OK.

Neuroreport. 2000 Jun 26;11(9):2063-7.

PMID:
10884071
11.

The therapeutic potential of neuronal KCNQ channel modulators.

Gribkoff VK.

Expert Opin Ther Targets. 2003 Dec;7(6):737-48. Review.

PMID:
14640909
12.

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. 2002 Jan 15;22(2):RC199.

13.

A recurrent KCNQ2 pore mutation causing early onset epileptic encephalopathy has a moderate effect on M current but alters subcellular localization of Kv7 channels.

Abidi A, Devaux JJ, Molinari F, Alcaraz G, Michon FX, Sutera-Sardo J, Becq H, Lacoste C, Altuzarra C, Afenjar A, Mignot C, Doummar D, Isidor B, Guyen SN, Colin E, De La Vaissière S, Haye D, Trauffler A, Badens C, Prieur F, Lesca G, Villard L, Milh M, Aniksztejn L.

Neurobiol Dis. 2015 Aug;80:80-92. doi: 10.1016/j.nbd.2015.04.017. Epub 2015 May 22.

PMID:
26007637
14.

Surface expression and single channel properties of KCNQ2/KCNQ3, M-type K+ channels involved in epilepsy.

Schwake M, Pusch M, Kharkovets T, Jentsch TJ.

J Biol Chem. 2000 May 5;275(18):13343-8.

15.

Participation of KCNQ (Kv7) potassium channels in myogenic control of cerebral arterial diameter.

Zhong XZ, Harhun MI, Olesen SP, Ohya S, Moffatt JD, Cole WC, Greenwood IA.

J Physiol. 2010 Sep 1;588(Pt 17):3277-93. doi: 10.1113/jphysiol.2010.192823. Epub 2010 Jul 12.

16.

Kv7 channels can function without constitutive calmodulin tethering.

Gómez-Posada JC, Aivar P, Alberdi A, Alaimo A, Etxeberría A, Fernández-Orth J, Zamalloa T, Roura-Ferrer M, Villace P, Areso P, Casis O, Villarroel A.

PLoS One. 2011;6(9):e25508. doi: 10.1371/journal.pone.0025508. Epub 2011 Sep 28.

17.

Molecular cloning and functional expression of KCNQ5, a potassium channel subunit that may contribute to neuronal M-current diversity.

Lerche C, Scherer CR, Seebohm G, Derst C, Wei AD, Busch AE, Steinmeyer K.

J Biol Chem. 2000 Jul 21;275(29):22395-400.

18.

Distinct subunit contributions to the activation of M-type potassium channels by PI(4,5)P2.

Telezhkin V, Brown DA, Gibb AJ.

J Gen Physiol. 2012 Jul;140(1):41-53. doi: 10.1085/jgp.201210796. Epub 2012 Jun 11.

19.

A pore residue of the KCNQ3 potassium M-channel subunit controls surface expression.

Gómez-Posada JC, Etxeberría A, Roura-Ferrer M, Areso P, Masin M, Murrell-Lagnado RD, Villarroel A.

J Neurosci. 2010 Jul 7;30(27):9316-23. doi: 10.1523/JNEUROSCI.0851-10.2010.

20.

Functional implications of KCNE subunit expression for the Kv7.5 (KCNQ5) channel.

Roura-Ferrer M, Etxebarria A, Solé L, Oliveras A, Comes N, Villarroel A, Felipe A.

Cell Physiol Biochem. 2009;24(5-6):325-34. doi: 10.1159/000257425. Epub 2009 Nov 4.

PMID:
19910673
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