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Items: 1 to 20 of 34


Sodium channel biophysics, late sodium current and genetic arrhythmic syndromes.

Chadda KR, Jeevaratnam K, Lei M, Huang CL.

Pflugers Arch. 2017 Jun;469(5-6):629-641. doi: 10.1007/s00424-017-1959-1. Epub 2017 Mar 6. Review.


Sequence CLCN1 and SCN4A in patients with Nondystrophic myotonias in Chinese populations: Genetic and pedigree analysis of 10 families and review of the literature.

Yang X, Jia H, An R, Xi J, Xu Y.

Channels (Austin). 2017 Jan 2;11(1):55-65. doi: 10.1080/19336950.2016.1212140. Epub 2016 Jul 14.


Mice with an NaV1.4 sodium channel null allele have latent myasthenia, without susceptibility to periodic paralysis.

Wu F, Mi W, Fu Y, Struyk A, Cannon SC.

Brain. 2016 Jun;139(Pt 6):1688-99. doi: 10.1093/brain/aww070. Epub 2016 Apr 5.


Genetic neurological channelopathies: molecular genetics and clinical phenotypes.

Spillane J, Kullmann DM, Hanna MG.

J Neurol Neurosurg Psychiatry. 2016 Jan;87(1):37-48. doi: 10.1136/jnnp-2015-311233. Epub 2015 Nov 11. Review.


Channelopathies of skeletal muscle excitability.

Cannon SC.

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


Sodium channel slow inactivation as a therapeutic target for myotonia congenita.

Novak KR, Norman J, Mitchell JR, Pinter MJ, Rich MM.

Ann Neurol. 2015 Feb;77(2):320-32. doi: 10.1002/ana.24331. Epub 2015 Jan 9.


Bumetanide prevents transient decreases in muscle force in murine hypokalemic periodic paralysis.

Wu F, Mi W, Cannon SC.

Neurology. 2013 Mar 19;80(12):1110-6. doi: 10.1212/WNL.0b013e3182886a0e. Epub 2013 Feb 20.


Biophysical characterization of M1476I, a sodium channel founder mutation associated with cold-induced myotonia in French Canadians.

Zhao J, Duprè N, Puymirat J, Chahine M.

J Physiol. 2012 Jun 1;590(11):2629-44. doi: 10.1113/jphysiol.2011.223461. Epub 2012 Jan 16.


Skeletal muscle na channel disorders.

Simkin D, Bendahhou S.

Front Pharmacol. 2011 Oct 14;2:63. doi: 10.3389/fphar.2011.00063. eCollection 2011.


Relationships between resting conductances, excitability, and t-system ionic homeostasis in skeletal muscle.

Fraser JA, Huang CL, Pedersen TH.

J Gen Physiol. 2011 Jul;138(1):95-116. doi: 10.1085/jgp.201110617. Epub 2011 Jun 13.


History dependence of human muscle-fiber conduction velocity during voluntary isometric contractions.

McGill KC, Lateva ZC.

J Appl Physiol (1985). 2011 Sep;111(3):630-41. doi: 10.1152/japplphysiol.00208.2011. Epub 2011 May 12.


A mutation in a rare type of intron in a sodium-channel gene results in aberrant splicing and causes myotonia.

Kubota T, Roca X, Kimura T, Kokunai Y, Nishino I, Sakoda S, Krainer AR, Takahashi MP.

Hum Mutat. 2011 Jul;32(7):773-82. doi: 10.1002/humu.21501. Epub 2011 Apr 28.


Open- and closed-state fast inactivation in sodium channels: differential effects of a site-3 anemone toxin.

Groome J, Lehmann-Horn F, Holzherr B.

Channels (Austin). 2011 Jan-Feb;5(1):65-78. Epub 2011 Jan 1.


Sarcolemmal-restricted localization of functional ClC-1 channels in mouse skeletal muscle.

Lueck JD, Rossi AE, Thornton CA, Campbell KP, Dirksen RT.

J Gen Physiol. 2010 Dec;136(6):597-613. doi: 10.1085/jgp.201010526. Epub 2010 Nov 15.


Sodium channelopathies of skeletal muscle result from gain or loss of function.

Jurkat-Rott K, Holzherr B, Fauler M, Lehmann-Horn F.

Pflugers Arch. 2010 Jul;460(2):239-48. doi: 10.1007/s00424-010-0814-4. Epub 2010 Mar 17. Review.


Voltage-sensor mutations in channelopathies of skeletal muscle.

Cannon SC.

J Physiol. 2010 Jun 1;588(Pt 11):1887-95. doi: 10.1113/jphysiol.2010.186874. Epub 2010 Feb 15. Review.


A novel method to quantify contribution of channels and transporters to membrane potential dynamics.

Cha CY, Himeno Y, Shimayoshi T, Amano A, Noma A.

Biophys J. 2009 Dec 16;97(12):3086-94. doi: 10.1016/j.bpj.2009.08.060.


Targeted mutation of mouse skeletal muscle sodium channel produces myotonia and potassium-sensitive weakness.

Hayward LJ, Kim JS, Lee MY, Zhou H, Kim JW, Misra K, Salajegheh M, Wu FF, Matsuda C, Reid V, Cros D, Hoffman EP, Renaud JM, Cannon SC, Brown RH Jr.

J Clin Invest. 2008 Apr;118(4):1437-49. doi: 10.1172/JCI32638.


Cold-induced defects of sodium channel gating in atypical periodic paralysis plus myotonia.

Webb J, Cannon SC.

Neurology. 2008 Mar 4;70(10):755-61. Epub 2007 Sep 26.


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