-
1
-
-
0014103605
-
ATPase activity of myosin correlated with speed of muscle shortening
-
Barany M. ATPase activity of myosin correlated with speed of muscle shortening. J Gen Physiol. 50(Suppl):1967;197-218.
-
(1967)
J Gen Physiol
, vol.50
, Issue.SUPPL.
, pp. 197-218
-
-
Barany, M.1
-
2
-
-
0032555955
-
Familial hypertrophic cardiomyopathy: From mutations to functional defects
-
Bonne G., Carrier L., Richard P.et al. Familial hypertrophic cardiomyopathy. from mutations to functional defects Circ Res. 83:1998;580-593.
-
(1998)
Circ Res
, vol.83
, pp. 580-593
-
-
Bonne, G.1
Carrier, L.2
Richard, P.3
-
3
-
-
0030853711
-
Pathogenesis and treatment of sickle cell disease
-
Bunn F.H. Pathogenesis and treatment of sickle cell disease. N Engl J Med. 337:1997;762-769.
-
(1997)
N Engl J Med
, vol.337
, pp. 762-769
-
-
Bunn, F.H.1
-
4
-
-
0030976860
-
The in vitro motility activity of β-cardiac myosin depends on the nature of the β-myosin heavy chain gene mutation in hypertrophic cardiomyopathy
-
Cuda G., Fananapazir L., Epstein N.D., Sellers J.R. The in vitro motility activity of β-cardiac myosin depends on the nature of the β-myosin heavy chain gene mutation in hypertrophic cardiomyopathy. J Muscle Res Cell Motil. 18:1997;275-283.
-
(1997)
J Muscle Res Cell Motil
, vol.18
, pp. 275-283
-
-
Cuda, G.1
Fananapazir, L.2
Epstein, N.D.3
Sellers, J.R.4
-
5
-
-
0027302431
-
Skeletal muscle expression and abnormal function of β-myosin in hypertrophic cardiomyopathy
-
Cuda G., Fananapazir L., Zhu W.-S.et al. Skeletal muscle expression and abnormal function of β-myosin in hypertrophic cardiomyopathy. J Clin Invest. 91:1993;2861-2865.
-
(1993)
J Clin Invest
, vol.91
, pp. 2861-2865
-
-
Cuda, G.1
Fananapazir, L.2
Zhu, W.-S.3
-
6
-
-
0032483563
-
Crystal structure of a vertebrate smooth muscle myosin motor domain and its complex with the essential light chain: Visualization of the pre-power stroke state
-
Dominguez R., Freyzon Y., Trybus K.M., Cohen C. Crystal structure of a vertebrate smooth muscle myosin motor domain and its complex with the essential light chain. visualization of the pre-power stroke state Cell. 94:1998;559-571.
-
(1998)
Cell
, vol.94
, pp. 559-571
-
-
Dominguez, R.1
Freyzon, Y.2
Trybus, K.M.3
Cohen, C.4
-
8
-
-
0030899032
-
Characterization of mutant myosins of Dictyostelium discoideum equivalent to human familial hypertrophic cardiomyopathy mutants
-
Fujita H., Sugiura S., Monomura S.et al. Characterization of mutant myosins of Dictyostelium discoideum equivalent to human familial hypertrophic cardiomyopathy mutants. J Clin Invest. 99:1997;1010-1015.
-
(1997)
J Clin Invest
, vol.99
, pp. 1010-1015
-
-
Fujita, H.1
Sugiura, S.2
Monomura, S.3
-
9
-
-
0032883413
-
Structural mechanism of muscle contraction
-
Geeves M.A., Holmes K.C. Structural mechanism of muscle contraction. Annu Rev Biochem. 68:1999;687-728.
-
(1999)
Annu Rev Biochem
, vol.68
, pp. 687-728
-
-
Geeves, M.A.1
Holmes, K.C.2
-
10
-
-
0030067394
-
A mouse model of familial hypertrophic cardiomyopathy
-
Geisterfer-Lowrance A.A., Christe M., Conner D.A.et al. A mouse model of familial hypertrophic cardiomyopathy. Science. 272:1996;731-734.
-
(1996)
Science
, vol.272
, pp. 731-734
-
-
Geisterfer-Lowrance, A.A.1
Christe, M.2
Conner, D.A.3
-
11
-
-
0025040392
-
A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation
-
Geisterfer-Lowrance A.A., Kass S., Tanigawa G.et al. A molecular basis for familial hypertrophic cardiomyopathy. a β cardiac myosin heavy chain gene missense mutation Cell. 62:1990;999-1006.
-
(1990)
Cell
, vol.62
, pp. 999-1006
-
-
Geisterfer-Lowrance, A.A.1
Kass, S.2
Tanigawa, G.3
-
12
-
-
0024332141
-
Dystrophin abnormalities in Duchenne/Becker muscular dystrophy
-
Hoffman E., Kunkel L.M. Dystrophin abnormalities in Duchenne/Becker muscular dystrophy. Neuron. 2:1989;1019-1029.
-
(1989)
Neuron
, vol.2
, pp. 1019-1029
-
-
Hoffman, E.1
Kunkel, L.M.2
-
13
-
-
0014685163
-
The mechanism of muscle contraction
-
Huxley H.E. The mechanism of muscle contraction. Science. 164:1969;1356-1366.
-
(1969)
Science
, vol.164
, pp. 1356-1366
-
-
Huxley, H.E.1
-
14
-
-
0033386313
-
A transgenic rabbit model for human hypertrophic cardiomyopathy
-
Marian A.J., Wu Y., Lim D.-S.et al. A transgenic rabbit model for human hypertrophic cardiomyopathy. J Clin Invest. 104:1999;1683-1692.
-
(1999)
J Clin Invest
, vol.104
, pp. 1683-1692
-
-
Marian, A.J.1
Wu, Y.2
Lim, D.-S.3
-
15
-
-
0029029473
-
Expression of a mutation causing hypertrophic cardiomyopathy disrupts sarcomere assembly in adult feline cardiac myocytes
-
Marian A.J., Yu Q.-T., Mann D.L.et al. Expression of a mutation causing hypertrophic cardiomyopathy disrupts sarcomere assembly in adult feline cardiac myocytes. Circ Res. 77:1995;98-106.
-
(1995)
Circ Res
, vol.77
, pp. 98-106
-
-
Marian, A.J.1
Yu, Q.-T.2
Mann, D.L.3
-
16
-
-
0024785576
-
Full length rat alpha and beta cardiac myosin heavy chain sequences
-
McNally E.M., Kraft R., Bravo-Zehnder M.et al. Full length rat alpha and beta cardiac myosin heavy chain sequences. J Mol Biol. 210:1989;665-671.
-
(1989)
J Mol Biol
, vol.210
, pp. 665-671
-
-
McNally, E.M.1
Kraft, R.2
Bravo-Zehnder, M.3
-
17
-
-
0033799445
-
Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy
-
Olson T.M., Doan T.P., Kishimoto N.Y.et al. Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy. J Mol Cell Cardiol. 32:2000;1687-1694.
-
(2000)
J Mol Cell Cardiol
, vol.32
, pp. 1687-1694
-
-
Olson, T.M.1
Doan, T.P.2
Kishimoto, N.Y.3
-
18
-
-
0034494362
-
R403Q and L908V mutant β-cardiac myosin from patients with familial hypertrophy cardiomyopathy exhibit enhanced mechanical performance at the single molecule level
-
Palmiter K.A., Tyska M.J., Haeberle J.R.et al. R403Q and L908V mutant β-cardiac myosin from patients with familial hypertrophy cardiomyopathy exhibit enhanced mechanical performance at the single molecule level. J Muscle Res Cell Motil. 21:2000;609-620.
-
(2000)
J Muscle Res Cell Motil
, vol.21
, pp. 609-620
-
-
Palmiter, K.A.1
Tyska, M.J.2
Haeberle, J.R.3
-
19
-
-
0029024879
-
Structural interpretation of the mutations in the β-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy
-
Rayment I., Holden H.M., Sellers J.R.et al. Structural interpretation of the mutations in the β-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy. Proc Natl Acad Sci USA. 92:1995;3864-3868.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 3864-3868
-
-
Rayment, I.1
Holden, H.M.2
Sellers, J.R.3
-
20
-
-
0027226230
-
Structure of the actin-myosin complex and its implications for muscle contraction
-
a
-
Rayment I., Holden H.M., Whittaker M.et al. Structure of the actin-myosin complex and its implications for muscle contraction. Science. 261:1993;58-65. a.
-
(1993)
Science
, vol.261
, pp. 58-65
-
-
Rayment, I.1
Holden, H.M.2
Whittaker, M.3
-
21
-
-
0027194702
-
Three-dimensional structure of myosin subfragment-1: A molecular motor
-
b
-
Rayment I., Rypniewski W.R., Schmidt-Base K.et al. Three-dimensional structure of myosin subfragment-1. a molecular motor Science. 261:1993;50-58. b.
-
(1993)
Science
, vol.261
, pp. 50-58
-
-
Rayment, I.1
Rypniewski, W.R.2
Schmidt-Base, K.3
-
22
-
-
0031794853
-
Functional analysis of myosin mutations that cause familial hypertrophic cardiomyopathy
-
Roopnarine O., Leinwand L.A. Functional analysis of myosin mutations that cause familial hypertrophic cardiomyopathy. Biophys J. 75:1998;3023-3030.
-
(1998)
Biophys J
, vol.75
, pp. 3023-3030
-
-
Roopnarine, O.1
Leinwand, L.A.2
-
23
-
-
0030454149
-
Functional analysis of the mutations in the human cardiac β-myosin that are responsible for familial hypertrophic cardiomyopathy
-
Sata M., Ikebe M. Functional analysis of the mutations in the human cardiac β-myosin that are responsible for familial hypertrophic cardiomyopathy. J Clin Invest. 98:1996;2866-2873.
-
(1996)
J Clin Invest
, vol.98
, pp. 2866-2873
-
-
Sata, M.1
Ikebe, M.2
-
24
-
-
0027980111
-
Heterologous expression of a cardiomyopathic myosin that is defective in its actin interaction
-
Sweeney H.L., Straceski A.J., Leinwand L.A.et al. Heterologous expression of a cardiomyopathic myosin that is defective in its actin interaction. J Biol Chem. 269:1994;1603-1605.
-
(1994)
J Biol Chem
, vol.269
, pp. 1603-1605
-
-
Sweeney, H.L.1
Straceski, A.J.2
Leinwand, L.A.3
-
25
-
-
0034095174
-
Expression of the β (slow)-isoform of MHC in the adult mouse heart causes dominant-negative functional effects
-
Tardiff J.C., Hewett T.E., Factor S.M.et al. Expression of the β (slow)-isoform of MHC in the adult mouse heart causes dominant-negative functional effects. Am J Physiol Heart Circ Physiol. 278:2000;H412-H419.
-
(2000)
Am J Physiol Heart Circ Physiol
, vol.278
, pp. 412-H419
-
-
Tardiff, J.C.1
Hewett, T.E.2
Factor, S.M.3
-
26
-
-
0034646743
-
Single-molecule mechanics of R403Q cardiac myosin isolated from the mouse model of familial hypertrophic cardiomyopathy
-
Tyska M.J., Hayes E., Giewat M.et al. Single-molecule mechanics of R403Q cardiac myosin isolated from the mouse model of familial hypertrophic cardiomyopathy. Circ Res. 86:2000;737-744.
-
(2000)
Circ Res
, vol.86
, pp. 737-744
-
-
Tyska, M.J.1
Hayes, E.2
Giewat, M.3
-
27
-
-
0028983138
-
Cardiac V1 and V3 myosins differ in their hydrolytic and mechanical activities in vitro
-
VanBuren P., Harris D.E., Alpert N.R., Warshaw D.M. Cardiac V1 and V3 myosins differ in their hydrolytic and mechanical activities in vitro. Circ Res. 77:1995;439-444.
-
(1995)
Circ Res
, vol.77
, pp. 439-444
-
-
VanBuren, P.1
Harris, D.E.2
Alpert, N.R.3
Warshaw, D.M.4
-
28
-
-
0030046902
-
Contractile protein mutations and heart disease
-
Vikstrom K.L., Leinwand L.L. Contractile protein mutations and heart disease. Curr Opin Cell Biol. 8:1996;97-105.
-
(1996)
Curr Opin Cell Biol
, vol.8
, pp. 97-105
-
-
Vikstrom, K.L.1
Leinwand, L.L.2
-
29
-
-
0033669710
-
Evidence for cleft closure in actomyosin upon ADP release
-
Volkmann N., Hanein D., Ouyang G.et al. Evidence for cleft closure in actomyosin upon ADP release. Nature Struct Biol. 7:2000;1147-1155.
-
(2000)
Nature Struct Biol
, vol.7
, pp. 1147-1155
-
-
Volkmann, N.1
Hanein, D.2
Ouyang, G.3
-
30
-
-
0026474712
-
Accumulation and assembly of myosin in hypertrophic cardiomyopathy with the 403 Arg to Gln β-myosin heavy chain mutation
-
Vybiral T., Deitiker P.R., Roberts R., Epstein H.F. Accumulation and assembly of myosin in hypertrophic cardiomyopathy with the 403 Arg to Gln β-myosin heavy chain mutation. Circ Res. 71:1992;1404-1409.
-
(1992)
Circ Res
, vol.71
, pp. 1404-1409
-
-
Vybiral, T.1
Deitiker, P.R.2
Roberts, R.3
Epstein, H.F.4
-
31
-
-
0039470294
-
The in vitro motility assay: A window into the myosin molecular motor
-
Warshaw D.M. The in vitro motility assay. a window into the myosin molecular motor News Physiol Sci. 11:1996;1-7.
-
(1996)
News Physiol Sci
, vol.11
, pp. 1-7
-
-
Warshaw, D.M.1
-
32
-
-
0025335344
-
Smooth muscle myosin cross-bridge interactions modulate actin filament sliding velocity in vitro.
-
Warshaw D.M., Desrosiers J.M., Work S.S., Trybus K.M. Smooth muscle myosin cross-bridge interactions modulate actin filament sliding velocity in vitro. J Cell Biol. 111:1990;453-463.
-
(1990)
J Cell Biol
, vol.111
, pp. 453-463
-
-
Warshaw, D.M.1
Desrosiers, J.M.2
Work, S.S.3
Trybus, K.M.4
-
33
-
-
0034623233
-
Functional consequences of mutations in the smooth muscle myosin heavy chain at sites implicated in familial hypertrophic cardiomyopathy
-
Yamashita H., Tyska M.J., Warshaw D.M.et al. Functional consequences of mutations in the smooth muscle myosin heavy chain at sites implicated in familial hypertrophic cardiomyopathy. J Biol Chem. 275:2000;28,045-28,052.
-
(2000)
J Biol Chem
, vol.275
, pp. 28
-
-
Yamashita, H.1
Tyska, M.J.2
Warshaw, D.M.3
|