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Results: 3

Authors: Blair, E Redwood, C Ashrafian, H Oliveira, M Broxholme, J Kerr, B Salmon, A Ostman-Smith, I Watkins, H
Citation: E. Blair et al., Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energycompromise in disease pathogenesis, HUM MOL GEN, 10(11), 2001, pp. 1215-1220

Authors: Bing, W Knott, A Redwood, C Esposito, G Purcell, I Watkins, H Marston, S
Citation: W. Bing et al., Effect of hypertrophic cardiomyopathy mutations in human cardiac muscle alpha-tropomyosin (Asp175Asn and Glu180Gly) on the regulatory properties of human cardiac troponin determined by in vitro motility assay, J MOL CEL C, 32(8), 2000, pp. 1489-1498

Authors: Redwood, C Lohmann, K Bing, W Esposito, GM Elliott, K Abdulrazzak, H Knott, A Purcell, I Marston, S Watkins, H
Citation: C. Redwood et al., Investigation of a truncated cardiac troponin T that causes familial hypertrophic cardiomyopathy - Ca2+ regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type protein, CIRCUL RES, 86(11), 2000, pp. 1146-1152
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