Knowlton, K U; Rockman, H A; Itani, M et al. (1995) Divergent pathways mediate the induction of ANF transgenes in neonatal and hypertrophic ventricular myocardium. J Clin Invest 96:1311-8
|
Anan, R; Greve, G; Thierfelder, L et al. (1994) Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy. J Clin Invest 93:280-5
|
MacRae, C A; Watkins, H C; Jarcho, J A et al. (1994) An evaluation of ribonuclease protection assays for the detection of beta-cardiac myosin heavy chain gene mutations. Circulation 89:33-5
|
Thierfelder, L; Watkins, H; MacRae, C et al. (1994) Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere. Cell 77:701-12
|
Solomon, S D; Wolff, S; Watkins, H et al. (1993) Left ventricular hypertrophy and morphology in familial hypertrophic cardiomyopathy associated with mutations of the beta-myosin heavy chain gene. J Am Coll Cardiol 22:498-505
|
Watkins, H; MacRae, C; Thierfelder, L et al. (1993) A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3. Nat Genet 3:333-7
|
Watkins, H; Thierfelder, L; Anan, R et al. (1993) Independent origin of identical beta cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathy. Am J Hum Genet 53:1180-5
|
Watkins, H; Thierfelder, L; Hwang, D S et al. (1992) Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations. J Clin Invest 90:1666-71
|
Watkins, H; Seidman, C E; MacRae, C et al. (1992) Progress in familial hypertrophic cardiomyopathy: molecular genetic analyses in the original family studied by Teare. Br Heart J 67:34-8
|
Seidman, C E; Seidman, J G (1991) Mutations in cardiac myosin heavy chain genes cause familial hypertrophic cardiomyopathy. Mol Biol Med 8:159-66
|
Showing the most recent 10 out of 14 publications