-
1
-
-
0014396206
-
Calcium ion and muscle contraction
-
Ebashi, S. and Endo, M. (1968) Calcium ion and muscle contraction. Prog. Biophys. Mol. Biol. 18, 123-183
-
(1968)
Prog. Biophys. Mol. Biol.
, vol.18
, pp. 123-183
-
-
Ebashi, S.1
Endo, M.2
-
2
-
-
0023034376
-
Regulatory and cytoskeletal proteins of vertebrate skeletal muscle
-
Ohtsuki, I., Maruyama, K., and Ebashi, S. (1986) Regulatory and cytoskeletal proteins of vertebrate skeletal muscle. Adv. Protein Chem. 38, 1-67
-
(1986)
Adv. Protein Chem.
, vol.38
, pp. 1-67
-
-
Ohtsuki, I.1
Maruyama, K.2
Ebashi, S.3
-
3
-
-
0025968808
-
Sports-related and non-sports-related sudden cardiac death in young adults
-
Burke, A.P., Farb, A., Virmani, R., Goodin, J., and Smialek, J.E. (1991) Sports-related and non-sports-related sudden cardiac death in young adults. Am. Heart J. 121, 568-575
-
(1991)
Am. Heart J.
, vol.121
, pp. 568-575
-
-
Burke, A.P.1
Farb, A.2
Virmani, R.3
Goodin, J.4
Smialek, J.E.5
-
4
-
-
0024757325
-
Sudden death in hypertrophic cardiomyopathy
-
McKenna, W.J. and Camm, A.J. (1989) Sudden death in hypertrophic cardiomyopathy. Circulation 80, 1489-1492
-
(1989)
Circulation
, vol.80
, pp. 1489-1492
-
-
McKenna, W.J.1
Camm, A.J.2
-
5
-
-
0031052924
-
Sudden death due to troponin T mutations
-
Moolman, J.C., Corfield, V.A., Posen, B., Ngumbela, K., Seidman, C.E., Brink, P.A., and Watkins, H. (1997) Sudden death due to troponin T mutations. J. Am. Coll. Cardiol. 29, 549-555
-
(1997)
J. Am. Coll. Cardiol.
, vol.29
, pp. 549-555
-
-
Moolman, J.C.1
Corfield, V.A.2
Posen, B.3
Ngumbela, K.4
Seidman, C.E.5
Brink, P.A.6
Watkins, H.7
-
6
-
-
0028902929
-
Mutations in the genes for cardiac troponin T and α-tropomyosin in hypertrophic cardiomyopathy
-
Watkins, H., McKenna, W.J., Thierfelder, L., Suk, H.J., Anan, R., O'Donoghue, A., Spirito, P., Matsumori, A., Moravec, C.S., Seidman, J.G., and Seidman, C.E. (1995) Mutations in the genes for cardiac troponin T and α-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
-
7
-
-
0031080070
-
Novel missense mutation in cardiac troponin T gene found in Japanese patient with hypertrophic cardiomyopathy
-
Nakajima-Taniguchi, C., Matsui H., Fujio, Y., Nagata, S., Kishimoto, T., and Yamauchi-Takihara, K. (1997) Novel missense mutation in cardiac troponin T gene found in Japanese patient with hypertrophic cardiomyopathy. J. Mol. Cell Cardiol. 29, 839-843
-
(1997)
J. Mol. Cell Cardiol.
, vol.29
, pp. 839-843
-
-
Nakajima-Taniguchi, C.1
Matsui, H.2
Fujio, Y.3
Nagata, S.4
Kishimoto, T.5
Yamauchi-Takihara, K.6
-
8
-
-
0030765610
-
Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy
-
Kimura, A., Harada, H., Park, J.E., Nishi, H., Satoh, M., Takahashi, M., Hiroi, S., Sasaoka, T., Ohbuchi, N., Nakamura, T., Koyanagi, T., Hwang, T.H., Choo, J.A., Chung, K.S., Hasegawa, A., Nagai, R., Okazaki, O., Nakamura, H., Matsuzaki, M., Sakamoto, T., Toshima, H., Koga, Y., Imaizumi, T., and Sasazuki, T. (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
Satoh, M.5
Takahashi, M.6
Hiroi, S.7
Sasaoka, T.8
Ohbuchi, N.9
Nakamura, T.10
Koyanagi, T.11
Hwang, T.H.12
Choo, J.A.13
Chung, K.S.14
Hasegawa, A.15
Nagai, R.16
Okazaki, O.17
Nakamura, H.18
Matsuzaki, M.19
Sakamoto, T.20
Toshima, H.21
Koga, Y.22
Imaizumi, T.23
Sasazuki, T.24
more..
-
9
-
-
0025040392
-
A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation
-
Geisterfer-Lowrance, A.A.T., Kass, S., Tanigawa, G., Vosberg, H.-P., McKenna, W., Seidman, C.E., and Seidman J.G. (1990) A molecular basis for familial hypertrophic cardiomyopathy: a β cardiac myosin heavy chain gene missense mutation. Cell 62, 999-1006
-
(1990)
Cell
, vol.62
, pp. 999-1006
-
-
Geisterfer-Lowrance, A.A.T.1
Kass, S.2
Tanigawa, G.3
Vosberg, H.-P.4
McKenna, W.5
Seidman, C.E.6
Seidman, J.G.7
-
10
-
-
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., Jiang, H., Hassanzadeh, S., Master, S.R., Chang, A., Dalakas, M.C., Rayment, I., Sellers, J.R., Fananapazir, L., and Epstein, N.D. (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
-
11
-
-
0029164976
-
Novel missense mutation in α-tropomyosin gene found in Japanese patients with hypertrophic cardiomyopathy
-
Nakajima-Taniguchi, C., Matsui H., Nagata, S., Kishimoto, T., and Yamauchi-Takihara, K. (1995) Novel missense mutation in α-tropomyosin gene found in Japanese patients with hypertrophic cardiomyopathy. J. Mol. Cell Cardiol. 27, 2053-2058
-
(1995)
J. Mol. Cell Cardiol.
, vol.27
, pp. 2053-2058
-
-
Nakajima-Taniguchi, C.1
Matsui, H.2
Nagata, S.3
Kishimoto, T.4
Yamauchi-Takihara, K.5
-
12
-
-
0028886136
-
Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy
-
Bonne, G., Carrier, L., Bercovici, J., Cruaud, C., Richard, P., Hainque, B., Gautel, M., Labeit, S., James, M., Beckman, J., Weissenbach, J., Vosberg, H.-P., Fiszman, M., Komajda, M., and Schwartz, K. (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
Beckman, J.10
Weissenbach, J.11
Vosberg, H.-P.12
Fiszman, M.13
Komajda, M.14
Schwartz, K.15
-
13
-
-
0028844204
-
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy
-
Watkins, H., Conner, D., Thierfelder, L., Jarcho, J.A., MacRae, C., McKenna, W.J., Maron, B.J., Seidman J.G., and Seidman C.E. (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
-
-
0031855272
-
Troponin T: Genetics, properties and function
-
Perry, S.V. (1998) Troponin T: genetics, properties and function. J. Muscle Res. Cell Motil. 19, 575-602
-
(1998)
J. Muscle Res. Cell Motil.
, vol.19
, pp. 575-602
-
-
Perry, S.V.1
-
15
-
-
0032564354
-
Functional analyses of troponin T mutations that cause hypertrophic cardiomyopathy: Insights into disease pathogenesis and troponin function
-
Sweeney, H.L., Feng, H.S., Yang, Z., and Watkins, H. (1998) Functional analyses of troponin T mutations that cause hypertrophic cardiomyopathy: Insights into disease pathogenesis and troponin function. Proc. Natl. Acad. Sci. USA 95, 14406-14410
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 14406-14410
-
-
Sweeney, H.L.1
Feng, H.S.2
Yang, Z.3
Watkins, H.4
-
16
-
-
0032532087
-
Dominant-negative effect of a mutant cardiac troponin T on cardiac structure and function in transgenic mice
-
Oberst, L., Zhao, G.L., Brugada, R., Michael, L.H., Entman, M.L., Roberts, R., and Marian, A.J. (1998) Dominant-negative effect of a mutant cardiac troponin T on cardiac structure and function in transgenic mice. J. Clin. Invest. 102, 1498-1505
-
(1998)
J. Clin. Invest.
, vol.102
, pp. 1498-1505
-
-
Oberst, L.1
Zhao, G.L.2
Brugada, R.3
Michael, L.H.4
Entman, M.L.5
Roberts, R.6
Marian, A.J.7
-
17
-
-
0032526155
-
A truncated cardiac troponin T molecule in transgenic mice suggests multiple cellular mechanisms for familial hypertrophic cardiomyopathy
-
Tardiff, J.C., Factor, S.M., Tompkins, B.D., Hewett, T.E., Palmer, B.M., Moore, R.L., Schwartz, S., Robbins, J., and Leinwand, L.A. (1998) A truncated cardiac troponin T molecule in transgenic mice suggests multiple cellular mechanisms for familial hypertrophic cardiomyopathy. J. Clin. Invest. 101, 2800-2811
-
(1998)
J. Clin. Invest.
, vol.101
, pp. 2800-2811
-
-
Tardiff, J.C.1
Factor, S.M.2
Tompkins, B.D.3
Hewett, T.E.4
Palmer, B.M.5
Moore, R.L.6
Schwartz, S.7
Robbins, J.8
Leinwand, L.A.9
-
18
-
-
0032716486
-
Cardiac troponin T mutations result in allele-specific phenotypes in a mouse model for hypertrophic cardiomyopathy
-
Tardiff, J.C., Hewett, T.E., Palmer, B.M., Olsson, C., Factor, S.M., Moore, R.L., Robbins, J., and Leinwand, L.A. (1999) Cardiac troponin T mutations result in allele-specific phenotypes in a mouse model for hypertrophic cardiomyopathy. J. Clin. Invest. 104, 469-481
-
(1999)
J. Clin. Invest.
, vol.104
, pp. 469-481
-
-
Tardiff, J.C.1
Hewett, T.E.2
Palmer, B.M.3
Olsson, C.4
Factor, S.M.5
Moore, R.L.6
Robbins, J.7
Leinwand, L.A.8
-
19
-
-
0032724289
-
Identification of a contractile deficit in adult cardiac myocytes expressing hypertrophic cardiomyopathy-associated mutant troponin T proteins
-
Rust, E.M., Albayya, F.P., and Metzger, J.M. (1999) Identification of a contractile deficit in adult cardiac myocytes expressing hypertrophic cardiomyopathy-associated mutant troponin T proteins. J. Clin. Invest. 103, 1459-1467
-
(1999)
J. Clin. Invest.
, vol.103
, pp. 1459-1467
-
-
Rust, E.M.1
Albayya, F.P.2
Metzger, J.M.3
-
20
-
-
0029993918
-
Altered cardiac troponin T in vitro function in the presence of a mutation implicated in a familial hypertrophic cardiomyopathy
-
Lin, D., Bobkova, A., Homsher, E., and Tobacman, L.S. (1996) Altered cardiac troponin T in vitro function in the presence of a mutation implicated in a familial hypertrophic cardiomyopathy J. Clin. Invest. 97, 2842-2848
-
(1996)
J. Clin. Invest.
, vol.97
, pp. 2842-2848
-
-
Lin, D.1
Bobkova, A.2
Homsher, E.3
Tobacman, L.S.4
-
21
-
-
0029804760
-
Expression and functional assessment of a truncated cardiac troponin T that causes hypertrophic cardiomyopathy. Evidence for a dominant negative action
-
Watkins, H., Seidman, C.E., Seidman, J.G., Feng, H.S., and Sweeney, H.L. (1997) Expression and functional assessment of a truncated cardiac troponin T that causes hypertrophic cardiomyopathy. Evidence for a dominant negative action. J. Clin. Invest. 98, 2456-2461
-
(1997)
J. Clin. Invest.
, vol.98
, pp. 2456-2461
-
-
Watkins, H.1
Seidman, C.E.2
Seidman, J.G.3
Feng, H.S.4
Sweeney, H.L.5
-
22
-
-
0030611676
-
92Gln) human troponin T, known to cause hypertrophic cardiomyopathy, impairs adult cardiac myocyte contractility
-
92Gln) human troponin T, known to cause hypertrophic cardiomyopathy, impairs adult cardiac myocyte contractility. Circ. Res. 81, 76-85
-
(1997)
Circ. Res.
, vol.81
, pp. 76-85
-
-
Marian, A.J.1
Zhao, G.2
Seta, Y.3
Roberts, R.4
Yu, Q.-T.5
-
23
-
-
0033605422
-
2+ sensitization and potentiation of the maximum level of myofibrillar ATPase activity caused by mutations of troponin T found in familial hypertrophic cardiomyopathy
-
2+ sensitization and potentiation of the maximum level of myofibrillar ATPase activity caused by mutations of troponin T found in familial hypertrophic cardiomyopathy. J. Biol. Chem. 274, 8806-8812
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 8806-8812
-
-
Yanaga, F.1
Morimoto, S.2
Ohtsuki, I.3
-
24
-
-
0031873371
-
2+-sensitizing effects of the mutations at Ile-79 and Arg-92 of troponin T in hypertrophic cardiomyopathy
-
2+-sensitizing effects of the mutations at Ile-79 and Arg-92 of troponin T in hypertrophic cardiomyopathy. Am. J. Physiol. 44, C200-C207
-
(1998)
Am. J. Physiol.
, vol.44
-
-
Morimoto, S.1
Yanaga, F.2
Minakami, R.3
Ohtsuki, I.4
-
25
-
-
0032824580
-
Effects of missense mutations Phe110Ile and Glu244Asp in human cardiac troponin T on force generation in skinned cardiac muscle fibers
-
Nakaura, H., Yanaga, F., Ohtsuki, I., and Morimoto, S. (1999) Effects of missense mutations Phe110Ile and Glu244Asp in human cardiac troponin T on force generation in skinned cardiac muscle fibers. J. Biochem. 126, 457-460
-
(1999)
J. Biochem.
, vol.126
, pp. 457-460
-
-
Nakaura, H.1
Yanaga, F.2
Ohtsuki, I.3
Morimoto, S.4
-
26
-
-
0033595110
-
Functional consequences of a carboxyl terminal missense mutation Arg278Cys in human cardiac troponin T
-
Morimoto, S., Nakaura, H., Yanaga, F., and Ohtsuki, I. (1999) Functional consequences of a carboxyl terminal missense mutation Arg278Cys in human cardiac troponin T. Biochem. Biophys. Res. Commun. 261, 79-82
-
(1999)
Biochem. Biophys. Res. Commun.
, vol.261
, pp. 79-82
-
-
Morimoto, S.1
Nakaura, H.2
Yanaga, F.3
Ohtsuki, I.4
-
27
-
-
0032864309
-
Functional changes in troponin T by a splice donor site mutation that causes hypertrophic cardiomyopathy
-
Nakaura, H., Morimoto, S., Yanaga, F., Nakata, M., Nishi, H., Imaizumi, T., and Ohtsuki, I. (1999) Functional changes in troponin T by a splice donor site mutation that causes hypertrophic cardiomyopathy.Am. J. Physiol. 46, C225-C232
-
(1999)
Am. J. Physiol.
, vol.46
-
-
Nakaura, H.1
Morimoto, S.2
Yanaga, F.3
Nakata, M.4
Nishi, H.5
Imaizumi, T.6
Ohtsuki, I.7
-
28
-
-
0020967760
-
Chymotryptic subfragments of troponin T from rabbit skeletal muscle. Interaction with tropomyosin, troponin I, and troponin C
-
Tanokura, M., Tawada, Y., Ono, A., and Ohtsuki, I. (1983) Chymotryptic subfragments of troponin T from rabbit skeletal muscle. Interaction with tropomyosin, troponin I, and troponin C. J. Biochem. 93, 331-337
-
(1983)
J. Biochem.
, vol.93
, pp. 331-337
-
-
Tanokura, M.1
Tawada, Y.2
Ono, A.3
Ohtsuki, I.4
-
30
-
-
0026527731
-
Replacement of troponin components in myofibrils
-
Shiraishi, F., Kambara, M., and Ohtsuki, I. (1992) Replacement of troponin components in myofibrils. J. Biochem. 111, 61-65
-
(1992)
J. Biochem.
, vol.111
, pp. 61-65
-
-
Shiraishi, F.1
Kambara, M.2
Ohtsuki, I.3
-
31
-
-
0026316514
-
Replacement of three troponin components with cardiac troponin components within single glycerinated skeletal muscle fibers
-
Hatakenaka, M. and Ohtsuki, I. (1991) Replacement of three troponin components with cardiac troponin components within single glycerinated skeletal muscle fibers. Biochem. Biophys. Res. Commun. 181, 1022-1027
-
(1991)
Biochem. Biophys. Res. Commun.
, vol.181
, pp. 1022-1027
-
-
Hatakenaka, M.1
Ohtsuki, I.2
-
32
-
-
0026579645
-
2+-activated tension development of single glycerinated rabbit skeletal musde fibers
-
2+-activated tension development of single glycerinated rabbit skeletal musde fibers. Eur. J. Biochem. 205, 985-993
-
(1992)
Eur. J. Biochem.
, vol.205
, pp. 985-993
-
-
Hatakenaka, M.1
Ohtsuki, I.2
-
33
-
-
0028969444
-
Human cardiac troponin T: Cloning and expression of new isoforms in the neonatal and failing heart
-
Mesnard, L., Logeart, D., Taviaux, S., Diriong, S., Mercadier, J.-J., and Samson, F. (1995) Human cardiac troponin T: cloning and expression of new isoforms in the neonatal and failing heart. Circ. Res. 76, 687-692
-
(1995)
Circ. Res.
, vol.76
, pp. 687-692
-
-
Mesnard, L.1
Logeart, D.2
Taviaux, S.3
Diriong, S.4
Mercadier, J.-J.5
Samson, F.6
-
34
-
-
0000416248
-
In vitro recombination and mutagenesis of DNA: SOEing together tailor-made genes
-
Horton, R.M. (1993) In vitro recombination and mutagenesis of DNA: SOEing together tailor-made genes. Methods Mol. Biol. 15, 251-261
-
(1993)
Methods Mol. Biol.
, vol.15
, pp. 251-261
-
-
Horton, R.M.1
-
35
-
-
0015213029
-
The purification of cardiac myofibrils with triton X-100
-
Solaro, R.J., Pang, D.C., and Briggs, F.N. (1971) The purification of cardiac myofibrils with triton X-100. Biochim. Biophys. Acta 245, 259-262
-
(1971)
Biochim. Biophys. Acta
, vol.245
, pp. 259-262
-
-
Solaro, R.J.1
Pang, D.C.2
Briggs, F.N.3
-
36
-
-
0019830545
-
A new and convenient colorimetric determination of inorganic orthophosphate and its application to the assay of inorganic pyrophosphatase
-
Heinonen, J.K. and Lahti, R.J. (1981) A new and convenient colorimetric determination of inorganic orthophosphate and its application to the assay of inorganic pyrophosphatase. Anal. Biochem. 113, 313-317
-
(1981)
Anal. Biochem.
, vol.113
, pp. 313-317
-
-
Heinonen, J.K.1
Lahti, R.J.2
-
37
-
-
0023283932
-
2+-sensitivity of the ATPase activity of rabbit skeletal myofibrils: Effect of the complete substitution of troponin C with cardiac troponin C, calmodulin, and parvalbumins
-
2+-sensitivity of the ATPase activity of rabbit skeletal myofibrils: effect of the complete substitution of troponin C with cardiac troponin C, calmodulin, and parvalbumins J. Biochem. 101, 291-301
-
(1987)
J. Biochem.
, vol.101
, pp. 291-301
-
-
Morimoto, S.1
Ohtsuki, I.2
-
38
-
-
0014949207
-
Cleavage of structural proteins during the assembly of the head of bacteriophage T4
-
Laemmli, U.K. (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227, 680-685
-
(1970)
Nature
, vol.227
, pp. 680-685
-
-
Laemmli, U.K.1
-
39
-
-
0033214054
-
Functional consequences of troponin T mutations found in hypertrophic cardiomyopathy
-
Tobacman, L.S., Lin, D., Butters, C., Landis, C., Back, N., Pavlov, D., and Homsher, E. (1999) Functional consequences of troponin T mutations found in hypertrophic cardiomyopathy. J. Biol. Chem. 274, 28363-28370
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 28363-28370
-
-
Tobacman, L.S.1
Lin, D.2
Butters, C.3
Landis, C.4
Back, N.5
Pavlov, D.6
Homsher, E.7
-
40
-
-
0032483037
-
Patients with familial hypertrophic cardiomyopathy caused by a Phe110Ile missense mutation in the cardiac troponin T gene have variable cardiac morphologies and a favorable prognosis
-
Anan, R., Shono, H., Kisanuki, A., Arima, S., Nakao, S., and Tanaka, H. (1998) Patients with familial hypertrophic cardiomyopathy caused by a Phe110Ile missense mutation in the cardiac troponin T gene have variable cardiac morphologies and a favorable prognosis. Circulation 98, 391-397
-
(1998)
Circulation
, vol.98
, pp. 391-397
-
-
Anan, R.1
Shono, H.2
Kisanuki, A.3
Arima, S.4
Nakao, S.5
Tanaka, H.6
|