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Volumn 93, Issue 3, 1998, Pages 13-16

Molecular genetic studies of familial hypertrophic cardiomyopathy

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL MODEL; ENVIRONMENTAL FACTOR; FAMILIAL DISEASE; GENE MUTATION; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; MOLECULAR GENETICS; MOUSE; NONHUMAN; SHORT SURVEY;

EID: 0032428460     PISSN: 01759418     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Short Survey
Times cited : (79)

References (20)
  • 1
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    • Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophie cardiomyopathy
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    • Bonne, G.1    Carrier, L.2    Bercovici, J.3
  • 3
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    • Idiopathic hypertrophic subaortic stenosis: Clinical analysis of 126 patients with emphasis on the natural history
    • Frank S, Braunwald E (1968) Idiopathic hypertrophic subaortic stenosis: Clinical analysis of 126 patients with emphasis on the natural history. Circulation 37: 759-88
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    • Frank, S.1    Braunwald, E.2
  • 4
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    • Phosphorylation switches specific for the cardiac isoform of myosin binding protein-C: A modulator of cardiac contraction?
    • Gautel M, Zuffardi O, Freiburg A, Labeit S (1995) Phosphorylation switches specific for the cardiac isoform of myosin binding protein-C: A modulator of cardiac contraction? EMBO 14: 1952-1960
    • (1995) EMBO , vol.14 , pp. 1952-1960
    • Gautel, M.1    Zuffardi, O.2    Freiburg, A.3    Labeit, S.4
  • 7
    • 0023130164 scopus 로고
    • Hypertrophic cardiomyopathy: Interrelations of clinical manifestations, pathophysiology, and therapy
    • Maron BJ, Bonow RO, Cannon RO III, Leon MB, Epstein SE (1987) Hypertrophic cardiomyopathy: Interrelations of clinical manifestations, pathophysiology, and therapy. N Engl J Med 316: 780-9 and 844-52
    • (1987) N Engl J Med , vol.316 , pp. 780-789
    • Maron, B.J.1    Bonow, R.O.2    Cannon III, R.O.3    Leon, M.B.4    Epstein, S.E.5
  • 8
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    • Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA study
    • Maron BJ, Gardin JM, Flack JM, Gidding SS, Kurosaki TT, Bild DE (1995) Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA study. Circulation 92: 785-9
    • (1995) Circulation , vol.92 , pp. 785-789
    • Maron, B.J.1    Gardin, J.M.2    Flack, J.M.3    Gidding, S.S.4    Kurosaki, T.T.5    Bild, D.E.6
  • 9
    • 0019458147 scopus 로고
    • Prognosis in hypertrophic cardiomyopathy: Role of age and clinical, electrocardiographic, and hemodynamic features
    • McKenna WJ, Deanfield J, Faruqui A, England D, Oakley CM, Goodwin JF (1981) Prognosis in hypertrophic cardiomyopathy: Role of age and clinical, electrocardiographic, and hemodynamic features. Am J Cardiol 47: 532-8
    • (1981) Am J Cardiol , vol.47 , pp. 532-538
    • McKenna, W.J.1    Deanfield, J.2    Faruqui, A.3    England, D.4    Oakley, C.M.5    Goodwin, J.F.6
  • 10
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    • Effect of C-protein on actomyosin ATPase
    • Moos C, Feng IM (1980) Effect of C-protein on actomyosin ATPase. Biochim Biophys Acta 632: 141-149
    • (1980) Biochim Biophys Acta , vol.632 , pp. 141-149
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  • 12
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    • Phosphorylation of chick cardiac C-protein by calcium/calmodulin-dependent protein kinase II
    • Schlender K, Bean LJ (1991) Phosphorylation of chick cardiac C-protein by calcium/calmodulin-dependent protein kinase II. J Biol Chem 266: 2811-2817
    • (1991) J Biol Chem , vol.266 , pp. 2811-2817
    • Schlender, K.1    Bean, L.J.2
  • 14
    • 0027209383 scopus 로고
    • Left ventricular hypertrophy and morphology in familial hypertrophic cardiomyopathy associated with mutations of the beta-myosin heavy chain gene
    • Solomon SD, 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
    • (1993) J Am Coll Cardiol , vol.22 , pp. 498-505
    • Solomon, S.D.1    Wolff, S.2    Watkins, H.3
  • 16
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    • α-Tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere
    • Thierfelder L, Watkins H, MacRae C, Lumas R, McKenna W, Vosberg H-P, Seidman JG, Seidman CE (1994) α-Tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere. Cell 77: 701-712
    • (1994) Cell , vol.77 , pp. 701-712
    • Thierfelder, L.1    Watkins, H.2    MacRae, C.3    Lumas, R.4    McKenna, W.5    Vosberg, H.-P.6    Seidman, J.G.7    Seidman, C.E.8
  • 19
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    • Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy
    • Watkins H, Rosenzweig A, Hwang DS, Levi T, McKenna W, Seidman CE, Seidman JG (1992) Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy. N Engl J Med 326: 1108-1114
    • (1992) N Engl J Med , vol.326 , pp. 1108-1114
    • Watkins, H.1    Rosenzweig, A.2    Hwang, D.S.3    Levi, T.4    McKenna, W.5    Seidman, C.E.6    Seidman, J.G.7
  • 20
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    • Expression and functional assessment of a truncated cardiac troponin T that causes hypertrophic cardiomyopathy: Evidence for a dominant negative action
    • in press
    • Watkins H, Seidman CE, Seidman JG, Feng HS, Sweeney HL (1997) Expression and functional assessment of a truncated cardiac troponin T that causes hypertrophic cardiomyopathy: evidence for a dominant negative action. J Clin Invest (in press)
    • (1997) J Clin Invest
    • Watkins, H.1    Seidman, C.E.2    Seidman, J.G.3    Feng, H.S.4    Sweeney, H.L.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.