Literature DB >> 12210360

Genetic disorders of neuromuscular ion channels.

Kleopas A Kleopa1, Robert L Barchi.   

Abstract

Ion channels are complex proteins that span the lipid bilayer of the cell membrane, where they orchestrate the electrical signals necessary for normal function of the central nervous system, peripheral nerve, and both skeletal and cardiac muscle. The role of ion channel defects in the pathogenesis of numerous disorders, many of them neuromuscular, has become increasingly apparent over the last decade. Progress in molecular biology has allowed cloning and expression of genes that encode channel proteins, while comparable advances in biophysics, including patch-clamp electrophysiology and related techniques, have made the study of expressed proteins at the level of single channel molecules possible. Understanding the molecular basis of ion channel function and dysfunction will facilitate both the accurate classification of these disorders and the rational development of specific therapeutic interventions. This review encompasses clinical, genetic, and pathophysiological aspects of ion channels disorders, focusing mainly on those with neuromuscular manifestations. Copyright 2002 Wiley Periodicals, Inc.

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Year:  2002        PMID: 12210360     DOI: 10.1002/mus.10164

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  6 in total

1.  The C-terminal domain of ßIV-spectrin is crucial for KCNQ2 aggregation and excitability at nodes of Ranvier.

Authors:  Jérôme J Devaux
Journal:  J Physiol       Date:  2010-10-20       Impact factor: 5.182

2.  Fatigue-inducing stimulation resolves myotonia in a drug-induced model.

Authors:  Erik van Lunteren; Sarah E Spiegler; Michelle Moyer
Journal:  BMC Physiol       Date:  2011-02-28

3.  Autoimmune channelopathies of the nervous system.

Authors:  Kleopas A Kleopa
Journal:  Curr Neuropharmacol       Date:  2011-09       Impact factor: 7.363

4.  Impaired Wheel Running Exercise in CLC-1 Chloride Channel-Deficient Myotonic Mice.

Authors:  Erik van Lunteren; Michelle Moyer; Jessica Cooperrider; Jennifer Pollarine
Journal:  Front Physiol       Date:  2011-08-09       Impact factor: 4.566

5.  The Effects of the KCNQ Openers Retigabine and Flupirtine on Myotonia in Mammalian Skeletal Muscle Induced by a Chloride Channel Blocker.

Authors:  Tzu-Rong Su; Wen-Shan Zei; Ching-Chyuan Su; George Hsiao; Min-Jon Lin
Journal:  Evid Based Complement Alternat Med       Date:  2012-03-25       Impact factor: 2.629

6.  MBNL and CELF proteins regulate alternative splicing of the skeletal muscle chloride channel CLCN1.

Authors:  Yoshihiro Kino; Chika Washizu; Yoko Oma; Hayato Onishi; Yuriko Nezu; Noboru Sasagawa; Nobuyuki Nukina; Shoichi Ishiura
Journal:  Nucleic Acids Res       Date:  2009-08-31       Impact factor: 16.971

  6 in total

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