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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   18 Cited 18 times in Scopus18 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 78   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 56   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 82   38 Cited 45 times in Scopus45 0