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The Journal of Biological Chemistry|October 18, 2000
Residues lining the inner pore vestibule of human muscle chloride channelsC Fahlke, R R Desai, N Gillani, et al.Nature|August 24, 1995
Molecular mechanism for an inherited cardiac arrhythmiaP B Bennett, K Yazawa, N Makita, et al.Neuroreport|October 23, 1995
Paramyotonia congenita without paralysis on exposure to cold: a novel mutation in the SCN4A gene (Val1293Ile)M C Koch, K Baumbach, A L George, et al.Pflugers Archiv : European Journal of Physiology|May 1, 1994
Functional expression and properties of the human skeletal muscle sodium channelM Chahine, P B Bennett, A L George, et al.Human Molecular Genetics|August 1, 1995
Myotonia levior is a chloride channel disorderF Lehmann-Horn, V Mailänder, R Heine, et al.Biophysical Journal|August 31, 1999
Structural determinants of slow inactivation in human cardiac and skeletal muscle sodium channelsY Y Vilin, N Makita, A L George, et al.Neuron|August 1, 1995
An aspartic acid residue important for voltage-dependent gating of human muscle chloride channelsC Fahlke, R Rüdel, N Mitrovic, et al.Biophysical Journal|August 1, 1996
Mechanism of voltage-dependent gating in skeletal muscle chloride channelsC Fahlke, A Rosenbohm, N Mitrovic, et al.Annals of Neurology|February 11, 1992
Primary structure of the adult human skeletal muscle voltage-dependent sodium channelA L George, J Komisarof, R G Kallen, et al.Current Biology : CB|August 23, 2001
From stones to bones: the biology of ClC chloride channelsA L George, L Bianchi, E M Link, et al.Pageof 12