-
1
-
-
0030009858
-
Triggers for sudden cardiac death in the athlete
-
Maron, B.J. 1996. Triggers for sudden cardiac death in the athlete. Card. Clinics. 14:195-210.
-
(1996)
Card. Clinics
, vol.14
, pp. 195-210
-
-
Maron, B.J.1
-
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
-
-
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, et al. 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
-
4
-
-
0030765610
-
Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy
-
Kimura, A., H. Harada, J.-E. Park, H. Nishi, M. Satob, M. Takahashi, S. Hiroi, T. Sasaoka, N. Ohbuchi, T. Nakamura, et al. 1997. Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy. Nat. Genet. 16:379-382.
-
(1997)
Nat. Genet.
, vol.16
, pp. 379-382
-
-
Kimura, A.1
Harada, H.2
Park, J.-E.3
Nishi, H.4
Satob, M.5
Takahashi, M.6
Hiroi, S.7
Sasaoka, T.8
Ohbuchi, N.9
Nakamura, T.10
-
5
-
-
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, J.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, J.R.8
Fananapazir, L.9
Epstein, N.D.10
-
6
-
-
0028178083
-
Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere
-
Thierfelder, L., H. Watkins, C. MacRae, R. Lamas, W. McKenna, H.P. Vosberg, J.G. Seidman, and C.E. Seidman. 1994. Alpha-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
Lamas, R.4
McKenna, W.5
Vosberg, H.P.6
Seidman, J.G.7
Seidman, C.E.8
-
7
-
-
0028902929
-
Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy
-
Watkins, H., W.J. McKenna, L. Thierfelder, H.J. Suk, R. Anan, A. O'Donoghue, P. Spirito, A. Matsumori, C.S. Moravec, J.G. Seidman, and C.E. Seidman. 1995. Mutations in the genes for cardiac troponin T and alpha-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.J.4
Anan, R.5
O'Donoghue, A.6
Spirito, P.7
Matsumori, A.8
Moravec, C.S.9
Seidman, J.G.10
Seidman, C.E.11
-
8
-
-
0029143611
-
Familial hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3
-
MacRae, C.A., N. Ghaisas, S. Kass, S. Donnelly, C.T. Basson, H.C. Watkins, R. Anan, L.H. Thierfelder, K. McGarry, and E.E.A. Rowland. 1995. Familial hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3. J. Clin. Invest. 96:1216-1220.
-
(1995)
J. Clin. Invest.
, vol.96
, pp. 1216-1220
-
-
MacRae, C.A.1
Ghaisas, N.2
Kass, S.3
Donnelly, S.4
Basson, C.T.5
Watkins, H.C.6
Anan, R.7
Thierfelder, L.H.8
McGarry, K.9
Rowland, E.E.A.10
-
9
-
-
0030091595
-
Titin as a scaffold and spring. Cytoskeleton
-
Trinick, J. 1996. Titin as a scaffold and spring. Cytoskeleton. Curr. Biol. 6:258-260.
-
(1996)
Curr. Biol.
, vol.6
, pp. 258-260
-
-
Trinick, J.1
-
10
-
-
0015924821
-
A new protein of the thick filaments of vertebrate skeletal myofibrils. Extraction, purification and characterization
-
Offer, G., C. Moos, and R. Starr. 1973. A new protein of the thick filaments of vertebrate skeletal myofibrils. Extraction, purification and characterization. J. Mol. Biol. 74:653-676.
-
(1973)
J. Mol. Biol.
, vol.74
, pp. 653-676
-
-
Offer, G.1
Moos, C.2
Starr, R.3
-
11
-
-
0030052266
-
A molecular map of the interactions between titin and myosin-binding protein C. Implications for sarcomeric assembly in familial hypertrophic cardiomyopathy
-
Freiburg, A., and M. Gautel. 1996. A molecular map of the interactions between titin and myosin-binding protein C. Implications for sarcomeric assembly in familial hypertrophic cardiomyopathy. Eur. J. Biochem. 235:317-323.
-
(1996)
Eur. J. Biochem.
, vol.235
, pp. 317-323
-
-
Freiburg, A.1
Gautel, M.2
-
12
-
-
0030027029
-
Modulation of myosin filament organization by c-protein family members
-
Seiler, S.H., D.A. Fischman, and L.A. Leinwand. 1996. Modulation of myosin filament organization by c-protein family members. Mol Biol. Cell. 7: 113-127.
-
(1996)
Mol Biol. Cell
, vol.7
, pp. 113-127
-
-
Seiler, S.H.1
Fischman, D.A.2
Leinwand, L.A.3
-
13
-
-
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
-
14
-
-
17344372574
-
Molecular pathology of familial hypertrophic cardiomyopathy caused by mutations in the cardiac myosin binding protein C gene
-
Yu, B., J.A. French, L. Carrier, R.W. Jeremy, D.R. McTaggart, M.R. Nicholson, B. Hambly, C. Semsarian, D.R. Richmond, K. Schwartz, and R.J. Trent. 1998. Molecular pathology of familial hypertrophic cardiomyopathy caused by mutations in the cardiac myosin binding protein C gene. J. Med. Genet. 35:205-210.
-
(1998)
J. Med. Genet.
, vol.35
, pp. 205-210
-
-
Yu, B.1
French, J.A.2
Carrier, L.3
Jeremy, R.W.4
McTaggart, D.R.5
Nicholson, M.R.6
Hambly, B.7
Semsarian, C.8
Richmond, D.R.9
Schwartz, K.10
Trent, R.J.11
-
15
-
-
0032011430
-
Identification of a new missense mutation in MyBP-C associated with hypertrophic cardiomyopathy
-
Moolman-Smook, J.C., B. Mayosi, P. Brink, and V.A. Corfieid. 1998. Identification of a new missense mutation in MyBP-C associated with hypertrophic cardiomyopathy. J. Med. Genet. 35:253-254.
-
(1998)
J. Med. Genet.
, vol.35
, pp. 253-254
-
-
Moolman-Smook, J.C.1
Mayosi, B.2
Brink, P.3
Corfieid, V.A.4
-
16
-
-
0031055854
-
Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy
-
Carrier, L., G. Bonne, E. Bahrend, B. Yu, P. Richard, F. Niel, B. Hainque, C. Cruaud, F. Gary, S. Labeit, et al. 1997. Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy. Circ. Res. 80:427-434.
-
(1997)
Circ. Res.
, vol.80
, pp. 427-434
-
-
Carrier, L.1
Bonne, G.2
Bahrend, E.3
Yu, B.4
Richard, P.5
Niel, F.6
Hainque, B.7
Cruaud, C.8
Gary, F.9
Labeit, S.10
-
17
-
-
0030030825
-
The carboxyl terminus of myosin binding protein C (MyBP-C, C-protein) specifies incorporation into the A-band of striated muscle
-
Gilbert, R., M.G. Kelly, T. Mikawa, and D.A. Fischman. 1996. The carboxyl terminus of myosin binding protein C (MyBP-C, C-protein) specifies incorporation into the A-band of striated muscle. J. Cell Sci. 109:101-111.
-
(1996)
J. Cell Sci.
, vol.109
, pp. 101-111
-
-
Gilbert, R.1
Kelly, M.G.2
Mikawa, T.3
Fischman, D.A.4
-
18
-
-
0027515217
-
The major myosin-binding domain of skeletal muscle MyBP-C (C protein) resides in the COOH-terminal, immunoglobulin C2 motif
-
Okagaki, T., F.E. Weber, D.A. Fischman, K.T. Vaughan, T. Mikawa, and F.C. Reinach. 1993. The major myosin-binding domain of skeletal muscle MyBP-C (C protein) resides in the COOH-terminal, immunoglobulin C2 motif. J. Cell Biol. 123:619-626.
-
(1993)
J. Cell Biol.
, vol.123
, pp. 619-626
-
-
Okagaki, T.1
Weber, F.E.2
Fischman, D.A.3
Vaughan, K.T.4
Mikawa, T.5
Reinach, F.C.6
-
19
-
-
0027494274
-
Determinants of loaded shortening velocity in single cardiac myocytes permeabilized with alpha-hemolysin
-
Sweitzer, N.K., and R.L. Moss. 1993. Determinants of loaded shortening velocity in single cardiac myocytes permeabilized with alpha-hemolysin. Circ. Res. 73:1150-1162.
-
(1993)
Circ. Res.
, vol.73
, pp. 1150-1162
-
-
Sweitzer, N.K.1
Moss, R.L.2
-
20
-
-
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
-
21
-
-
0030852878
-
Novel splice donor site mutation in the cardiac myosin-binding protein-C gene in familial hypertrophic cardiomyopathy
-
Rottbauer, W., M. Gautel, J. Zehelein, S. Labeit, W.M. Franz, C. Fischer, B. Vollrath, G. Mall, R. Dietz, W. Kubier, and H.A. Katus. 1997. Novel splice donor site mutation in the cardiac myosin-binding protein-C gene in familial hypertrophic cardiomyopathy.J. Clin. Invest. 100:475-482.
-
(1997)
J. Clin. Invest.
, vol.100
, pp. 475-482
-
-
Rottbauer, W.1
Gautel, M.2
Zehelein, J.3
Labeit, S.4
Franz, W.M.5
Fischer, C.6
Vollrath, B.7
Mall, G.8
Dietz, R.9
Kubier, W.10
Katus, H.A.11
-
22
-
-
0028094767
-
Autoimmune myocarditis induced in mice by cardiac C-protcin. Cloning of complementary DNA encoding murine cardiac C-protein and partial characterization of the antigenic peptides
-
Kasahara, H., M. Itoh, T. Sugiyama, N. Kido, H. Hayashi, H. Saito, S. Tsukita, and N. Kato. 1994. Autoimmune myocarditis induced in mice by cardiac C-protcin. Cloning of complementary DNA encoding murine cardiac C-protein and partial characterization of the antigenic peptides.J. Clin. Invest. 94:1026-1036.
-
(1994)
J. Clin. Invest.
, vol.94
, pp. 1026-1036
-
-
Kasahara, H.1
Itoh, M.2
Sugiyama, T.3
Kido, N.4
Hayashi, H.5
Saito, H.6
Tsukita, S.7
Kato, N.8
-
23
-
-
0030023987
-
Transgenic remodeling of the contractile apparatus in the mammalian heart
-
Palermo, J., J. Gulick, M. Colbert, J. Fewell, and J. Robbins. 1996. Transgenic remodeling of the contractile apparatus in the mammalian heart. Circ. Res. 78:504-509.
-
(1996)
Circ. Res.
, vol.78
, pp. 504-509
-
-
Palermo, J.1
Gulick, J.2
Colbert, M.3
Fewell, J.4
Robbins, J.5
-
24
-
-
0025817320
-
Troponin T expression in normal and pressure-loaded fetal sheep heart
-
McAuliffe, J.J., and J. Robbins. 1991. Troponin T expression in normal and pressure-loaded fetal sheep heart. Pediatr. Res. 29:580-585.
-
(1991)
Pediatr. Res.
, vol.29
, pp. 580-585
-
-
McAuliffe, J.J.1
Robbins, J.2
-
25
-
-
0032526249
-
Functional significance of cardiac myosin essential light chain isoform switching in transgenic mice
-
Fewell, J., T.E. Hewett, R. Klevitsky, E. Hayes, D. Warshaw, A. Sanbe, D. Maughan, and J. Robbins. 1998. Functional significance of cardiac myosin essential light chain isoform switching in transgenic mice. J. Clin. Invest. 101:2639-2651.
-
(1998)
J. Clin. Invest.
, vol.101
, pp. 2639-2651
-
-
Fewell, J.1
Hewett, T.E.2
Klevitsky, R.3
Hayes, E.4
Warshaw, D.5
Sanbe, A.6
Maughan, D.7
Robbins, J.8
-
26
-
-
0018333803
-
The velocity of unloaded shortening and its relation to sarcomere length and isometric force in vertebrate muscle fibers
-
Edman, K.A.P. 1979. The velocity of unloaded shortening and its relation to sarcomere length and isometric force in vertebrate muscle fibers. J. Physiol. 291:143-159.
-
(1979)
J. Physiol.
, vol.291
, pp. 143-159
-
-
Edman, K.A.P.1
-
27
-
-
0022500567
-
Effects on shortening velocity of rabbit skeletal muscle due to variations in the level of thin-filament activation
-
Moss, R. 1986. Effects on shortening velocity of rabbit skeletal muscle due to variations in the level of thin-filament activation. J. Physiol. 377:487-505.
-
(1986)
J. Physiol.
, vol.377
, pp. 487-505
-
-
Moss, R.1
-
29
-
-
0030892526
-
Transgenic remodeling of the regulatory myosin light chains in the mammalian heart
-
Gulick, J., T.E. Hewett, R. Klevitsky, S. Buck, R.L. Moss, and J. Robbins. 1997. Transgenic remodeling of the regulatory myosin light chains in the mammalian heart. Circ. Res. 80:655-664.
-
(1997)
Circ. Res.
, vol.80
, pp. 655-664
-
-
Gulick, J.1
Hewett, T.E.2
Klevitsky, R.3
Buck, S.4
Moss, R.L.5
Robbins, J.6
-
30
-
-
0031891357
-
Genotype-phenotype correlations in familial hypertrophic cardiomyopathy. A comparison between mutations in the cardiac protein-C and the beta-myosin heavy chain genes
-
Charron, P., O. Dubourg, M. Desnos, R. Isnard, A. Hagege, G. Bonne, L. Carrier, F. Tesson, J.B. Bouhour, J.C. Buzzi, et al. 1998. Genotype-phenotype correlations in familial hypertrophic cardiomyopathy. A comparison between mutations in the cardiac protein-C and the beta-myosin heavy chain genes. Eur. Heart J. 19:139-145.
-
(1998)
Eur. Heart J.
, vol.19
, pp. 139-145
-
-
Charron, P.1
Dubourg, O.2
Desnos, M.3
Isnard, R.4
Hagege, A.5
Bonne, G.6
Carrier, L.7
Tesson, F.8
Bouhour, J.B.9
Buzzi, J.C.10
-
31
-
-
0002500194
-
Gene defects that cause inherited cardiomyopathy
-
W.B. Saunders Co., Philadelphia, PA
-
Seidman, C.E., and J.G. Seidman. 1998. Gene defects that cause inherited cardiomyopathy. In The Molecular Basis of Heart Disease. W.B. Saunders Co., Philadelphia, PA.
-
(1998)
The Molecular Basis of Heart Disease
-
-
Seidman, C.E.1
Seidman, J.G.2
-
32
-
-
0028171636
-
Multiple disease genes cause hypertrophic cardiomyopathy
-
Watkins, H. 1994. Multiple disease genes cause hypertrophic cardiomyopathy. Br. Heart J. 7296(Suppl.):S4-S9.
-
(1994)
Br. Heart J.
, vol.7296
, Issue.SUPPL.
-
-
Watkins, H.1
-
33
-
-
0030067394
-
A mouse model of familial hypertrophic cardiomyopathy
-
Geisterfer-Lowrance, A.A., M. Christe, D.A. Conner, J.S. Ingwall, F.J. Schoen, C.E. Seidman, and J.G. Seidman. 1996. A mouse model of familial hypertrophic cardiomyopathy. Science. 272:731-734.
-
(1996)
Science
, vol.272
, pp. 731-734
-
-
Geisterfer-Lowrance, A.A.1
Christe, M.2
Conner, D.A.3
Ingwall, J.S.4
Schoen, F.J.5
Seidman, C.E.6
Seidman, J.G.7
-
34
-
-
0029807438
-
Mice expressing mutant myosin heavy chains are a model for familial hypertrophic cardiomyopathy
-
Vikstrom, K.L., S.M. Factor, and L.A. Leinwand. 1996. Mice expressing mutant myosin heavy chains are a model for familial hypertrophic cardiomyopathy. Mol. Med. 2:556-567.
-
(1996)
Mol. Med.
, vol.2
, pp. 556-567
-
-
Vikstrom, K.L.1
Factor, S.M.2
Leinwand, L.A.3
-
35
-
-
0025727160
-
Cardiac myosin heavy chain mRNA expression and myocardial function in the mouse heart
-
Ng, W.A., I.L. Grupp, A. Subramaniam, and J. Robbins. 1991. Cardiac myosin heavy chain mRNA expression and myocardial function in the mouse heart. Circ. Res. 68:1742-1750.
-
(1991)
Circ. Res.
, vol.68
, pp. 1742-1750
-
-
Ng, W.A.1
Grupp, I.L.2
Subramaniam, A.3
Robbins, J.4
-
36
-
-
0030870284
-
A treadmill exercise regimen for identifying subtle cardiovascular phenotypes in transgenic mice
-
Fewell, J.G., H. Osinska, R. Klevitsky, W.E. Ng, G. Sfyris, F. Bahrehmand, and J. Robbins. 1997. A treadmill exercise regimen for identifying subtle cardiovascular phenotypes in transgenic mice. Am. J. Physiol. 273:H1595-H1605.
-
(1997)
Am. J. Physiol.
, vol.273
-
-
Fewell, J.G.1
Osinska, H.2
Klevitsky, R.3
Ng, W.E.4
Sfyris, G.5
Bahrehmand, F.6
Robbins, J.7
-
37
-
-
10244221064
-
Ablation of the murine alpha myosin heavy chain gene leads to dosage effects and functional deficits in the heart
-
Jones, W.K., I.L. Grupp, T. Doetschman, G. Grupp, H. Osinska, T.E. Hewett, G. Boivin, J. Gulick, W.A. Ng, and J. Robbins. 1996. Ablation of the murine alpha myosin heavy chain gene leads to dosage effects and functional deficits in the heart. J. Clin. Invest. 98:1906-1917.
-
(1996)
J. Clin. Invest.
, vol.98
, pp. 1906-1917
-
-
Jones, W.K.1
Grupp, I.L.2
Doetschman, T.3
Grupp, G.4
Osinska, H.5
Hewett, T.E.6
Boivin, G.7
Gulick, J.8
Ng, W.A.9
Robbins, J.10
-
38
-
-
0032580520
-
Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy
-
Niimura, H., L.L. Bachinski, S. Sangwatanaroj, H. Watkins, A.E. Chudley, W. McKenma, A. Kristinsson, R. Roberts, M. Sole, B.J. Maron, et al. 1998. Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy. N. Engl. J. Med. 338:1248-1257.
-
(1998)
N. Engl. J. Med.
, vol.338
, pp. 1248-1257
-
-
Niimura, H.1
Bachinski, L.L.2
Sangwatanaroj, S.3
Watkins, H.4
Chudley, A.E.5
McKenma, W.6
Kristinsson, A.7
Roberts, R.8
Sole, M.9
Maron, B.J.10
|