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Results: 1 to 20 of 192

Similar articles for PubMed (Select 18824591)

1.

Gating pore currents in DIIS4 mutations of NaV1.4 associated with periodic paralysis: saturation of ion flux and implications for disease pathogenesis.

Struyk AF, Markin VS, Francis D, Cannon SC.

J Gen Physiol. 2008 Oct;132(4):447-64. doi: 10.1085/jgp.200809967.

2.

Hypokalemic periodic paralysis: an omega pore mutation affects inactivation.

Männikkö R, Kullmann DM.

Channels (Austin). 2015 Jun 17:0. [Epub ahead of print] No abstract available.

PMID:
26083144
3.

Gating pore currents, a new pathological mechanism underlying cardiac arrhythmias associated with dilated cardiomyopathy.

Moreau A, Gosselin-Badaroudine P, Chahine M.

Channels (Austin). 2015 May 4;9(3):139-44. doi: 10.1080/19336950.2015.1031937.

PMID:
26046592
4.

Gating mechanisms of voltage-gated proton channels.

Okamura Y, Fujiwara Y, Sakata S.

Annu Rev Biochem. 2015 Jun 2;84:685-709. doi: 10.1146/annurev-biochem-060614-034307.

PMID:
26034892
5.

Gating pore current is a novel biophysical defect of Nav1.5 mutations associated with unusual cardiac arrhythmias and dilation.

Chahine M.

Future Cardiol. 2015 May;11(3):287-91. doi: 10.2217/fca.15.23. No abstract available.

PMID:
26021634
6.

Direct estimation of CaV1.2 gating parameters: quantification of voltage sensor - pore transductions and their modulation by FLP 64176.

Beyl S, Kugler P, Timin E, Hering S.

Curr Mol Pharmacol. 2015 May 6. [Epub ahead of print]

PMID:
25966699
7.

Idiopathic generalized epilepsy and hypokalemic periodic paralysis in a family of South Indian descent.

Subramanian M, Senthil N, Sujatha S.

Case Rep Neurol Med. 2015;2015:906049. doi: 10.1155/2015/906049. Epub 2015 Mar 26.

8.

Channelopathies of skeletal muscle excitability.

Cannon SC.

Compr Physiol. 2015 Apr;5(2):761-90. doi: 10.1002/cphy.c140062.

PMID:
25880512
9.

Charging a capacitor from an external fluctuating potential using a single conical nanopore.

Gomez V, Ramirez P, Cervera J, Nasir S, Ali M, Ensinger W, Mafe S.

Sci Rep. 2015 Apr 1;5:9501. doi: 10.1038/srep09501.

10.

Breaking the hydrophobicity of the MscL pore: insights into a charge-induced gating mechanism.

Chandramouli B, Di Maio D, Mancini G, Barone V, Brancato G.

PLoS One. 2015 Mar 31;10(3):e0120196. doi: 10.1371/journal.pone.0120196. eCollection 2015.

11.

Asp-linked glycosylation contributes to surface expression and voltage-dependent gating of Cav1.2 Ca2+ channel.

Park HJ, Min SH, Won YJ, Lee JH.

J Microbiol Biotechnol. 2015 Mar 31. [Epub ahead of print]

12.

The Domain II S4-S5 Linker in Nav1.9: A Missense Mutation Enhances Activation, Impairs Fast Inactivation, and Produces Human Painful Neuropathy.

Han C, Yang Y, de Greef BT, Hoeijmakers JG, Gerrits MM, Verhamme C, Qu J, Lauria G, Merkies IS, Faber CG, Dib-Hajj SD, Waxman SG.

Neuromolecular Med. 2015 Jun;17(2):158-69. doi: 10.1007/s12017-015-8347-9. Epub 2015 Mar 20.

PMID:
25791876
13.

A Model of Electrostimulation Based on the Membrane Capacitance as Electromechanical Transducer for Pore Gating.

Irnich W, Kroll MW.

Pacing Clin Electrophysiol. 2015 Jul;38(7):831-45. doi: 10.1111/pace.12573. Epub 2015 Feb 14.

PMID:
25684121
14.

Rectification of Ion Current in Nanopores Depends on the Type of Monovalent Cations: Experiments and Modeling.

Gamble T, Decker K, Plett TS, Pevarnik M, Pietschmann JF, Vlassiouk I, Aksimentiev A, Siwy ZS.

J Phys Chem C Nanomater Interfaces. 2014 May 8;118(18):9809-9819. Epub 2014 Apr 14.

15.

Gating pore currents are defects in common with two Nav1.5 mutations in patients with mixed arrhythmias and dilated cardiomyopathy.

Moreau A, Gosselin-Badaroudine P, Delemotte L, Klein ML, Chahine M.

J Gen Physiol. 2015 Feb;145(2):93-106. doi: 10.1085/jgp.201411304.

PMID:
25624448
16.

Classification of 2-pore domain potassium channels based on rectification under quasi-physiological ionic conditions.

Chen H, Zuo D, Zhang J, Zhou M, Ma L.

Channels (Austin). 2014;8(6):503-8. doi: 10.4161/19336950.2014.973779.

PMID:
25616686
17.
18.

Erythromelalgia mutation Q875E Stabilizes the activated state of sodium channel Nav1.7.

Stadler T, O'Reilly AO, Lampert A.

J Biol Chem. 2015 Mar 6;290(10):6316-25. doi: 10.1074/jbc.M114.605899. Epub 2015 Jan 9.

PMID:
25575597
19.

Domain III S4 in closed-state fast inactivation: insights from a periodic paralysis mutation.

Groome JR, Jurkat-Rott K, Lehmann-Horn F.

Channels (Austin). 2014;8(5):467-71. doi: 10.4161/19336950.2014.958924.

PMID:
25483590
20.

Human slack potassium channel mutations increase positive cooperativity between individual channels.

Kim GE, Kronengold J, Barcia G, Quraishi IH, Martin HC, Blair E, Taylor JC, Dulac O, Colleaux L, Nabbout R, Kaczmarek LK.

Cell Rep. 2014 Dec 11;9(5):1661-72. doi: 10.1016/j.celrep.2014.11.015. Epub 2014 Dec 4.

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