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