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Quinlan, Kate G. R., Seto, Jane T., Turner, Nigel, Vandebrouck, Aurelie, Floetenmeyer, Matthias, Macarthur, Daniel G., Raftery, Joanna M., Lek, Monkol, Yang, Nan, Parton, Robert G., Cooney, Gregory J. and North, Kathryn N. (2010) α-Actinin-3 deficiency results in reduced glycogen phosphorylase activity and altered calcium handling in skeletal muscle. Human Molecular Genetics, 19 7: ddq010-1335-ddq010-1346. doi:10.1093/hmg/ddq010 83   19 Cited 20 times in Scopus20 0
Cooper, Sandra T., Kizana, Eddy, Yates, Jonathon D., Lo, Harriet P., Yang, Nan, Wu, Zhan H., Alexander, Ian E. and North, Kathryn N. (2007) Dystrophinopathy carrier determination and detection of protein deficiencies in muscular dystrophy using lentiviral MyoD-forced myogenesis. Neuromuscular disorders, 17 4: 276-284. doi:10.1016/j.nmd.2006.12.010 79   19 Cited 19 times in Scopus19 0
Au, Carol G., Cooper , Sandra T., Lo, Harriet P., Compton, Alison G., Yang, Nan, Wintour, E. Marelyn, North, Kathryn N. and Winlaw, David S. (2004) Expression of Aquaporin 1 in Human Cardiac and Skeletal Muscle. Journal of Molecular and Cellular Cardiology, 36 5: 655-666. doi:10.1016/j.yjmcc.2004.01.009 57   33 Cited 37 times in Scopus37 0
Lo, Harriet P., Cooper, Sandra T., Evesson, Frances J., Seto, Jane T., Chiotis, Maria, Tay, Valerie, Compton, Alison G., Cairns, Anita G., Corbett, Alistair, MacArthur, Daniel G., Yang, Nan, Reardon, Katrina and North, Kathryn N. (2008) Limb–girdle muscular dystrophy: Diagnostic evaluation, frequency and clues to pathogenesis. Neuromuscular Disorders, 18 1: 34-44. doi:10.1016/j.nmd.2007.08.009 83   39 Cited 45 times in Scopus45 0