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Results:
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Results: 22
Authors:
Watkins, H
Citation: H. Watkins, Hypertrophic cardiomyopathy: from molecular and genetic mechanisms to clinical management, EUR H J SUP, 3(L), 2001, pp. L43-L50
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:
Keavney, B
Watkins, H
Citation: B. Keavney et H. Watkins, Evolution of genetic analysis strategies in coronary heart disease: a caseof unnatural selection?, EUR HEART J, 22(4), 2001, pp. 271-273
Authors:
Khogali, SS
Mayosi, BM
Beattie, JM
McKenna, WJ
Watkins, H
Poulton, J
Citation: Ss. Khogali et al., A common mitochondrial DNA variant associated with susceptibility to dilated cardiomyopathy in two different populations, LANCET, 357(9264), 2001, pp. 1265-1267
Authors:
Blair, E
Price, SJ
Baty, CJ
Ostman-Smith, I
Watkins, H
Citation: E. Blair et al., Mutations in cis can confound genotype-phenotype correlations in hypertrophic cardiomyopathy, J MED GENET, 38(6), 2001, pp. 385-387
Authors:
Price, SJ
Greaves, DR
Watkins, H
Citation: Sj. Price et al., Identification of novel, functional genetic variants in the human matrix metalloproteinase-2 gene - Role of Sp1 in allele-specific transcriptional regulation, J BIOL CHEM, 276(10), 2001, pp. 7549-7558
Authors:
Cardon, LR
Watkins, H
Citation: Lr. Cardon et H. Watkins, Waiting for the working draft from the human genome project - A huge achievement, but not of immediate medical use, BR MED J, 320(7244), 2000, pp. 1223-1224
Authors:
Watkins, H
Citation: H. Watkins, Sudden death in hypertrophic cardiomyopathy., N ENG J MED, 342(6), 2000, pp. 422-424
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:
Elliott, K
Watkins, H
Redwood, CS
Citation: K. Elliott et al., Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy, J BIOL CHEM, 275(29), 2000, pp. 22069-22074
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
Authors:
Mayosi, B
Blair, E
Watkins, H
Citation: B. Mayosi et al., Dilated cardiomyopathy and the desmin gene, CIRCULATION, 102(13), 2000, pp. E100-E100
Authors:
Farza, H
Watkins, H
Citation: H. Farza et H. Watkins, Animal models of familial hypertrophic cardiomyopathy, MOL MED TOD, 5(12), 1999, pp. 544-545
Authors:
Zhang, BP
Henney, A
Eriksson, P
Hamsten, A
Watkins, H
Ye, S
Citation: Bp. Zhang et al., Genetic variation at the matrix metalloproteinase-9 locus on chromosome 20q12.2-13.1, HUM GENET, 105(5), 1999, pp. 418-423
Authors:
Green, FR
Watkins, H
Citation: Fr. Green et H. Watkins, Genetic association studies in coronary disease: the case of GPIIb-IIIa polymorphisms, EUR HEART J, 20(10), 1999, pp. 706-708
Authors:
Manolis, EN
Eavey, RD
Sangwatanaroj, S
Halpin, C
Rosenbaum, S
Watkins, H
Jarcho, J
Seidman, CE
Seidman, JG
Citation: En. Manolis et al., Hereditary postlingual sensorineural hearing loss mapping to chromosome Xq21, AM J OTOL, 20(5), 1999, pp. 621-626
Authors:
Mayosi, BM
Watkins, H
Citation: Bm. Mayosi et H. Watkins, Impact of molecular genetics on clinical cardiology, J ROY COL P, 33(2), 1999, pp. 124-131
Authors:
Mayosi, BM
Khogali, SS
Zhang, BP
Watkins, H
Citation: Bm. Mayosi et al., Cardiac and skeletal actin gene mutations are not a common cause of dilated cardiomyopathy, J MED GENET, 36(10), 1999, pp. 796-797
Authors:
Ye, S
Whatling, C
Watkins, H
Henney, A
Citation: S. Ye et al., Human stromelysin gene promoter activity is modulated by transcription factor ZBP-89, FEBS LETTER, 450(3), 1999, pp. 268-272
Authors:
Zhang, BP
Ye, S
Herrmann, SM
Eriksson, P
de Maat, M
Evans, A
Arveiler, D
Luc, G
Cambien, F
Hamsten, A
Watkins, H
Henney, AM
Citation: Bp. Zhang et al., Functional polymorphism in the regulatory region of gelatinase B gene in relation to severity of coronary atherosclerosis, CIRCULATION, 99(14), 1999, pp. 1788-1794
Authors:
Redwood, CS
Moolman-Smook, JC
Watkins, H
Citation: Cs. Redwood et al., Properties of mutant contractile proteins that cause hypertrophic cardiomyopathy, CARDIO RES, 44(1), 1999, pp. 20-36
Authors:
Baty, C
Watkins, H
Citation: C. Baty et H. Watkins, Familial hypertrophic cardiomyopathy: man, mouse and cat, QJM-MON J A, 91(12), 1998, pp. 791-793
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