-
1
-
-
0030922569
-
Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy
-
Ortiz-Lopez, R., Li, H., Su, J., Goytia, V. and Towbin, J.A. (1997) Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy. Circulation, 5, 2434-2440.
-
(1997)
Circulation
, vol.5
, pp. 2434-2440
-
-
Ortiz-Lopez, R.1
Li, H.2
Su, J.3
Goytia, V.4
Towbin, J.A.5
-
2
-
-
0037192309
-
Metavinculin mutations alter actin interaction in dilated cardiomyopathy
-
Olson, T.M., Illenberger, S., Kishimoto, N.Y., Huttelmaier, S., Keating, M.T. and Jockusch, B.M. (2002) Metavinculin mutations alter actin interaction in dilated cardiomyopathy. Circulation, 105, 431-437.
-
(2002)
Circulation
, vol.105
, pp. 431-437
-
-
Olson, T.M.1
Illenberger, S.2
Kishimoto, N.Y.3
Huttelmaier, S.4
Keating, M.T.5
Jockusch, B.M.6
-
3
-
-
0033520037
-
Desmin mutation responsible for idiopathic dilated cardiomyopathy
-
Li, D., Tapscoft, T., Gonzalez, O., Burch, P.E., Quiñones, M.A., Zoghbi, W.A., Hill, R., Bachinski, L.L., Mann, D.L. and Roberts, R. (1999) Desmin mutation responsible for idiopathic dilated cardiomyopathy. Circulation, 100, 461-464.
-
(1999)
Circulation
, vol.100
, pp. 461-464
-
-
Li, D.1
Tapscoft, T.2
Gonzalez, O.3
Burch, P.E.4
Quiñones, M.A.5
Zoghbi, W.A.6
Hill, R.7
Bachinski, L.L.8
Mann, D.L.9
Roberts, R.10
-
4
-
-
0036478897
-
Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy
-
Gerull, B., Gramlich, M., Atherton, J., McNabb, M., Trombitás, K., Sasse-Klaassen, S., Seidman, J.G., Seidman, C., Granzier, H., Labeit, S. et al. (2002) Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy. Nat. Genet., 30 201-204.
-
(2002)
Nat. Genet
, vol.30
, pp. 201-204
-
-
Gerull, B.1
Gramlich, M.2
Atherton, J.3
McNabb, M.4
Trombitás, K.5
Sasse-Klaassen, S.6
Seidman, J.G.7
Seidman, C.8
Granzier, H.9
Labeit, S.10
-
5
-
-
0032076955
-
Actin mutations in dilated cardiomyopathy, a heritable form of heart failure
-
Olson, T.M., Michels, V.V., Thibodeau, S.N., Tai, Y.S. and Keating, M.T. (1998) Actin mutations in dilated cardiomyopathy, a heritable form of heart failure. Science, 280, 750-752.
-
(1998)
Science
, vol.280
, pp. 750-752
-
-
Olson, T.M.1
Michels, V.V.2
Thibodeau, S.N.3
Tai, Y.S.4
Keating, M.T.5
-
6
-
-
17444407002
-
Mutation screening in dilated cardiomyopathy: Prominent role of the beta myosin heavy chain gene
-
Villard, E., Duboscq-Bidot, L., Charron, P., Benaiche, A., Conraads, V., Sylvius, N. and Komajda, M. (2005) Mutation screening in dilated cardiomyopathy: Prominent role of the beta myosin heavy chain gene. Eur. Heart J., 26, 794-803.
-
(2005)
Eur. Heart J
, vol.26
, pp. 794-803
-
-
Villard, E.1
Duboscq-Bidot, L.2
Charron, P.3
Benaiche, A.4
Conraads, V.5
Sylvius, N.6
Komajda, M.7
-
7
-
-
0037154179
-
Ca(2+)-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathy
-
Morimoto, S., Lu, Q.W., Harada, K., Takahashi-Yanaga, F., Minakami, R., Ohta, M., Sasaguri, T. and Ohtsuki, I. (2002) Ca(2+)-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathy. Proc. Natl Acad. Sci. USA, 99, 913-918.
-
(2002)
Proc. Natl Acad. Sci. USA
, vol.99
, pp. 913-918
-
-
Morimoto, S.1
Lu, Q.W.2
Harada, K.3
Takahashi-Yanaga, F.4
Minakami, R.5
Ohta, M.6
Sasaguri, T.7
Ohtsuki, I.8
-
8
-
-
0037184992
-
The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy
-
Knöll, R., Hoshijima, M., Hoffman, H.M., Person, V., Lorenzen-Schmidt, I., Bang, M.L., Hayashi, T., Shiga, N., Yasukawa, H., Schaper, W. et al. (2002) The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy. Cell, 111, 943-955.
-
(2002)
Cell
, vol.111
, pp. 943-955
-
-
Knöll, R.1
Hoshijima, M.2
Hoffman, H.M.3
Person, V.4
Lorenzen-Schmidt, I.5
Bang, M.L.6
Hayashi, T.7
Shiga, N.8
Yasukawa, H.9
Schaper, W.10
-
9
-
-
0034619996
-
Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy
-
Kamisago, M., Sharma, S.D., DePalma, S.R., Solomon, S., Sharma, P., McDonough, B., Smoot, L., Mullen, M.P., Woolf, P.K., Wigle, E.D. et al. (2000) Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy. N. Engl. J. Med., 343, 1688-1696.
-
(2000)
N. Engl. J. Med
, vol.343
, pp. 1688-1696
-
-
Kamisago, M.1
Sharma, S.D.2
DePalma, S.R.3
Solomon, S.4
Sharma, P.5
McDonough, B.6
Smoot, L.7
Mullen, M.P.8
Woolf, P.K.9
Wigle, E.D.10
-
10
-
-
0037174918
-
Alterations in thin filament regulation induced by a human cardiac troponin T mutant that causes dilated cardiomyopathy are distinct from those induced by troponin T mutants that cause hypertrophic cardiomyopathy
-
Robinson, P., Mirza, M., Knott, A., Abdulrazzak, H., Willott, R., Marston, S., Watkins, H. and Redwood, C. (2002) Alterations in thin filament regulation induced by a human cardiac troponin T mutant that causes dilated cardiomyopathy are distinct from those induced by troponin T mutants that cause hypertrophic cardiomyopathy. J. Biol. Chem., 277, 40710-40716.
-
(2002)
J. Biol. Chem
, vol.277
, pp. 40710-40716
-
-
Robinson, P.1
Mirza, M.2
Knott, A.3
Abdulrazzak, H.4
Willott, R.5
Marston, S.6
Watkins, H.7
Redwood, C.8
-
11
-
-
0032701644
-
Complexity in simplicity: Monogenic disorders and complex cardiomyopathies
-
Chen, J. and Chien, K.R. (1999) Complexity in simplicity: Monogenic disorders and complex cardiomyopathies. J. Clin. Invest., 103 1483-1485.
-
(1999)
J. Clin. Invest
, vol.103
, pp. 1483-1485
-
-
Chen, J.1
Chien, K.R.2
-
12
-
-
0035936792
-
The genetic basis for cardiomyopathy: From mutation identification to mechanistic paradigms
-
Seidman, J.G. and Seidman, C. (2001) The genetic basis for cardiomyopathy: From mutation identification to mechanistic paradigms. Cell, 104, 557-567.
-
(2001)
Cell
, vol.104
, pp. 557-567
-
-
Seidman, J.G.1
Seidman, C.2
-
13
-
-
33746038182
-
Dilated cardiomyopathy: A tale of cytoskeletal proteins and beyond
-
Towbin, J.A. and Bowles, N.E. (2006) Dilated cardiomyopathy: A tale of cytoskeletal proteins and beyond. J. Cardiovasc. Electrophysiol., 17, 919-926.
-
(2006)
J. Cardiovasc. Electrophysiol
, vol.17
, pp. 919-926
-
-
Towbin, J.A.1
Bowles, N.E.2
-
14
-
-
2342621479
-
The dystrophin glycoprotein complex: Signaling strength and integrity for the sarcolemma
-
Lapidos, K.A., Kakkar, R. and McNally, E.M. (2004) The dystrophin glycoprotein complex: Signaling strength and integrity for the sarcolemma. Circ. Res., 94, 1023-1031.
-
(2004)
Circ. Res
, vol.94
, pp. 1023-1031
-
-
Lapidos, K.A.1
Kakkar, R.2
McNally, E.M.3
-
15
-
-
44649142005
-
Sarcomere mutations in cardiomyopathy, noncompaction, and the developing heart
-
Dellefave, L. and McNally, E.M. (2008) Sarcomere mutations in cardiomyopathy, noncompaction, and the developing heart. Circulation 117, 2847-2849.
-
(2008)
Circulation
, vol.117
, pp. 2847-2849
-
-
Dellefave, L.1
McNally, E.M.2
-
16
-
-
0033538565
-
-
Zhou, Q., Ruiz-Lozano, P., Martone, M.E. and Chen, J. (1999) Cypher, a striated muscle-restricted PDZ and LIM domain-containing protein, binds to alpha-actinin-2 and protein kinase C. J. Biol. Chem., 274 19807-19813.
-
Zhou, Q., Ruiz-Lozano, P., Martone, M.E. and Chen, J. (1999) Cypher, a striated muscle-restricted PDZ and LIM domain-containing protein, binds to alpha-actinin-2 and protein kinase C. J. Biol. Chem., 274 19807-19813.
-
-
-
-
17
-
-
84924110084
-
Ablation of Cypher, a PDZ-LIM domain Z-line protein, causes a severe form of congenital myopathy
-
Zhou, Q., Chu, P.H., Huang, C., Cheng, C.F., Martone, M.E., Knoll, G., Shelton, G.D., Evans, S. and Chen, J. (2001) Ablation of Cypher, a PDZ-LIM domain Z-line protein, causes a severe form of congenital myopathy. J. Cell. Biol., 155, 605-612.
-
(2001)
J. Cell. Biol
, vol.155
, pp. 605-612
-
-
Zhou, Q.1
Chu, P.H.2
Huang, C.3
Cheng, C.F.4
Martone, M.E.5
Knoll, G.6
Shelton, G.D.7
Evans, S.8
Chen, J.9
-
18
-
-
0344873698
-
Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction
-
Vatta, M., Mohapatra, B., Jimenez, S., Sanchez, X., Faulkner, G., Perles, Z., Sinagra, G., Lin, J.H., Vu, T.M., Zhou, Q. et al. (2003) Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction. J. Am. Coll. Cardiol., 42 2014-2027.
-
(2003)
J. Am. Coll. Cardiol
, vol.42
, pp. 2014-2027
-
-
Vatta, M.1
Mohapatra, B.2
Jimenez, S.3
Sanchez, X.4
Faulkner, G.5
Perles, Z.6
Sinagra, G.7
Lin, J.H.8
Vu, T.M.9
Zhou, Q.10
-
19
-
-
33646058879
-
Genetic analysis in patients with left ventricular noncompaction and evidence for genetic heterogeneity
-
Xing, Y., Ichida, F., Matsuoka, T., Isobe, T., Ikemoto, Y., Higaki, T., Tsuji, T., Haneda, N., Kuwabara, A., Chen, R. et al. (2006) Genetic analysis in patients with left ventricular noncompaction and evidence for genetic heterogeneity. Mol. Genet. Metab., 88, 71-77.
-
(2006)
Mol. Genet. Metab
, vol.88
, pp. 71-77
-
-
Xing, Y.1
Ichida, F.2
Matsuoka, T.3
Isobe, T.4
Ikemoto, Y.5
Higaki, T.6
Tsuji, T.7
Haneda, N.8
Kuwabara, A.9
Chen, R.10
-
20
-
-
10744231114
-
-
Arimura, T., Hayashi, T., Terada, H., Lee, S.Y., Zhou, Q., Takahashi, M., Ueda, K., Nouchi, T., Hohda, S., Shibutani, M. et al. (2004) A Cypher/ZASP mutation associated with dilated cardiomyopathy alters the binding affinity to protein kinase C. J. Biol. Chem., 279, 6746-6752.
-
Arimura, T., Hayashi, T., Terada, H., Lee, S.Y., Zhou, Q., Takahashi, M., Ueda, K., Nouchi, T., Hohda, S., Shibutani, M. et al. (2004) A Cypher/ZASP mutation associated with dilated cardiomyopathy alters the binding affinity to protein kinase C. J. Biol. Chem., 279, 6746-6752.
-
-
-
-
21
-
-
33750816260
-
Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathy
-
Theis, J.L., Bos, J.M., Bartleson, V.B., Will, M.L., Binder, J., Vatta, M., Towbin, J.A., Gersh, B.J., Ommen, S.R. and Ackerman, M.J. (2006) Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathy. Biochem. Biophys. Res. Commun., 351, 896-902.
-
(2006)
Biochem. Biophys. Res. Commun
, vol.351
, pp. 896-902
-
-
Theis, J.L.1
Bos, J.M.2
Bartleson, V.B.3
Will, M.L.4
Binder, J.5
Vatta, M.6
Towbin, J.A.7
Gersh, B.J.8
Ommen, S.R.9
Ackerman, M.J.10
-
22
-
-
36049003590
-
Z'eroing in on the role of Cypher in striated muscle function, signaling, and human disease
-
Sheikh, F., Bang, M.L., Lange, S. and Chen, J. (2007) 'Z'eroing in on the role of Cypher in striated muscle function, signaling, and human disease. Trends Cardiovasc. Med., 17, 258-262.
-
(2007)
Trends Cardiovasc. Med
, vol.17
, pp. 258-262
-
-
Sheikh, F.1
Bang, M.L.2
Lange, S.3
Chen, J.4
-
23
-
-
13144260646
-
Mutations in ZASP define a novel form of muscular dystrophy in humans
-
Selcen, D. and Engel, A.G. (2005) Mutations in ZASP define a novel form of muscular dystrophy in humans. Ann. Neurol., 57, 269-276.
-
(2005)
Ann. Neurol
, vol.57
, pp. 269-276
-
-
Selcen, D.1
Engel, A.G.2
-
24
-
-
0031984869
-
Selective requirement of myosin light chain 2v in embryonic heart function
-
Chen, J., Kubalak, S.W., Minamisawa, S., Price, R.L., Becker, K.D., Hickey, R., Ross, J.J. and Chien, K.R. (1998) Selective requirement of myosin light chain 2v in embryonic heart function. J. Biol. Chem., 273, 1252-1256.
-
(1998)
J. Biol. Chem
, vol.273
, pp. 1252-1256
-
-
Chen, J.1
Kubalak, S.W.2
Minamisawa, S.3
Price, R.L.4
Becker, K.D.5
Hickey, R.6
Ross, J.J.7
Chien, K.R.8
-
25
-
-
0035816733
-
Temporally regulated and tissue-specific gene manipulations in the adult and embryonic heart using a tamoxifen-inducible Cre protein
-
Sohal, D.S., Nghiem, M., Crackower, M.A., Witt, S.A., Kimball, T.R., Tymitz, K.M., Penninger, J.M. and Molkentin, J.D. (2001) Temporally regulated and tissue-specific gene manipulations in the adult and embryonic heart using a tamoxifen-inducible Cre protein. Circ. Res. 89, 20-25.
-
(2001)
Circ. Res
, vol.89
, pp. 20-25
-
-
Sohal, D.S.1
Nghiem, M.2
Crackower, M.A.3
Witt, S.A.4
Kimball, T.R.5
Tymitz, K.M.6
Penninger, J.M.7
Molkentin, J.D.8
-
26
-
-
0037470052
-
Characterization and in vivo functional analysis of splice variants of Cypher
-
Huang, C., Zhou, Q., Liang, P., Hollander, M.S., Sheikh, F., Li, X., Greaser, M., Shelton, G.D., Evans, S. and Chen, J. (2003) Characterization and in vivo functional analysis of splice variants of Cypher. J. Biol. Chem., 278, 7360-7365.
-
(2003)
J. Biol. Chem
, vol.278
, pp. 7360-7365
-
-
Huang, C.1
Zhou, Q.2
Liang, P.3
Hollander, M.S.4
Sheikh, F.5
Li, X.6
Greaser, M.7
Shelton, G.D.8
Evans, S.9
Chen, J.10
-
27
-
-
0037134462
-
Calsarcin-3, a novel skeletal muscle-specific member of the calsarcin family, interacts with multiple Z-disc proteins
-
Frey, N. and Olson, E.N. (2002) Calsarcin-3, a novel skeletal muscle-specific member of the calsarcin family, interacts with multiple Z-disc proteins. J. Biol. Chem., 277, 13998-14004.
-
(2002)
J. Biol. Chem
, vol.277
, pp. 13998-14004
-
-
Frey, N.1
Olson, E.N.2
-
28
-
-
0012927828
-
PDZ domain proteins: Plug and play
-
Nourry, C., Grant, S.G. and Borg, J.P. (2003) PDZ domain proteins: Plug and play. Sci. STKE, 179, RE7.
-
(2003)
Sci. STKE
, vol.179
-
-
Nourry, C.1
Grant, S.G.2
Borg, J.P.3
-
29
-
-
0344759163
-
Myotilin, a novel sarcomeric protein with two Ig-like domains, is encoded by a candidate gene for limb-girdle muscular dystrophy
-
Salmikangas, P., Mykkänen, O.M., Grönholm, M., Heiska, L., Kere, J. and Carpén, O. (1999) Myotilin, a novel sarcomeric protein with two Ig-like domains, is encoded by a candidate gene for limb-girdle muscular dystrophy. Hum. Mol. Genet., 8, 1329-1336.
-
(1999)
Hum. Mol. Genet
, vol.8
, pp. 1329-1336
-
-
Salmikangas, P.1
Mykkänen, O.M.2
Grönholm, M.3
Heiska, L.4
Kere, J.5
Carpén, O.6
-
30
-
-
24944550989
-
The Z-disc proteins myotilin and FATZ-1 interact with each other and are connected to the sarcolemma via muscle-specific filamins
-
Gontier, Y., Taivainen, A., Fontao, L., Sonnenberg, A., van der Flier, A., Carpen, O., Faulkner, G. and Borradori, L. (2005) The Z-disc proteins myotilin and FATZ-1 interact with each other and are connected to the sarcolemma via muscle-specific filamins. J. Cell. Sci., 118, 3739-3749.
-
(2005)
J. Cell. Sci
, vol.118
, pp. 3739-3749
-
-
Gontier, Y.1
Taivainen, A.2
Fontao, L.3
Sonnenberg, A.4
van der Flier, A.5
Carpen, O.6
Faulkner, G.7
Borradori, L.8
-
31
-
-
0034675887
-
Indications for a novel muscular dystrophy pathway: Gamma-filamin, the muscle-specific filamin isoform, interacts with myotilin
-
van der Ven, P.F., Wiesner, S., Salmikangas, P., Auerbach, D., Himmel, M., Kempa, S., Hayess, K., Pacholsky, D., Taivainen, A., Schröder, R. et al. (2000) Indications for a novel muscular dystrophy pathway: gamma-filamin, the muscle-specific filamin isoform, interacts with myotilin. J. Cell. Biol., 151, 235-248.
-
(2000)
J. Cell. Biol
, vol.151
, pp. 235-248
-
-
van der Ven, P.F.1
Wiesner, S.2
Salmikangas, P.3
Auerbach, D.4
Himmel, M.5
Kempa, S.6
Hayess, K.7
Pacholsky, D.8
Taivainen, A.9
Schröder, R.10
-
32
-
-
0033606789
-
ZASP: A new Z-band alternatively spliced PDZ-motif protein
-
Faulkner, G., Pallavicini, A., Formentin, E., Comelli, A., Ievolella, C., Trevisan, S., Bortoletto, G., Scannapieco, P., Salamon, M., Mouly, V. et al. (1999) ZASP: A new Z-band alternatively spliced PDZ-motif protein. J. Cell. Biol., 146, 465-475.
-
(1999)
J. Cell. Biol
, vol.146
, pp. 465-475
-
-
Faulkner, G.1
Pallavicini, A.2
Formentin, E.3
Comelli, A.4
Ievolella, C.5
Trevisan, S.6
Bortoletto, G.7
Scannapieco, P.8
Salamon, M.9
Mouly, V.10
-
33
-
-
0034284682
-
Myotilin is mutated in limb girdle muscular dystrophy 1A
-
Hauser, M.A., Horrigan, S.K., Salmikangas, P., Torian, U.M., Viles, K.D., Dancel, R., Tim, R.W., Taivainen, A., Bartoloni, L., Gilchrist, J.M. et al. (2000) Myotilin is mutated in limb girdle muscular dystrophy 1A. Hum. Mol. Genet., 9, 2141-2147.
-
(2000)
Hum. Mol. Genet
, vol.9
, pp. 2141-2147
-
-
Hauser, M.A.1
Horrigan, S.K.2
Salmikangas, P.3
Torian, U.M.4
Viles, K.D.5
Dancel, R.6
Tim, R.W.7
Taivainen, A.8
Bartoloni, L.9
Gilchrist, J.M.10
-
34
-
-
1942473823
-
Mutations in myotilin cause myofibrillar myopathy
-
Selcen, D. and Engel, A.G. (2004) Mutations in myotilin cause myofibrillar myopathy. Neurology, 62, 1363-1371.
-
(2004)
Neurology
, vol.62
, pp. 1363-1371
-
-
Selcen, D.1
Engel, A.G.2
-
35
-
-
33748360319
-
Identification of 45 novel mutations in the nebulin gene associated with autosomal recessive nemaline myopathy
-
Lehtokari, V.L., Pelin, K., Sandbacka, M., Ranta, S., Donner, K., Muntoni, F., Sewry, C., Angelini, C., Bushby, K., Van den Bergh, P. et al. (2006) Identification of 45 novel mutations in the nebulin gene associated with autosomal recessive nemaline myopathy. Hum. Mutat., 27, 946-956.
-
(2006)
Hum. Mutat
, vol.27
, pp. 946-956
-
-
Lehtokari, V.L.1
Pelin, K.2
Sandbacka, M.3
Ranta, S.4
Donner, K.5
Muntoni, F.6
Sewry, C.7
Angelini, C.8
Bushby, K.9
Van den Bergh, P.10
-
36
-
-
30944435503
-
Sarcomeric protein mutations in dilated cardiomyopathy
-
Chang, A.N. and Potter, J.D. (2005) Sarcomeric protein mutations in dilated cardiomyopathy. Heart Fail Rev., 10, 225-235.
-
(2005)
Heart Fail Rev
, vol.10
, pp. 225-235
-
-
Chang, A.N.1
Potter, J.D.2
-
37
-
-
53749089626
-
The dynamic Z bands of striated muscle cells
-
Sanger, J.M. and Sanger, J.W. (2008) The dynamic Z bands of striated muscle cells. Sci. Signal., 1, e37.
-
(2008)
Sci. Signal
, vol.1
-
-
Sanger, J.M.1
Sanger, J.W.2
-
38
-
-
33845801599
-
Targeted deletion of the muscular dystrophy gene myotilin does not perturb muscle structure or function in mice
-
Moza, M., Mologni, L., Trokovic, R., Faulkner, G., Partanen, J. and Carpén, O. (2007) Targeted deletion of the muscular dystrophy gene myotilin does not perturb muscle structure or function in mice. Mol. Cell. Biol., 27, 244-252.
-
(2007)
Mol. Cell. Biol
, vol.27
, pp. 244-252
-
-
Moza, M.1
Mologni, L.2
Trokovic, R.3
Faulkner, G.4
Partanen, J.5
Carpén, O.6
-
39
-
-
19944423058
-
Mice lacking calsarcin-1 are sensitized to calcineurin signaling and show accelerated cardiomyopathy in response to pathological biomechanical stress
-
Frey, N., Barrientos, T., Shelton, J.M., Frank, D., Rütten, H., Gehring, D., Kuhn, C., Lutz, M., Rothermel, B., Bassel-Duby, R. et al. (2004) Mice lacking calsarcin-1 are sensitized to calcineurin signaling and show accelerated cardiomyopathy in response to pathological biomechanical stress. Nat. Med., 10, 1336-1343.
-
(2004)
Nat. Med
, vol.10
, pp. 1336-1343
-
-
Frey, N.1
Barrientos, T.2
Shelton, J.M.3
Frank, D.4
Rütten, H.5
Gehring, D.6
Kuhn, C.7
Lutz, M.8
Rothermel, B.9
Bassel-Duby, R.10
-
40
-
-
0038182574
-
Dystrophin-glycoprotein complex: Post-translational processing and dystroglycan function
-
Michele, D.E. and Campbell, K.P. (2003) Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function. J. Biol. Chem., 278, 15457-15460.
-
(2003)
J. Biol. Chem
, vol.278
, pp. 15457-15460
-
-
Michele, D.E.1
Campbell, K.P.2
-
41
-
-
55249123610
-
Multiplex kinase signaling modifies cardiac function at the level of sarcomeric proteins
-
Solaro, R.J. (2008) Multiplex kinase signaling modifies cardiac function at the level of sarcomeric proteins. J. Biol. Chem, 283, 26829-26833.
-
(2008)
J. Biol. Chem
, vol.283
, pp. 26829-26833
-
-
Solaro, R.J.1
-
42
-
-
0038757610
-
Mitogen-activated protein kinases: A new therapeutic target in cardiac pathology
-
Ravingerová, T., Barancík, M. and Strnisková, M. (2003) Mitogen-activated protein kinases: A new therapeutic target in cardiac pathology. Mol. Cell. Biochem., 247, 127-138.
-
(2003)
Mol. Cell. Biochem
, vol.247
, pp. 127-138
-
-
Ravingerová, T.1
Barancík, M.2
Strnisková, M.3
-
43
-
-
40849101607
-
A role for p38alpha mitogen-activated protein kinase in embryonic cardiac differentiation
-
Hernández-Torres, F., Martínez-Fernández, S., Zuluaga, S., Nebreda, A., Porras, A., Aránega, A.E. and Navarro, F. (2008) A role for p38alpha mitogen-activated protein kinase in embryonic cardiac differentiation. FEBS Lett., 582, 1025-1031.
-
(2008)
FEBS Lett
, vol.582
, pp. 1025-1031
-
-
Hernández-Torres, F.1
Martínez-Fernández, S.2
Zuluaga, S.3
Nebreda, A.4
Porras, A.5
Aránega, A.E.6
Navarro, F.7
-
44
-
-
33746325064
-
p38 mitogen-activated protein kinase activity commits embryonic stem cells to either neurogenesis or cardiomyogenesis
-
Aouadi, M., Bost, F., Caron, L., Laurent, K., Le Marchand Brustel, Y. and Binétruy, B. (2006) p38 mitogen-activated protein kinase activity commits embryonic stem cells to either neurogenesis or cardiomyogenesis. Stem Cells, 24, 1399-1406.
-
(2006)
Stem Cells
, vol.24
, pp. 1399-1406
-
-
Aouadi, M.1
Bost, F.2
Caron, L.3
Laurent, K.4
Le Marchand Brustel, Y.5
Binétruy, B.6
-
45
-
-
1542613386
-
Stress-activated MAP kinases in cardiac remodeling and heart failure; new insights from transgenic studies
-
Petrich, B.G. and Wang, Y. (2004) Stress-activated MAP kinases in cardiac remodeling and heart failure; new insights from transgenic studies. Trends Cardiovasc. Med., 14, 50-55.
-
(2004)
Trends Cardiovasc. Med
, vol.14
, pp. 50-55
-
-
Petrich, B.G.1
Wang, Y.2
-
46
-
-
0037448803
-
Alterations in Janus kinase (JAK)-signal transducers and activators of transcription (STAT) signaling in patients with end-stage dilated cardiomyopathy
-
Podewski, E.K., Hilfiker-Kleiner, D., Hilfiker, A., Morawietz, H., Lichtenberg, A., Wollert, K.C. and Drexler, H. (2003) Alterations in Janus kinase (JAK)-signal transducers and activators of transcription (STAT) signaling in patients with end-stage dilated cardiomyopathy. Circulation, 107, 798-802.
-
(2003)
Circulation
, vol.107
, pp. 798-802
-
-
Podewski, E.K.1
Hilfiker-Kleiner, D.2
Hilfiker, A.3
Morawietz, H.4
Lichtenberg, A.5
Wollert, K.C.6
Drexler, H.7
-
47
-
-
0034602781
-
Signal transductor and activator of transcription 3 in the heart transduces not only a hypertrophic signal but a protective signal against doxorubicin induced cardiomyopathy
-
Kunisada, K., Negoro, S., Tone, E., Funamoto, M., Osugi, T., Yamada, S., Okabe, M., Kishimoto, T. and Yamauchi-Takihara, K. (2000) Signal transductor and activator of transcription 3 in the heart transduces not only a hypertrophic signal but a protective signal against doxorubicin induced cardiomyopathy. Proc. Natl Acad. Sci. USA, 97, 315-319.
-
(2000)
Proc. Natl Acad. Sci. USA
, vol.97
, pp. 315-319
-
-
Kunisada, K.1
Negoro, S.2
Tone, E.3
Funamoto, M.4
Osugi, T.5
Yamada, S.6
Okabe, M.7
Kishimoto, T.8
Yamauchi-Takihara, K.9
-
48
-
-
0242268405
-
Cardiomyocyte-restricted knockout of STAT3 results in higher sensitivity to inflammation, cardiac fibrosis, and heart failure with advanced age
-
Jacoby, J.J., Kalinowski, A., Liu, M.G., Zhang, S.S., Gao, Q., Chai, G.X., Ji, L., Iwamoto, Y., Li, E., Schneider, M. et al. (2003) Cardiomyocyte-restricted knockout of STAT3 results in higher sensitivity to inflammation, cardiac fibrosis, and heart failure with advanced age. Proc. Natl Acad. Sci. USA, 100, 12929-12934.
-
(2003)
Proc. Natl Acad. Sci. USA
, vol.100
, pp. 12929-12934
-
-
Jacoby, J.J.1
Kalinowski, A.2
Liu, M.G.3
Zhang, S.S.4
Gao, Q.5
Chai, G.X.6
Ji, L.7
Iwamoto, Y.8
Li, E.9
Schneider, M.10
-
49
-
-
41949129330
-
Severe heart failure and early mortality in a double-mutation mouse model of familial hypertrophic cardiomyopathy
-
Tsoutsman, T., Kelly, M., Ng, D.C., Tan, J.E., Tu, E., Lam, L., Bogoyevitch, M.A., Seidman, C.E., Seidman, J.G. and Semsarian, C. (2008) Severe heart failure and early mortality in a double-mutation mouse model of familial hypertrophic cardiomyopathy. Circulation, 117 1820-1831.
-
(2008)
Circulation
, vol.117
, pp. 1820-1831
-
-
Tsoutsman, T.1
Kelly, M.2
Ng, D.C.3
Tan, J.E.4
Tu, E.5
Lam, L.6
Bogoyevitch, M.A.7
Seidman, C.E.8
Seidman, J.G.9
Semsarian, C.10
-
50
-
-
21844436786
-
Endothelin-1-induced arrhythmogenic Ca2+ signaling is abolished in atrial myocytes of inositol-1,4,5-trisphosphate(IP3)-receptor type 2-deficient mice
-
Li, X., Zima, A.V., Sheikh, F., Blatter, L.A. and Chen, J. (2005) Endothelin-1-induced arrhythmogenic Ca2+ signaling is abolished in atrial myocytes of inositol-1,4,5-trisphosphate(IP3)-receptor type 2-deficient mice. Circ. Res., 96, 1274-1281.
-
(2005)
Circ. Res
, vol.96
, pp. 1274-1281
-
-
Li, X.1
Zima, A.V.2
Sheikh, F.3
Blatter, L.A.4
Chen, J.5
-
51
-
-
11244305854
-
Intracellular acidosis-activated p38 MAPK signaling and its essential role in cardiomyocyte hypoxic injury
-
Zheng, M., Reynolds, C., Jo, S.H., Wersto, R., Han, Q. and Xiao, R.P. (2005) Intracellular acidosis-activated p38 MAPK signaling and its essential role in cardiomyocyte hypoxic injury. FASEB J., 19 109-111.
-
(2005)
FASEB J
, vol.19
, pp. 109-111
-
-
Zheng, M.1
Reynolds, C.2
Jo, S.H.3
Wersto, R.4
Han, Q.5
Xiao, R.P.6
-
52
-
-
10244221064
-
Ablation of the murine alpha myosin heavy chain gene leads to dosage effects and functional deficits in the heart
-
Jones, W.K., Grupp, I.L., Doetschman, T., Grupp, G., Osinska, H., Hewett, T.E., Boivin, G., Gulick, J., Ng, W.A. and Robbins, J. (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
-
53
-
-
0029788179
-
Transthoracic echocardiography in models of cardiac disease in the mouse
-
Tanaka, N., Dalton, N., Mao, L., Rockman, H.A., Peterson, K.L., Gottshall, K.R., Hunter, J.J., Chien, K.R. and Ross, J., Jr (1996) Transthoracic echocardiography in models of cardiac disease in the mouse. Circulation, 94, 1109-1117.
-
(1996)
Circulation
, vol.94
, pp. 1109-1117
-
-
Tanaka, N.1
Dalton, N.2
Mao, L.3
Rockman, H.A.4
Peterson, K.L.5
Gottshall, K.R.6
Hunter, J.J.7
Chien, K.R.8
Ross Jr, J.9
|