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Title:	Inactivation of muscle chloride channel by transposon insertion in myotonic mice
Source:	Nature [0028-0836] Steinmeyer, Klaus yr:1991

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description	1.	Jentsch, T J J. "The skeletal muscle chloride channel in dominant and recessive human myotonia." Science 257.5071: 797-800.
description	2.	Lehmann-Horn, F. "Membrane changes in cells from myotonia patients." Physiological reviews 65.2 (1985): 310-56.
description	3.	Fisher, C M. "Dr. Raymond Delacy Adams (1911-2008): an appreciation." The Neurologist 16.3 (2010): 141-142.
description	4.	Lipicky, R J. "Sodium, potassium, and chloride fluxes in intercostal muscle from normal goats and goats with hereditary myotonia." The Journal of general physiology 50.1 (1966): 89-111.
description	5.	Ladd, Myrna G N. "Dynamic balance between activation and repression regulates pre-mRNA alternative splicing during heart development." Developmental dynamics 233.3 (2005): 783-793.
description	6.	Pusch, M. "Myotonia caused by mutations in the muscle chloride channel gene CLCN1." Human mutation 19.4 (2002): 423-34.
description	7.	Shelbourne, P. "Unstable DNA may be responsible for the incomplete penetrance of the myotonic dystrophy phenotype." Human molecular genetics 1.7 (1992): 467-73.
description	8.	Kubisch, C. "ClC-1 chloride channel mutations in myotonia congenita: variable penetrance of mutations shifting the voltage dependence." Human Molecular Genetics 7.11 (1998): 1753-60.
description	9.	Jentsch, Thomas J J. "Molecular structure and physiological function of chloride channels." Physiological reviews 82.2 (2002): 503-568.
description	10.	George, A L L. "Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita)." Nature genetics 3.4: 305-310.
description	11.	Ho, Thai H H. "Transgenic mice expressing CUG-BP1 reproduce splicing mis-regulation observed in myotonic dystrophy." Human Molecular Genetics 14.11 (2005): 1539-47.
description	12.	Cooper, Thomas A A. "Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing." Molecular cell 10.1 (2002): 45-53.
description	13.	Arnyi, Z. "Miller Fisher syndrome: brief overview and update with a focus on electrophysiological findings." European journal of neurology 19.1 (2011): 15-20.
description	14.	Peeples, E. "Familial Miller Fisher Syndrome." Journal of Child Neurology 26.5 (2011): 645-648.
description	15.	Cooper, Thomas A A. "Alternative splicing regulation impacts heart development." Cell 120.1 (2005): 1-2.
description	16.	Atkinson, J. "Myotonia congenita: a histochemical and ultrastructural study in the goat: comparison with abnormalities found in human myotonia dystrophica." The American journal of pathology 102.3 (1981): 324-335.
description	17.	Hoffman, E P P. "Voltage-gated ion channelopathies: inherited disorders caused by abnormal sodium, chloride, and calcium regulation in skeletal muscle." Annual review of medicine 46.1 (1995): 431-41.
description	18.	Conte-Camerino, S H H. "Chloride channel regulation in the skeletal muscle of normal and myotonic goats." Pflügers Archiv 417.6 (1991): 605-10.
description	19.	Rüdel, R. "Molecular pathophysiology of voltage-gated ion channels." Reviews of physiology, biochemistry and pharmacology (1996): 195-268.
description	20.	Bretag, A H H. "Muscle chloride channels." Physiological reviews 67.2 (1987): 618-724.