Format
Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 1 to 20 of 199

1.

MrgD activation inhibits KCNQ/M-currents and contributes to enhanced neuronal excitability.

Crozier RA, Ajit SK, Kaftan EJ, Pausch MH.

J Neurosci. 2007 Apr 18;27(16):4492-6.

2.

Angiotensin II regulates neuronal excitability via phosphatidylinositol 4,5-bisphosphate-dependent modulation of Kv7 (M-type) K+ channels.

Zaika O, Lara LS, Gamper N, Hilgemann DW, Jaffe DB, Shapiro MS.

J Physiol. 2006 Aug 15;575(Pt 1):49-67. Epub 2006 Jun 15.

3.

Reconstitution of muscarinic modulation of the KCNQ2/KCNQ3 K(+) channels that underlie the neuronal M current.

Shapiro MS, Roche JP, Kaftan EJ, Cruzblanca H, Mackie K, Hille B.

J Neurosci. 2000 Mar 1;20(5):1710-21.

4.
5.

Subunit-specific modulation of KCNQ potassium channels by Src tyrosine kinase.

Gamper N, Stockand JD, Shapiro MS.

J Neurosci. 2003 Jan 1;23(1):84-95.

6.

Stoichiometry of expressed KCNQ2/KCNQ3 potassium channels and subunit composition of native ganglionic M channels deduced from block by tetraethylammonium.

Hadley JK, Passmore GM, Tatulian L, Al-Qatari M, Ye F, Wickenden AD, Brown DA.

J Neurosci. 2003 Jun 15;23(12):5012-9.

8.

PIP(2) activates KCNQ channels, and its hydrolysis underlies receptor-mediated inhibition of M currents.

Zhang H, Craciun LC, Mirshahi T, Rohács T, Lopes CM, Jin T, Logothetis DE.

Neuron. 2003 Mar 27;37(6):963-75.

9.
10.

Cholinergic suppression of KCNQ channel currents enhances excitability of striatal medium spiny neurons.

Shen W, Hamilton SE, Nathanson NM, Surmeier DJ.

J Neurosci. 2005 Aug 10;25(32):7449-58.

11.

Suppression of KCNQ/M (Kv7) potassium channels in dorsal root ganglion neurons contributes to the development of bone cancer pain in a rat model.

Zheng Q, Fang D, Liu M, Cai J, Wan Y, Han JS, Xing GG.

Pain. 2013 Mar;154(3):434-48. doi: 10.1016/j.pain.2012.12.005. Epub 2012 Dec 20.

PMID:
23352759
12.

Activation of KCNQ2/3 potassium channels by novel pyrazolo[1,5-a]pyrimidin-7(4H)-one derivatives.

Jia C, Qi J, Zhang F, Mi Y, Zhang X, Chen X, Liu L, Du X, Zhang H.

Pharmacology. 2011;87(5-6):297-310. doi: 10.1159/000327384. Epub 2011 May 17.

PMID:
21577044
13.

N-(6-chloro-pyridin-3-yl)-3,4-difluoro-benzamide (ICA-27243): a novel, selective KCNQ2/Q3 potassium channel activator.

Wickenden AD, Krajewski JL, London B, Wagoner PK, Wilson WA, Clark S, Roeloffs R, McNaughton-Smith G, Rigdon GC.

Mol Pharmacol. 2008 Mar;73(3):977-86. Epub 2007 Dec 18.

14.
15.
17.

Modulation of K(v)7 potassium channels by a novel opener pyrazolo[1,5-a]pyrimidin-7(4H)-one compound QO-58.

Zhang F, Mi Y, Qi JL, Li JW, Si M, Guan BC, Du XN, An HL, Zhang HL.

Br J Pharmacol. 2013 Feb;168(4):1030-42. doi: 10.1111/j.1476-5381.2012.02232.x.

18.

Sphingosine-1-phosphate via activation of a G-protein-coupled receptor(s) enhances the excitability of rat sensory neurons.

Zhang YH, Fehrenbacher JC, Vasko MR, Nicol GD.

J Neurophysiol. 2006 Sep;96(3):1042-52. Epub 2006 May 24.

19.

Pre- and postsynaptic activation of M-channels by a novel opener dampens neuronal firing and transmitter release.

Peretz A, Sheinin A, Yue C, Degani-Katzav N, Gibor G, Nachman R, Gopin A, Tam E, Shabat D, Yaari Y, Attali B.

J Neurophysiol. 2007 Jan;97(1):283-95. Epub 2006 Oct 18.

20.

Expression of a calmodulin-binding KCNQ2 potassium channel fragment modulates neuronal M-current and membrane excitability.

Shahidullah M, Santarelli LC, Wen H, Levitan IB.

Proc Natl Acad Sci U S A. 2005 Nov 8;102(45):16454-9. Epub 2005 Nov 1.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk