-
1
-
-
0029166817
-
Recent advances in the molecular genetics of hypertrophic cardiomyopathy
-
Marian AJ, Roberts R: Recent advances in the molecular genetics of hypertrophic cardiomyopathy. Circulation 1995;92:1336-1347.
-
(1995)
Circulation
, vol.92
, pp. 1336-1347
-
-
Marian, A.J.1
Roberts, R.2
-
2
-
-
0028855776
-
Molecular basis of familial cardiomyopathies
-
Schwartz K, Carrier L, Guicheney P, et al: Molecular basis of familial cardiomyopathies. Circulation 1995; 91:532-540.
-
(1995)
Circulation
, vol.91
, pp. 532-540
-
-
Schwartz, K.1
Carrier, L.2
Guicheney, P.3
-
3
-
-
0029089583
-
Familial hypertrophic cardiomyopathy: A genetic model of cardiac hypertrophy
-
Watkins H, Seidman JG, Seidman CE. Familial hypertrophic cardiomyopathy: A genetic model of cardiac hypertrophy. Human Mol Genet 1995;4:1721-1727.
-
(1995)
Human Mol Genet
, vol.4
, pp. 1721-1727
-
-
Watkins, H.1
Seidman, J.G.2
Seidman, C.E.3
-
4
-
-
0015323807
-
Myocardial ultrastructure in idiopathic hypertrophic subaortic stenosis: A study of operatively excised left ventricular outflow tract muscle in 14 patients
-
Ferrans VJ, Morrow AG, Roberts WC: Myocardial ultrastructure in idiopathic hypertrophic subaortic stenosis: A study of operatively excised left ventricular outflow tract muscle in 14 patients. Circulation 1972;45:769-792.
-
(1972)
Circulation
, vol.45
, pp. 769-792
-
-
Ferrans, V.J.1
Morrow, A.G.2
Roberts, W.C.3
-
5
-
-
0030057106
-
Sudden death in young competitive athletes. Clinical, demographic, and pathological profiles
-
Maron BJ, Shirani J, Poliac LC, et al: Sudden death in young competitive athletes. Clinical, demographic, and pathological profiles. JAMA 1996;276;199-204.
-
(1996)
JAMA
, vol.276
, pp. 199-204
-
-
Maron, B.J.1
Shirani, J.2
Poliac, L.C.3
-
6
-
-
0029083650
-
Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIa Study
-
Coronary Artery Risk Development in Adults
-
Maron BJ, Gardin JM, Flack JM, et al: Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in Adults. Circulation 1995;92:785-789.
-
(1995)
Circulation
, vol.92
, pp. 785-789
-
-
Maron, B.J.1
Gardin, J.M.2
Flack, J.M.3
-
7
-
-
0020622972
-
Hypertrophic cardiomyopathy and its markers in the general population. The great masquerader revisited: The Framingham Study
-
Savage DD, Castelli WP, Abbott RO, et al: Hypertrophic cardiomyopathy and its markers in the general population. The great masquerader revisited: The Framingham Study. J Cardiovasc Ultrasonogr 1983:2:41-47.
-
(1983)
J Cardiovasc Ultrasonogr
, vol.2
, pp. 41-47
-
-
Savage, D.D.1
Castelli, W.P.2
Abbott, R.O.3
-
8
-
-
0024522202
-
Clinical course and prognosis of hypertrophic cardiomyopathy in an outpatient population
-
Spirito P, Chiarella F, Carratino L, et al: Clinical course and prognosis of hypertrophic cardiomyopathy in an outpatient population. N Engl J Med 1989;320:749-755.
-
(1989)
N Engl J Med
, vol.320
, pp. 749-755
-
-
Spirito, P.1
Chiarella, F.2
Carratino, L.3
-
9
-
-
0027491649
-
Prognosis in hypertrophic cardiomyopathy observed in a large clinic population
-
Kofflard MJ, Waldstein DJ, Vos J, et al: Prognosis in hypertrophic cardiomyopathy observed in a large clinic population. Am J Cardiol 1993;72:939-943.
-
(1993)
Am J Cardiol
, vol.72
, pp. 939-943
-
-
Kofflard, M.J.1
Waldstein, D.J.2
Vos, J.3
-
10
-
-
0027521108
-
Impact of patient selection biases on the perception of hypertrophic cardiomyopathy and its natural history
-
Maron BJ, Spirito P: Impact of patient selection biases on the perception of hypertrophic cardiomyopathy and its natural history. Am J Cardiol 1993;72:970-972.
-
(1993)
Am J Cardiol
, vol.72
, pp. 970-972
-
-
Maron, B.J.1
Spirito, P.2
-
11
-
-
0019458147
-
Prognosis in hypertrophic cardiomyopathy: Role of age and clinical electrocardiographic and hemodynamic features
-
McKenna W, Deanfield J, Farugui A, et al: Prognosis in hypertrophic cardiomyopathy: Role of age and clinical electrocardiographic and hemodynamic features. Am J Cardiol 1981;47:532-538.
-
(1981)
Am J Cardiol
, vol.47
, pp. 532-538
-
-
McKenna, W.1
Deanfield, J.2
Farugui, A.3
-
12
-
-
0028178083
-
α-Tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere
-
Thierfelder L, Watkins H, MacRae C, et al: α-Tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere. Cell 1994;77:701-712.
-
(1994)
Cell
, vol.77
, pp. 701-712
-
-
Thierfelder, L.1
Watkins, H.2
MacRae, C.3
-
13
-
-
0025040392
-
A molecular basis for familial hypertrophic cardiomyopathy: A β-cardiac myosin heavy chain gene missense mutation
-
Geisterfer-Lawrance AA, Kass S, Tanigawa G, et al: A molecular basis for familial hypertrophic cardiomyopathy: A β-cardiac myosin heavy chain gene missense mutation. Cell 1990;62:999-1006.
-
(1990)
Cell
, vol.62
, pp. 999-1006
-
-
Geisterfer-Lawrance, A.A.1
Kass, S.2
Tanigawa, G.3
-
14
-
-
0028844204
-
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy
-
Watkins H, Conner D, Thierfelder L, et al: Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy. Nature Genetics 1995;11:434-437
-
(1995)
Nature Genetics
, vol.11
, pp. 434-437
-
-
Watkins, H.1
Conner, D.2
Thierfelder, L.3
-
15
-
-
0028886136
-
Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy
-
Bonne G, Carrier L, Bercovici J, et al: Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy. Nature Genetics 1995;11:438-440.
-
(1995)
Nature Genetics
, vol.11
, pp. 438-440
-
-
Bonne, G.1
Carrier, L.2
Bercovici, J.3
-
16
-
-
15844400653
-
Mutations in either the essential or regulatory light chains of myosin are associated with a rate myopathy in human heart and skeletal muscle
-
Poetter K, Jiang H, Hassanzadeh S, et al: Mutations in either the essential or regulatory light chains of myosin are associated with a rate myopathy in human heart and skeletal muscle. Nature Genet 1996;13:63-69.
-
(1996)
Nature Genet
, vol.13
, pp. 63-69
-
-
Poetter, K.1
Jiang, H.2
Hassanzadeh, S.3
-
17
-
-
0030765610
-
Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy
-
Kimura A, Harada H, Park J-E, et al: Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy. Nature Genet 1997;16:379-382.
-
(1997)
Nature Genet
, vol.16
, pp. 379-382
-
-
Kimura, A.1
Harada, H.2
Park, J.-E.3
-
18
-
-
0024426784
-
Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1
-
Jarcho JA, McKenna W, Pare JAP, et al: Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1. N Engl J Med 1989;321:1372-1378.
-
(1989)
N Engl J Med
, vol.321
, pp. 1372-1378
-
-
Jarcho, J.A.1
McKenna, W.2
Pare, J.A.P.3
-
19
-
-
0025727099
-
Localization of gene for familial hypertrophic cardiomyopathy to chromosome 14q1 in a diverse US population
-
Hejtmancik JF, Brink PA, Towbin J, et al: Localization of gene for familial hypertrophic cardiomyopathy to chromosome 14q1 in a diverse US population. Circulation 1991;83:1592-1597.
-
(1991)
Circulation
, vol.83
, pp. 1592-1597
-
-
Hejtmancik, J.F.1
Brink, P.A.2
Towbin, J.3
-
20
-
-
0026584365
-
Evidence of genetic heterogeneity in five kindreds with familial hypertrophic cardiomyopathy
-
Epstein ND, Fananapazir L, Lin HJ, et al: Evidence of genetic heterogeneity in five kindreds with familial hypertrophic cardiomyopathy. Circulation 1992;85:635-647.
-
(1992)
Circulation
, vol.85
, pp. 635-647
-
-
Epstein, N.D.1
Fananapazir, L.2
Lin, H.J.3
-
21
-
-
0027420155
-
A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3
-
Watkins H, MacRae C, Thierfelder L, et al: A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3. Nature (Genetics) 1993;3:333-337.
-
(1993)
Nature (Genetics)
, vol.3
, pp. 333-337
-
-
Watkins, H.1
MacRae, C.2
Thierfelder, L.3
-
22
-
-
0027180678
-
A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 15q2
-
Thierfelder LC, MacRae C, Watkins II, et al: A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 15q2. Proc Natl Acad Sci USA 1993; 90:6270-6274.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 6270-6274
-
-
Thierfelder, L.C.1
MacRae, C.2
Watkins, I.I.3
-
23
-
-
0027161005
-
Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11
-
Carrier L, Hengstenberg C, Beckmann JS, et al: Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11. Nature (Genetics) 1993;4:311-313.
-
(1993)
Nature (Genetics)
, vol.4
, pp. 311-313
-
-
Carrier, L.1
Hengstenberg, C.2
Beckmann, J.S.3
-
24
-
-
0029143611
-
Familial hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3
-
MacRae CA, Ghaisas N, Kass S, et al: Familial hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3. J Clin Invest 1995;96:1216-1220.
-
(1995)
J Clin Invest
, vol.96
, pp. 1216-1220
-
-
MacRae, C.A.1
Ghaisas, N.2
Kass, S.3
-
25
-
-
0025295458
-
Complete sequence and organization of the human cardiac ß-myosin heavy chain gene
-
Liew CC, Sole MJ, Yamauchi-Takihara K, et al: Complete sequence and organization of the human cardiac ß-myosin heavy chain gene. Nucleic Acids Res 1990; 18:3647-3651.
-
(1990)
Nucleic Acids Res
, vol.18
, pp. 3647-3651
-
-
Liew, C.C.1
Sole, M.J.2
Yamauchi-Takihara, K.3
-
26
-
-
0022542030
-
Development and functional adaptation of contractile proteins in cardiac and skeletal muscles
-
Swynghedauw B: Development and functional adaptation of contractile proteins in cardiac and skeletal muscles. Physiol Rev 1986;66:710-771.
-
(1986)
Physiol Rev
, vol.66
, pp. 710-771
-
-
Swynghedauw, B.1
-
27
-
-
0028261701
-
Single myosin mechanics: PicoNewton forces and nanometer steps
-
Finer JT, Simmons RM, Spudich JA: Single myosin mechanics: PicoNewton forces and nanometer steps. Nature 1994;368:113-119.
-
(1994)
Nature
, vol.368
, pp. 113-119
-
-
Finer, J.T.1
Simmons, R.M.2
Spudich, J.A.3
-
28
-
-
0028318295
-
Single-molecule analysis of the acto-myosin motor using nano-manipulation
-
Ishijima A, Harada Y, Kojima H, et al: Single-molecule analysis of the acto-myosin motor using nano-manipulation. Biochem Biophys Res Commun 1994;199: 1057-1063.
-
(1994)
Biochem Biophys Res Commun
, vol.199
, pp. 1057-1063
-
-
Ishijima, A.1
Harada, Y.2
Kojima, H.3
-
29
-
-
0027504548
-
Independent origin of identical β cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathy
-
Watkins H, Thierfelder L, Anan R, et al: Independent origin of identical β cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathy. Am J Hum Genet 1993;53:1180-1185.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 1180-1185
-
-
Watkins, H.1
Thierfelder, L.2
Anan, R.3
-
30
-
-
0027138216
-
Familial hypertrophic cardiomyopathy: Microsatellite haplotyping and identification of a hot spot for mutations in the β-myosin heavy chain gene
-
Dausse E, Komajda M, Fetler L, et al: Familial hypertrophic cardiomyopathy: Microsatellite haplotyping and identification of a hot spot for mutations in the β-myosin heavy chain gene. J Clin Invest 1993;92:2807-2813.
-
(1993)
J Clin Invest
, vol.92
, pp. 2807-2813
-
-
Dausse, E.1
Komajda, M.2
Fetler, L.3
-
31
-
-
0028306518
-
719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy
-
719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy. Human Mol Genet 1994;3: 1025-1026.
-
(1994)
Human Mol Genet
, vol.3
, pp. 1025-1026
-
-
Consevage, M.W.1
Salada, G.C.2
Baylen, B.G.3
-
32
-
-
0027070276
-
Detection of a new mutation in the beta myosin heavy chain gene in an individual with hypertrophic cardiomyopathy
-
Marian AJ, Yu QT, Mares A Jr., et al: Detection of a new mutation in the beta myosin heavy chain gene in an individual with hypertrophic cardiomyopathy. J Clin Invest 1992;90:2156-2165.
-
(1992)
J Clin Invest
, vol.90
, pp. 2156-2165
-
-
Marian, A.J.1
Yu, Q.T.2
Mares Jr., A.3
-
33
-
-
0026485701
-
Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations
-
Watkins H, Thierfelder L, Hwang DS, et al: Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations. J Clin Invest 1992;90:1666-1671.
-
(1992)
J Clin Invest
, vol.90
, pp. 1666-1671
-
-
Watkins, H.1
Thierfelder, L.2
Hwang, D.S.3
-
34
-
-
0028109492
-
Isolation of a de novo mutant myocardial βMHC protein in a pedigree with hypertrophic cardiomyopathy
-
Greve G, Bachinski LL, Friedman DL, et al: Isolation of a de novo mutant myocardial βMHC protein in a pedigree with hypertrophic cardiomyopathy. Human Mol Genet 1994;3:2073-2075.
-
(1994)
Human Mol Genet
, vol.3
, pp. 2073-2075
-
-
Greve, G.1
Bachinski, L.L.2
Friedman, D.L.3
-
35
-
-
0027236033
-
Molecular cloning and developmental expression of human cardiac troponin T
-
Mesnard L, Samson F, Espinasse I, et al: Molecular cloning and developmental expression of human cardiac troponin T. FEBS Lett 1993;328:139-144.
-
(1993)
FEBS Lett
, vol.328
, pp. 139-144
-
-
Mesnard, L.1
Samson, F.2
Espinasse, I.3
-
36
-
-
0028302366
-
Human cardiac troponin T: Identification of fetal isoforms and assignment of the TNNT2 locus to chromosome 1q
-
Townsend PJ, Farza H, MacGeon C, et al: Human cardiac troponin T: Identification of fetal isoforms and assignment of the TNNT2 locus to chromosome 1q. Genomics 1994;21:311-316.
-
(1994)
Genomics
, vol.21
, pp. 311-316
-
-
Townsend, P.J.1
Farza, H.2
MacGeon, C.3
-
37
-
-
0028969444
-
Human cardiac troponin T: Cloning and expression of new isoforms in the normal and failing heart
-
Mesnard L, Logeart D, Taviaux S, et al: Human cardiac troponin T: Cloning and expression of new isoforms in the normal and failing heart. Circ Res 1995; 76:687-692.
-
(1995)
Circ Res
, vol.76
, pp. 687-692
-
-
Mesnard, L.1
Logeart, D.2
Taviaux, S.3
-
38
-
-
0028943382
-
Molecular basis of human cardiac troponin T isoforms expressed in the developing, adult, and failing heart
-
Anderson PAW, Greig A, Mark TM, et al: Molecular basis of human cardiac troponin T isoforms expressed in the developing, adult, and failing heart. Circ Res 1995;76:681-686.
-
(1995)
Circ Res
, vol.76
, pp. 681-686
-
-
Anderson, P.A.W.1
Greig, A.2
Mark, T.M.3
-
39
-
-
0029031198
-
The troponin complex and regulation of muscle contraction
-
Farah CS, Reinach FC: The troponin complex and regulation of muscle contraction. FASEB J 1995;9:755-767.
-
(1995)
FASEB J
, vol.9
, pp. 755-767
-
-
Farah, C.S.1
Reinach, F.C.2
-
40
-
-
0028902929
-
Mutations in the genes for cardiac troponin T and α-tropomyosin in hypertrophic cardiomyopathy
-
Watkins H, McKenna WJ, Thierfelder L, et al: Mutations in the genes for cardiac troponin T and α-tropomyosin in hypertrophic cardiomyopathy. N Engl J Med 1995;332:1058-1064.
-
(1995)
N Engl J Med
, vol.332
, pp. 1058-1064
-
-
Watkins, H.1
McKenna, W.J.2
Thierfelder, L.3
-
41
-
-
8044244822
-
Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy
-
Forissier J-F, Carrier L, Farza H, et al: Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy. Circulation 1996;94:3096-3073.
-
(1996)
Circulation
, vol.94
, pp. 3096-13073
-
-
Forissier, J.-F.1
Carrier, L.2
Farza, H.3
-
42
-
-
0023071735
-
Structural aspects of troponin-tropomyosin regulation of skeletal muscle contraction
-
Zot AS, Potter JD: Structural aspects of troponin-tropomyosin regulation of skeletal muscle contraction. Annu Rev Biophys Chem 1987;16:535-559.
-
(1987)
Annu Rev Biophys Chem
, vol.16
, pp. 535-559
-
-
Zot, A.S.1
Potter, J.D.2
-
43
-
-
0028954656
-
A de novo mutation in a tropomyosin that causes hypertrophic cardiomyopathy
-
Watkins H, Anan R, Coviello DA, et al: A de novo mutation in a tropomyosin that causes hypertrophic cardiomyopathy. Circulation 1995;91:2302-2305.
-
(1995)
Circulation
, vol.91
, pp. 2302-2305
-
-
Watkins, H.1
Anan, R.2
Coviello, D.A.3
-
44
-
-
0030052266
-
A molecular map of the interactions between titin and myosin-binding protein C: Implications for sarcomeric assembly in familial hypertrophic cardiomyopathy
-
Freiburg A, Gautel M: A molecular map of the interactions between titin and myosin-binding protein C: Implications for sarcomeric assembly in familial hypertrophic cardiomyopathy. Eur J Biochem 1996;235: 317-323.
-
(1996)
Eur J Biochem
, vol.235
, pp. 317-323
-
-
Freiburg, A.1
Gautel, M.2
-
45
-
-
0031002460
-
Folding-unfolding transitions in single titin molecules characterized with laser tweezers
-
Kellermayer MSZ, Smith SB, Granzier HL, et al: Folding-unfolding transitions in single titin molecules characterized with laser tweezers. Science 1997;276:1112-1116.
-
(1997)
Science
, vol.276
, pp. 1112-1116
-
-
Kellermayer, M.S.Z.1
Smith, S.B.2
Granzier, H.L.3
-
46
-
-
0031055854
-
Organization and sequence of human cardiac myosin binding protein C gene (MyBPCS) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy
-
Carrier L, Bonne G, Bahrend E, et al: Organization and sequence of human cardiac myosin binding protein C gene (MyBPCS) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy. Circ Res 1997;80:427-434.
-
(1997)
Circ Res
, vol.80
, pp. 427-434
-
-
Carrier, L.1
Bonne, G.2
Bahrend, E.3
-
47
-
-
0029029027
-
Phosphorylation switches specific for the cardiac isoform of myosin binding protein-C: A modulator of cardiac contraction?
-
Gautel M, Zuffardi O, Freiburg A, et al: Phosphorylation switches specific for the cardiac isoform of myosin binding protein-C: A modulator of cardiac contraction? EMBO J 1995;14:1952-1960.
-
(1995)
EMBO J
, vol.14
, pp. 1952-1960
-
-
Gautel, M.1
Zuffardi, O.2
Freiburg, A.3
-
48
-
-
0030852878
-
Novel splice donor site mutation in the cardiac myosin-binding protein-C gene in familial hypertrophic cardiomyopathy. Characterization of cardiac transcript and protein
-
Rottbauer W, Gautel M, Zehelein J, et al: Novel splice donor site mutation in the cardiac myosin-binding protein-C gene in familial hypertrophic cardiomyopathy. Characterization of cardiac transcript and protein. J Clin Invest 1997;100:475-482.
-
(1997)
J Clin Invest
, vol.100
, pp. 475-482
-
-
Rottbauer, W.1
Gautel, M.2
Zehelein, J.3
-
49
-
-
0027426228
-
Skeletal muscle myosin light chains are essential for physiological speeds of shortening
-
Lowey S, Waller GS, Trybus KM: Skeletal muscle myosin light chains are essential for physiological speeds of shortening. Nature 1993;365:454-456.
-
(1993)
Nature
, vol.365
, pp. 454-456
-
-
Lowey, S.1
Waller, G.S.2
Trybus, K.M.3
-
50
-
-
0030038230
-
Regulation of human heart contractility by essential myosin light chain isoforms
-
Morano M, Zacharzowski U, Maier M, et al: Regulation of human heart contractility by essential myosin light chain isoforms. J Clin Invest 1996;98:467-473.
-
(1996)
J Clin Invest
, vol.98
, pp. 467-473
-
-
Morano, M.1
Zacharzowski, U.2
Maier, M.3
-
51
-
-
0030892526
-
Transgenic remodeling of the regulatory light chains in the mammalian heart
-
Gulick J, Hewettt TE, Klevitsky R, et al: Transgenic remodeling of the regulatory light chains in the mammalian heart. Circ Res 1997;80:655-664.
-
(1997)
Circ Res
, vol.80
, pp. 655-664
-
-
Gulick, J.1
Hewettt, T.E.2
Klevitsky, R.3
-
52
-
-
0027300234
-
Myosin light chain phosphorylation in vertebrate striated muscle: Regulation and function
-
Sweeney HL, Bowmann BF, Stull JT: Myosin light chain phosphorylation in vertebrate striated muscle: Regulation and function. Am J Physiol 1993;264: C1085-C1095.
-
(1993)
Am J Physiol
, vol.264
-
-
Sweeney, H.L.1
Bowmann, B.F.2
Stull, J.T.3
-
53
-
-
0028926032
-
Impairment of muscle function caused by mutations of phosphorylation sites in myosin regulatory light chain
-
Tohtong R, Yamashita H, Graham M, et al: Impairment of muscle function caused by mutations of phosphorylation sites in myosin regulatory light chain. Nature 1995;374:650-653.
-
(1995)
Nature
, vol.374
, pp. 650-653
-
-
Tohtong, R.1
Yamashita, H.2
Graham, M.3
-
54
-
-
0029641633
-
Mapping TNNCI, the gene that encodes cardiac troponin I in the human and mouse
-
Bermingham N. Mapping TNNCI, the gene that encodes cardiac troponin I in the human and mouse. Genomics 1995;30:620-622.
-
(1995)
Genomics
, vol.30
, pp. 620-622
-
-
Bermingham, N.1
-
55
-
-
0018103817
-
"Malignant" hypertrophic cardiomyopathy: Identification of a subgroup of families with unusually frequent premature death
-
Maron BJ, Lipson LC, Roberts WC, et al: "Malignant" hypertrophic cardiomyopathy: Identification of a subgroup of families with unusually frequent premature death. Am J Cardiol 1978;41:1133-1140.
-
(1978)
Am J Cardiol
, vol.41
, pp. 1133-1140
-
-
Maron, B.J.1
Lipson, L.C.2
Roberts, W.C.3
-
56
-
-
0031114657
-
Prognostic significance of β-myosin heavy chain mutations is reflective of their hypertrophic expressivity in patients with hypertrophic cardiomyopathy
-
Abchee A, Marian AJ: Prognostic significance of β-myosin heavy chain mutations is reflective of their hypertrophic expressivity in patients with hypertrophic cardiomyopathy. J Invest Med 1997;45:191-196.
-
(1997)
J Invest Med
, vol.45
, pp. 191-196
-
-
Abchee, A.1
Marian, A.J.2
-
57
-
-
0027425610
-
Angiotensin converting enzyme polymorphism is associated with hypertrophic cardiomyopathy as well as sudden cardiac death
-
Marian AJ, Yu Q-T, Workman R, et al: Angiotensin converting enzyme polymorphism is associated with hypertrophic cardiomyopathy as well as sudden cardiac death. Lancet 1993;342:1073-1074.
-
(1993)
Lancet
, vol.342
, pp. 1073-1074
-
-
Marian, A.J.1
Yu, Q.-T.2
Workman, R.3
-
58
-
-
0029149023
-
Angiotensin 1 converting enzyme genotypes influence the phenotypic expression of hypertrophic cardiomyopathy
-
Lechin M, Quinones M, Omran A, et al: Angiotensin 1 converting enzyme genotypes influence the phenotypic expression of hypertrophic cardiomyopathy. Circulation 1995;92:1808-1812.
-
(1995)
Circulation
, vol.92
, pp. 1808-1812
-
-
Lechin, M.1
Quinones, M.2
Omran, A.3
-
60
-
-
0026573969
-
Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy
-
Watkins H, Rosenweig A, Hwang D, et al: Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy. N Engl J Med 1992;326:1108-1114..
-
(1992)
N Engl J Med
, vol.326
, pp. 1108-1114
-
-
Watkins, H.1
Rosenweig, A.2
Hwang, D.3
-
61
-
-
0027954269
-
Prognostic implications of novel β cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy
-
Anan R, Greve G, Thierfelder L, et al: Prognostic implications of novel β cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy. J Clin Invest 1994;93:280-285.
-
(1994)
J Clin Invest
, vol.93
, pp. 280-285
-
-
Anan, R.1
Greve, G.2
Thierfelder, L.3
-
62
-
-
0028935226
-
Sudden death in hypertrophic cardiomyopathy: Genotype-phenotype correlation of beta myosin heavy chain mutations
-
Marian AJ, Mares A, Kelley D, et al: Sudden death in hypertrophic cardiomyopathy: Genotype-phenotype correlation of beta myosin heavy chain mutations. Eur Heart J 1995;16:368-376.
-
(1995)
Eur Heart J
, vol.16
, pp. 368-376
-
-
Marian, A.J.1
Mares, A.2
Kelley, D.3
-
64
-
-
0028140230
-
Genotype-phenotype correlations in hypertrophic cardiomyopathy: Insights provided by comparisons of kindreds with distinct and identical β-myosin heavy chain gene mutations
-
Fananapazir L, Epstein ND: Genotype-phenotype correlations in hypertrophic cardiomyopathy: Insights provided by comparisons of kindreds with distinct and identical β-myosin heavy chain gene mutations. Circulation 1994;89:22-32.
-
(1994)
Circulation
, vol.89
, pp. 22-32
-
-
Fananapazir, L.1
Epstein, N.D.2
-
65
-
-
0028911948
-
Sudden cardiac death in hypertrophic cardiomyopathy: From bench to bedside with an emphasis on genetic markers
-
Marian AJ: Sudden cardiac death in hypertrophic cardiomyopathy: From bench to bedside with an emphasis on genetic markers. Clin Cardiol 1994;18: 189-198.
-
(1994)
Clin Cardiol
, vol.18
, pp. 189-198
-
-
Marian, A.J.1
-
67
-
-
0031042881
-
Clinical feature of hypertrophic cardiomyopathy caused by mutations of a "hot spot" in the alpha-tropomyosin gene
-
Coviello DA, Maron BJ, Spirito P, et al: Clinical feature of hypertrophic cardiomyopathy caused by mutations of a "hot spot" in the alpha-tropomyosin gene. J Am Coll Cardiol 1997;29:635-640.
-
(1997)
J Am Coll Cardiol
, vol.29
, pp. 635-640
-
-
Coviello, D.A.1
Maron, B.J.2
Spirito, P.3
-
68
-
-
0027302431
-
Skeletal muscle expression and abnormal function of beta myosin in hypertrophic cardiomyopathy
-
Cuda G, Fananapazir L, Zhu W, et al: Skeletal muscle expression and abnormal function of beta myosin in hypertrophic cardiomyopathy. J Clin Invest 1993;91: 2861-2865.
-
(1993)
J Clin Invest
, vol.91
, pp. 2861-2865
-
-
Cuda, G.1
Fananapazir, L.2
Zhu, W.3
-
69
-
-
0027980111
-
Heterologous expression of a cardiomyopathic myosin that is defective in its actin interaction
-
Sweeney HL, Straceski AJ, Leinwand LA, et al: Heterologous expression of a cardiomyopathic myosin that is defective in its actin interaction. J Biol Chem 1994; 269:1603-1605.
-
(1994)
J Biol Chem
, vol.269
, pp. 1603-1605
-
-
Sweeney, H.L.1
Straceski, A.J.2
Leinwand, L.A.3
-
70
-
-
0028967729
-
Abnormal contractile properties of muscle fibers expressing β-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy
-
Lankford EB, Epstein ND, Fananapazir L, et al: Abnormal contractile properties of muscle fibers expressing β-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy. J Clin Invest 1995; 95:1409-1414.
-
(1995)
J Clin Invest
, vol.95
, pp. 1409-1414
-
-
Lankford, E.B.1
Epstein, N.D.2
Fananapazir, L.3
-
71
-
-
0028088987
-
Functional analysis of myosin missense mutations in familial hypertrophic cardiomyopathy
-
Straceski AJ, Geisterfer-Lowrance A, Seidman CE, et al: Functional analysis of myosin missense mutations in familial hypertrophic cardiomyopathy. Proc Natl Acad Sci USA 1994;91:589-593.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 589-593
-
-
Straceski, A.J.1
Geisterfer-Lowrance, A.2
Seidman, C.E.3
-
72
-
-
0029029473
-
Expression of the mutation causing hypertrophic cardiomyopathy disrupts sarcomere assembly in adult feline cardiac myocytes
-
Marian AJ, Yu Q-T, Mann D, et al: Expression of the mutation causing hypertrophic cardiomyopathy disrupts sarcomere assembly in adult feline cardiac myocytes. Circ Res 1995;77:98-106.
-
(1995)
Circ Res
, vol.77
, pp. 98-106
-
-
Marian, A.J.1
Yu, Q.-T.2
Mann, D.3
-
73
-
-
0031030298
-
Electrophysiological abnormalities and arrhythmias in αMHC mutant familial hypertrophic cardiomyopathy in mice
-
Berul CL, Christe ME, Aronovitz MJ, et al: Electrophysiological abnormalities and arrhythmias in αMHC mutant familial hypertrophic cardiomyopathy in mice. J Clin Invest 1997;99:570-576.
-
(1997)
J Clin Invest
, vol.99
, pp. 570-576
-
-
Berul, C.L.1
Christe, M.E.2
Aronovitz, M.J.3
-
74
-
-
0029807438
-
Mice expressing mutant myosin heavy chains are a model for familial hypertrophic cardiomyopathy
-
Vikstrom KL, Factor SM, Leinwand LA: Mice expressing mutant myosin heavy chains are a model for familial hypertrophic cardiomyopathy. Mol Med 1996; 2:556-567.
-
(1996)
Mol Med
, vol.2
, pp. 556-567
-
-
Vikstrom, K.L.1
Factor, S.M.2
Leinwand, L.A.3
-
75
-
-
0029993918
-
Altered cardiac troponin T in vitro function in the presence of a mutation implicated in familial hypertrophic cardiomyopathy
-
Lin D, Bobkova A, Homsher E, et al: Altered cardiac troponin T in vitro function in the presence of a mutation implicated in familial hypertrophic cardiomyopathy. J Clin Invest 1996;97:2842-2848.
-
(1996)
J Clin Invest
, vol.97
, pp. 2842-2848
-
-
Lin, D.1
Bobkova, A.2
Homsher, E.3
-
76
-
-
0029804760
-
Expression and functional assessment of a truncated cardiac troponin T that causes hypertrophic cardiomyopathy. Evidence for a dominant negative action
-
Watkins H, Seidman CE, Seidman JG, et al: Expression and functional assessment of a truncated cardiac troponin T that causes hypertrophic cardiomyopathy. Evidence for a dominant negative action. J Clin Invest 1996;98:2456-2461.
-
(1996)
J Clin Invest
, vol.98
, pp. 2456-2461
-
-
Watkins, H.1
Seidman, C.E.2
Seidman, J.G.3
-
77
-
-
0030611676
-
92Gln) human cardiac troponin T, known to cause hypertrophic cardiomyopathy, impairs adult cardiac myocytes contractility
-
92Gln) human cardiac troponin T, known to cause hypertrophic cardiomyopathy, impairs adult cardiac myocytes contractility. Circ Res 1997;81;76-85.
-
(1997)
Circ Res
, vol.81
, pp. 76-85
-
-
Marian, A.J.1
Zhao, G.2
Seta, Y.3
-
78
-
-
0030933128
-
Effects of two familial hypertrophic cardiomyopathy-causing mutations on α-tropomyosin structure and function
-
Golistina N, An Y, Greenfield NJ, et al: Effects of two familial hypertrophic cardiomyopathy-causing mutations on α-tropomyosin structure and function. Biochemistry 1997;36:4637-4642.
-
(1997)
Biochemistry
, vol.36
, pp. 4637-4642
-
-
Golistina, N.1
An, Y.2
Greenfield, N.J.3
-
79
-
-
0027299865
-
Increased nuclear protooncogene expression in hypertrophic cardiomyopathy
-
Hengstenberg C, Maisch B: Increased nuclear protooncogene expression in hypertrophic cardiomyopathy. Cardioscience 1993;1:15-20.
-
(1993)
Cardioscience
, vol.1
, pp. 15-20
-
-
Hengstenberg, C.1
Maisch, B.2
-
80
-
-
0026455138
-
Plasma levels of atrial natriuretic peptide in hypertrophic cardiomyopathy
-
Derchi G, Bellone P, Chiarella F, et al: Plasma levels of atrial natriuretic peptide in hypertrophic cardiomyopathy. Am J Cardiol 1992;70:1502-1504.
-
(1992)
Am J Cardiol
, vol.70
, pp. 1502-1504
-
-
Derchi, G.1
Bellone, P.2
Chiarella, F.3
-
81
-
-
0027255523
-
Ventricular expression of brain natriuretic peptide in hypertrophic cardiomyopathy
-
Hasegawa K, Fujiwara H, Doyama K, et al: Ventricular expression of brain natriuretic peptide in hypertrophic cardiomyopathy. Circulation 1993;88:372-380.
-
(1993)
Circulation
, vol.88
, pp. 372-380
-
-
Hasegawa, K.1
Fujiwara, H.2
Doyama, K.3
-
82
-
-
0030877545
-
Overexpression of transforming growth factor-β1 and insulin-like growth factor-1 in patients with idiopathic hypertrophic cardiomyopathy
-
Li R-K, Li G, Mickle DAG, et al: Overexpression of transforming growth factor-β1 and insulin-like growth factor-1 in patients with idiopathic hypertrophic cardiomyopathy. Circulation 1997;96:874-881.
-
(1997)
Circulation
, vol.96
, pp. 874-881
-
-
Li, R.-K.1
Li, G.2
Mickle, D.A.G.3
-
83
-
-
10244221064
-
Ablation of the murine α myosin heavy chain gene leads to dosage effects and functional deficits in the heart
-
Jones WK, Grupp IL, Doetschman T, et al: Ablation of the murine α myosin heavy chain gene leads to dosage effects and functional deficits in the heart. J Clin Invest 1996;98:1906-1917.
-
(1996)
J Clin Invest
, vol.98
, pp. 1906-1917
-
-
Jones, W.K.1
Grupp, I.L.2
Doetschman, T.3
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