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The Journal of Physiology|January 10, 1998
Role in fast inactivation of the IV/S4-S5 loop of the human muscle Na+ channel probed by cysteine mutagenesisH Lerche, W Peter, R Fleischhauer, et al.Neuromuscular Disorders : NMD|January 1, 1991
Altered sodium channel behaviour causes myotonia in dominantly inherited myotonia congenitaP A Iaizzo, C Franke, H Hatt, et al.The Biochemical Journal|October 15, 1996
Calmodulin sensitivity of the sarcoplasmic reticulum ryanodine receptor from normal and malignant-hyperthermia-susceptible muscleS O'Driscoll, T V McCarthy, H M Eichinger, et al.British Journal of Anaesthesia|March 4, 2000
Malignant hyperthermia causing Gly2435Arg mutation of the ryanodine receptor facilitates ryanodine-induced calcium release in myotubesH Brinkmeier, J Krämer, R Krämer, et al.The Journal of Biological Chemistry|April 17, 1999
Identification of three cysteines as targets for the Zn2+ blockade of the human skeletal muscle chloride channelL L Kürz, H Klink, I Jakob, et al.Muscle & Nerve|September 1, 1981
Clinical study of paramyotonia congenita with and without myotonia in a warm environmentA Haass, K Ricker, R Rüdel, et al.Molecular Pharmacology|December 1, 1996
Activation of the skeletal muscle ryanodine receptor by suramin and suramin analogsM Hohenegger, M Matyash, K Poussu, et al.Neurology|August 1, 1994
Proximal myotonic myopathy: a new dominant disorder with myotonia, muscle weakness, and cataractsK Ricker, M C Koch, F Lehmann-Horn, et al.Maturitas|October 1, 1994
The prevalence of symptoms in menopausal women in the Far East: Singapore segmentT McCarthyPageof 56