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FEBS Letters|July 12, 1993
A molecular basis for gating mode transitions in human skeletal muscle Na+ channelsP B Bennett, N Makita, A L GeorgeCirculation Research|February 1, 1996
Multiple domains contribute to the distinct inactivation properties of human heart and skeletal muscle Na+ channelsN Makita, P B Bennett, A L GeorgeBiophysical Journal|January 1, 1996
Comparison of heterologously expressed human cardiac and skeletal muscle sodium channelsD W Wang, A L George, P B BennettProceedings of the National Academy of Sciences of the United States of America|June 11, 1992
Molecular cloning of an atypical voltage-gated sodium channel expressed in human heart and uterus: evidence for a distinct gene familyA L George, T J Knittle, M M TamkunPflugers Archiv : European Journal of Physiology|January 1, 1997
Probing the major skeletal muscle chloride channel with Zn2+ and other sulfhydryl-reactive compoundsL Kürz, S Wagner, A L George, et al.Arthritis and Rheumatism|May 1, 1985
Blastomycosis presenting as monoarticular arthritis. The role of synovial fluid cytologyA L George, J T Hays, B S GrahamJournal of Cardiovascular Electrophysiology|November 1, 1995
Recent advances in understanding the molecular mechanisms of the long QT syndromeD M Roden, A L George, P B BennettThe Journal of Physiology|July 14, 1998
Human sodium channel gating defects caused by missense mutations in S6 segments associated with myotonia: S804F and V1293ID S Green, A L George, S C CannonVeterinary Immunology and Immunopathology|July 1, 1989
Chemotactic response of bovine neutrophils to Pasteurella haemolytica culture fluidC J Brunner, A L George, C L HsuThe Journal of General Physiology|February 1, 1996
Paramyotonia congenita mutations reveal different roles for segments S3 and S4 of domain D4 in hSkM1 sodium channel gatingS Ji, A L George, R Horn, et al.Pageof 12