-
1
-
-
0029089583
-
Familial hypertrophic cardiomyopathy: A genetic model of cardiac hypertrophy
-
Watkins, H., J.G. Seidman, and C.E. Seidman. 1995. Familial hypertrophic cardiomyopathy: a genetic model of cardiac hypertrophy. Hum. Mol. Genet. 4:1721-1727.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1721-1727
-
-
Watkins, H.1
Seidman, J.G.2
Seidman, C.E.3
-
2
-
-
0025040392
-
A molecular basis for familial hypertrophic cardiomyopathy: A beta cardiac myosin heavy chain gene missense mutation
-
Geisterfer-Lowrance, A.A., S. Kass, G. Tanigawa, H.P. Vosberg, W. McKenna, C.E. Seidman, and J.G. Seidman. 1990. A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation. Cell. 62:999-1006.
-
(1990)
Cell
, vol.62
, pp. 999-1006
-
-
Geisterfer-Lowrance, A.A.1
Kass, S.2
Tanigawa, G.3
Vosberg, H.P.4
McKenna, W.5
Seidman, C.E.6
Seidman, J.G.7
-
3
-
-
15844400653
-
Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle
-
Poetter, K., H. Jiang, S. Hassanzadeh, S.R. Master, A. Chang, M.C. Dalakas, I. Rayment, S.R. Sellers, L. Fananapazir, and N.D. Epstein. 1996. Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle. Nat. Genet. 13:63-69.
-
(1996)
Nat. Genet.
, vol.13
, pp. 63-69
-
-
Poetter, K.1
Jiang, H.2
Hassanzadeh, S.3
Master, S.R.4
Chang, A.5
Dalakas, M.C.6
Rayment, I.7
Sellers, S.R.8
Fananapazir, L.9
Epstein, N.D.10
-
4
-
-
0028178083
-
Mutations in a tropomyosin and in cardiac troponin T cause hypertrophic cardiomyopathy: A disease of the sarcomere
-
Thierfelder, L., H. Watkins, C. MacRae, R. Lamas, H.P. Vosberg, W.J. McKenna, J.G. Seidman, and C.E. Seidman. 1994. Mutations in a tropomyosin and in cardiac troponin T cause 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
Lamas, R.4
Vosberg, H.P.5
McKenna, W.J.6
Seidman, J.G.7
Seidman, C.E.8
-
5
-
-
0028844204
-
Mutations in the cardiac myosin binding protein C gene on chromosome 11 cause familial hypertrophic cardiomyopathy
-
Watkins, H., D. Conner, L. Thierfelder, J. A. Jarcho, C. MacRae, W.J. McKenna, B.J. Maron, J.G. Seidman, and C.E. Seidman. 1995. Mutations in the cardiac myosin binding protein C gene on chromosome 11 cause familial hypertrophic cardiomyopathy. Nat. Genet. 11:434-437.
-
(1995)
Nat. Genet.
, vol.11
, pp. 434-437
-
-
Watkins, H.1
Conner, D.2
Thierfelder, L.3
Jarcho, J.A.4
MacRae, C.5
McKenna, W.J.6
Maron, B.J.7
Seidman, J.G.8
Seidman, C.E.9
-
6
-
-
0028886136
-
Cardiac myosin binding protein C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy
-
Bonne, G., L. Carrier, J. Bercovici, C. Cruaud, P. Richard, B. Hainque, M. Gautel, S. Labeit, M. James, J. Beckmann, J. Weissenbach, H.P. Vosberg, M. Fiszman, M. Komajda, and K. Schwartz. 1995. Cardiac myosin binding protein C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy. Nat. Genet. 11:438-440.
-
(1995)
Nat. Genet.
, vol.11
, pp. 438-440
-
-
Bonne, G.1
Carrier, L.2
Bercovici, J.3
Cruaud, C.4
Richard, P.5
Hainque, B.6
Gautel, M.7
Labeit, S.8
James, M.9
Beckmann, J.10
Weissenbach, J.11
Vosberg, H.P.12
Fiszman, M.13
Komajda, M.14
Schwartz, K.15
-
7
-
-
0026573969
-
Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy
-
Watkins, H., A. Rosenzweig, D.S. Hwang, T. Levi, W.J. McKenna, C.E. Seidman, and J.G. Seidman. 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.J.5
Seidman, C.E.6
Seidman, J.G.7
-
8
-
-
0028999347
-
A myosin missense mutation, not a null allele, causes familial hypertrophic cardiomyopathy
-
Nishi, H., A. Kimura, H. Harada, Y. Koga, K. Adachi, K. Matsuyama, T. Koyanagi, S. Yasunaga, T. Imaizumi, H. Toshima, and T. Sasazuki. 1995. A myosin missense mutation, not a null allele, causes familial hypertrophic cardiomyopathy. Circulation. 91:2911-2915.
-
(1995)
Circulation
, vol.91
, pp. 2911-2915
-
-
Nishi, H.1
Kimura, A.2
Harada, H.3
Koga, Y.4
Adachi, K.5
Matsuyama, K.6
Koyanagi, T.7
Yasunaga, S.8
Imaizumi, T.9
Toshima, H.10
Sasazuki, T.11
-
9
-
-
0025162268
-
Functions of the myosin ATP and actin binding sites are required for C. elegans thick filament assembly
-
Bejsovec, A., and P. Anderson. 1990. Functions of the myosin ATP and actin binding sites are required for C. elegans thick filament assembly. Cell. 60: 133-140.
-
(1990)
Cell
, vol.60
, pp. 133-140
-
-
Bejsovec, A.1
Anderson, P.2
-
10
-
-
0027980111
-
Heterologous expression of a cardiomyopathic myosin that is defective in its actin interaction
-
Sweeney, H.L., A.J. Straceski, L.A. Leinwand, B.A. Tikunov, and L. Faust. 1994. Heterologous expression of a cardiomyopathic myosin that is defective in its actin interaction. J. Biol. Chem. 269:1603-1605.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 1603-1605
-
-
Sweeney, H.L.1
Straceski, A.J.2
Leinwand, L.A.3
Tikunov, B.A.4
Faust, L.5
-
11
-
-
0027302431
-
Skeletal muscle expression and abnormal function of β-myosin in hypertrophic cardiomyopathy
-
Cuda, G., L. Fananapazir, W.S. Zhu, J.R. Sellers, and N.D. Epstein. 1993. Skeletal muscle expression and abnormal function of β-myosin in hypertrophic cardiomyopathy. J. Clin. Invest. 91:2861-2865.
-
(1993)
J. Clin. Invest.
, vol.91
, pp. 2861-2865
-
-
Cuda, G.1
Fananapazir, L.2
Zhu, W.S.3
Sellers, J.R.4
Epstein, N.D.5
-
12
-
-
0028967729
-
Abnormal contractile properties of muscle fibers expressing β-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy
-
Lankford, E.B., N.D. Epstein, L. Fananapazir, and H.L. Sweeney. 1995. Abnormal contractile properties of muscle fibers expressing β-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy. J. Clin. Invest. 95:1409-1414.
-
(1995)
J. Clin. Invest.
, vol.95
, pp. 1409-1414
-
-
Lankford, E.B.1
Epstein, N.D.2
Fananapazir, L.3
Sweeney, H.L.4
-
13
-
-
0028902929
-
Mutations in the genes for cardiac troponin T and a tropomyosin in hypertrophic cardiomyopathy
-
Watkins, H., W.J. McKenna, L. Thierfelder, H.S. Suk, R. Anan, P. Spirito, A. Matsumori, C. Moravec, J.G. Seidman, and C.E. Seidman. 1995. Mutations in the genes for cardiac troponin T and a tropomyosin in hypertrophic cardiomyopathy. N. Engl. J. Med. 332:1058-1064.
-
(1995)
N. Engl. J. Med.
, vol.332
, pp. 1058-1064
-
-
Watkins, H.1
McKenna, W.J.2
Thierfelder, L.3
Suk, H.S.4
Anan, R.5
Spirito, P.6
Matsumori, A.7
Moravec, C.8
Seidman, J.G.9
Seidman, C.E.10
-
14
-
-
0019480434
-
Electron microscopic and electrophoretic studies of a Drosophila muscle mutant wings-up B
-
Mogami, K., Y. Nonomura, and Y. Hotta. 1981. Electron microscopic and electrophoretic studies of a Drosophila muscle mutant wings-up B. Jpn. J. Genet. 56:51-65.
-
(1981)
Jpn. J. Genet.
, vol.56
, pp. 51-65
-
-
Mogami, K.1
Nonomura, Y.2
Hotta, Y.3
-
15
-
-
0029007607
-
Familial hypertrophic cardiomyopathy. Nonsense versus missense mutations
-
Schwartz, K. 1995. Familial hypertrophic cardiomyopathy. Nonsense versus missense mutations. Circulation. 91:2865-2867.
-
(1995)
Circulation
, vol.91
, pp. 2865-2867
-
-
Schwartz, K.1
-
16
-
-
0030004861
-
Thin filament-mediated regulation of cardiac contraction
-
Tobacman, L.S. 1996. Thin filament-mediated regulation of cardiac contraction. Ann. Rev. Physiol. 58:751-792.
-
(1996)
Ann. Rev. Physiol.
, vol.58
, pp. 751-792
-
-
Tobacman, L.S.1
-
17
-
-
0021324088
-
The current status of myocardial disarray in hypertrophic cardiomyopathy
-
Davies, M.J. 1984. The current status of myocardial disarray in hypertrophic cardiomyopathy. Br. Heart J. 51:361-363.
-
(1984)
Br. Heart J.
, vol.51
, pp. 361-363
-
-
Davies, M.J.1
-
18
-
-
0026349336
-
Regulation of cardiac gene expression during myocardial growth and hypertrophy: Molecular studies of an adaptive physiologic response
-
Chien, K.R., K.U. Knowlton, H. Zhu, and S. Chien. 1991. Regulation of cardiac gene expression during myocardial growth and hypertrophy: molecular studies of an adaptive physiologic response. FASEB J. 5:3037-3046.
-
(1991)
FASEB J.
, vol.5
, pp. 3037-3046
-
-
Chien, K.R.1
Knowlton, K.U.2
Zhu, H.3
Chien, S.4
-
19
-
-
0026028336
-
Growth factors, proto-oncogenes, and plasticity of the cardiac phenotype
-
Parker, T.G., and M.D. Schneider. 1991. Growth factors, proto-oncogenes, and plasticity of the cardiac phenotype. Annu. Rev. Physiol 53:179-200.
-
(1991)
Annu. Rev. Physiol
, vol.53
, pp. 179-200
-
-
Parker, T.G.1
Schneider, M.D.2
-
20
-
-
0027722248
-
Autocrine release of angiotensin II mediates stretch induced hypertrophy of cardiac myocytes in vitro
-
Sadoshima, J., Y. Xu, H. S. Slayter, and S. Izumo. 1993. Autocrine release of angiotensin II mediates stretch induced hypertrophy of cardiac myocytes in vitro. Cell. 75:977-984.
-
(1993)
Cell
, vol.75
, pp. 977-984
-
-
Sadoshima, J.1
Xu, Y.2
Slayter, H.S.3
Izumo, S.4
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