-
1
-
-
0030933063
-
MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure
-
Arber, S., Hunter, J.J., Ross, J., Jr., Hongo, M., Sansig, G., Borg, J., Perriard, J.C., Chien, K.R., and Caroni, P. (1997). MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure. Cell 88, 393-403.
-
(1997)
Cell
, vol.88
, pp. 393-403
-
-
Arber, S.1
Hunter, J.J.2
Ross Jr., J.3
Hongo, M.4
Sansig, G.5
Borg, J.6
Perriard, J.C.7
Chien, K.R.8
Caroni, P.9
-
2
-
-
0033017374
-
Enteroviral protease 2 Àcleaves dystrophin: Evidence of cytoskeletal disruption in an acquired cardiomyopathy
-
Badorff, C., Lee G.H., Lamphear, B.J., Maitone, M.E., Campbell, K.P., Rhoads, R.E., and Knowlton, K.U. (1999). Enteroviral protease 2 Àcleaves dystrophin: evidence of cytoskeletal disruption in an acquired cardiomyopathy. Nat. Med. 5, 320-326.
-
(1999)
Nat. Med.
, vol.5
, pp. 320-326
-
-
Badorff, C.1
Lee, G.H.2
Lamphear, B.J.3
Maitone, M.E.4
Campbell, K.P.5
Rhoads, R.E.6
Knowlton, K.U.7
-
3
-
-
0032977685
-
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
-
Bonne, G., Di Barletta, M.R., Varnous, S., Becane, H.M., Hammouda, E.H., Merlini, l., Muntoni, F., Greenberg, C.R., Gary, F., Urtizberea, U.A., et al. (1999). Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy. Nat. Genet. 21, 285-288.
-
(1999)
Nat. Genet.
, vol.21
, pp. 285-288
-
-
Bonne, G.1
Di Barletta, M.R.2
Varnous, S.3
Becane, H.M.4
Hammouda, E.H.5
Merlini, L.6
Muntoni, F.7
Greenberg, C.R.8
Gary, F.9
Urtizberea, U.A.10
-
4
-
-
0031451562
-
Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex
-
Crosbie, R.H., Heighway, J., Venzke, D.P., Lee, U.C., and Campbell, K.P. (1997). Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex. J. Biol. Chem. 272, 31221-31224.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 31221-31224
-
-
Crosbie, R.H.1
Heighway, J.2
Venzke, D.P.3
Lee, U.C.4
Campbell, K.P.5
-
5
-
-
0033526085
-
Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex
-
Crosbie, R.H., Lebakken, O.S., Holt, K.H., Venzke, O.P., Sträub, V., Lee, U.C., Grady, R.M., Chamberlain, U.S., Sanes, U.R., and Campbell, K.P (1999). Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex. J. Cell Biol. 145, 153-165.
-
(1999)
J. Cell Biol.
, vol.145
, pp. 153-165
-
-
Crosbie, R.H.1
Lebakken, O.S.2
Holt, K.H.3
Venzke, O.P.4
Sträub, V.5
Lee, U.C.6
Grady, R.M.7
Chamberlain, U.S.8
Sanes, U.R.9
Campbell, K.P.10
-
6
-
-
19244372467
-
Progressive muscular dystrophy in alphasarcoglycan-deficient mice
-
Duclos, F., Straub, V., Moore, S.A., Venzke, D.P., Hrstka, R.F., Crosbie, R.H., Durbeej, M., Lebakken, C.S., Ettinger A.J., and van der Meulen, J., et al. (1998). Progressive muscular dystrophy in alphasarcoglycan-deficient mice. J. Cell Biol. 742, 1461-1471.
-
(1998)
J. Cell Biol.
, vol.742
, pp. 1461-1471
-
-
Duclos, F.1
Straub, V.2
Moore, S.A.3
Venzke, D.P.4
Hrstka, R.F.5
Crosbie, R.H.6
Durbeej, M.7
Lebakken, C.S.8
Ettinger, A.J.9
Van Der Meulen, J.10
-
7
-
-
0027275643
-
A role for the dystrophinglycoprotein complex as a transmembrane linker between laminin and actin
-
Ervasti, J.M., and Campbell, K.P. (1993). A role for the dystrophinglycoprotein complex as a transmembrane linker between laminin and actin. J. Cell Biol. 122, 809-823.
-
(1993)
J. Cell Biol.
, vol.122
, pp. 809-823
-
-
Ervasti, J.M.1
Campbell, K.P.2
-
8
-
-
0019979507
-
Microvascularspasm in the cardiomyopathic hamster: A preventable cause of focal myocardial necrosis
-
Factor, S.M., Minase, T., Cho, S., Dominitz, R., and Sonnenblick, E.H. (1982). Microvascularspasm in the cardiomyopathic hamster: a preventable cause of focal myocardial necrosis. Circulation 66, 342-354.
-
(1982)
Circulation
, vol.66
, pp. 342-354
-
-
Factor, S.M.1
Minase, T.2
Cho, S.3
Dominitz, R.4
Sonnenblick, E.H.5
-
9
-
-
0030870284
-
A treadmill exercise regimen for identifying cardiovascular phenotypes in transgenic mice
-
Fewell, J.G., Osinska, H., Klevitsky, R., Willie, N.G., Sfyris, G., Bahrehmand, F., and Robbins, J. (1997). A treadmill exercise regimen for identifying 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
Willie, N.G.4
Sfyris, G.5
Bahrehmand, F.6
Robbins, J.7
-
10
-
-
0032494165
-
Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin
-
Hack, A.A., Ly, C.T., Jiang, F., Clendenin, C.J., Sigrist, K.S., Wollmann, R.L., and McNally, E.M. (1998). Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin. J. Cell Biol. 142, 1279-1287.
-
(1998)
J. Cell Biol.
, vol.142
, pp. 1279-1287
-
-
Hack, A.A.1
Ly, C.T.2
Jiang, F.3
Clendenin, C.J.4
Sigrist, K.S.5
Wollmann, R.L.6
McNally, E.M.7
-
11
-
-
0029012453
-
Management of vasospastic angina-role of Nicorandil
-
Kaski, U.C. (1995). Management of vasospastic angina-role of Nicorandil. Cardiovasc. Drugs Ther. 9, 221-227.
-
(1995)
Cardiovasc. Drugs Ther.
, vol.9
, pp. 221-227
-
-
Kaski, U.C.1
-
12
-
-
0026698843
-
Molecular mechanism of action of Nicorandil
-
Kukovetz, W.R., Holzmann, S., and Poech, G. (1992). Molecular mechanism of action of Nicorandil. J. Cardiovasc. Pharmacol. 20, S1-S7.
-
(1992)
J. Cardiovasc. Pharmacol.
, vol.20
-
-
Kukovetz, W.R.1
Holzmann, S.2
Poech, G.3
-
13
-
-
0031722943
-
The sarcoglycan complex in limb-girdle muscular dystrophy
-
Lim, L.E., and Campbell, K.P. (1998). The sarcoglycan complex in limb-girdle muscular dystrophy. Curr. Opin. Neurol. 11, 443-452.
-
(1998)
Curr. Opin. Neurol.
, vol.11
, pp. 443-452
-
-
Lim, L.E.1
Campbell, K.P.2
-
14
-
-
0032912836
-
Heart involvement in muscular dystrophy due to sarcoglycan gene mutations
-
Melacini, P., Fanin, M., Duggan, D.J., Freda, M.P., Berardinelli, A., Danieli, G.A., Barchitta, A., Hoffman, E.P., Dalla Volta, S., and Angelini, C. (1999). Heart involvement in muscular dystrophy due to sarcoglycan gene mutations. Muscle Nerve 22, 473-479.
-
(1999)
Muscle Nerve
, vol.22
, pp. 473-479
-
-
Melacini, P.1
Fanin, M.2
Duggan, D.J.3
Freda, M.P.4
Berardinelli, A.5
Danieli, G.A.6
Barchitta, A.7
Hoffman, E.P.8
Dalla Volta, S.9
Angelini, C.10
-
15
-
-
0029738727
-
Disruption of muscle architecture and myocardial degeneration in mice lacking desmin
-
Milner, D.J., Weitzer, G., Tran, D., Bradley, A., and Capetanaki, Y. (1996). Disruption of muscle architecture and myocardial degeneration in mice lacking desmin. J. Cell Biol. 134, 1255-1270.
-
(1996)
J. Cell Biol.
, vol.134
, pp. 1255-1270
-
-
Milner, D.J.1
Weitzer, G.2
Tran, D.3
Bradley, A.4
Capetanaki, Y.5
-
16
-
-
0031764046
-
A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGM D2F) in Brazilian sarcoglycanopathies
-
Moreira, E.S., Vainzof, M., Marie, S.K., Nigro, V., Zatz, M., and Passos-Bueno, M.R. (1998). A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGM D2F) in Brazilian sarcoglycanopathies. J. Med. Genet. 35, 951-953.
-
(1998)
J. Med. Genet.
, vol.35
, pp. 951-953
-
-
Moreira, E.S.1
Vainzof, M.2
Marie, S.K.3
Nigro, V.4
Zatz, M.5
Passos-Bueno, M.R.6
-
17
-
-
0029816797
-
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene
-
Nigro, V., de Sa Moreira, E., Piluso, G., Vainzof, M., Belsito, A., Politano, L., Puca, A.A., Passos-Bueno, M.R., and Zatz, M. (1996). Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene. Nat. Genet. 14, 195-198.
-
(1996)
Nat. Genet.
, vol.14
, pp. 195-198
-
-
Nigro, V.1
De Sa Moreira, E.2
Piluso, G.3
Vainzof, M.4
Belsito, A.5
Politano, L.6
Puca, A.A.7
Passos-Bueno, M.R.8
Zatz, M.9
-
18
-
-
0028883973
-
Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy
-
Noguchi, S., McNally, E.M., Ben Othmane, K., Hagiwara, Y., Mizuno, Y., Yoshida, M., Yamamoto, H., Bonnemann, C.G., Gussoni, E., Denton, P.H., et al. (1995). Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy. Science 270, 819-822.
-
(1995)
Science
, vol.270
, pp. 819-822
-
-
Noguchi, S.1
McNally, E.M.2
Ben Othmane, K.3
Hagiwara, Y.4
Mizuno, Y.5
Yoshida, M.6
Yamamoto, H.7
Bonnemann, C.G.8
Gussoni, E.9
Denton, P.H.10
-
19
-
-
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
-
20
-
-
0027460658
-
Dystrophin protects the sarcolemma from stresses developed during muscle contraction
-
Petrof, B.J., Shrager, J.B., Stedman, H.H., Kelly, A.M., and Sweeney, H.L. (1993). Dystrophin protects the sarcolemma from stresses developed during muscle contraction. Proc. Natl. Acad. Sci. USA 90, 3710-3714.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 3710-3714
-
-
Petrof, B.J.1
Shrager, J.B.2
Stedman, H.H.3
Kelly, A.M.4
Sweeney, H.L.5
-
21
-
-
0028146869
-
Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy
-
Roberds, S.L., Leturcq, F., Allamand, V., Piccolo, F., Jeanpierre, M., Anderson, R.D., Lim, L.E., Lee, J.C., Tome, F.M., Romero, N.B., et al. (1994). Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy. Cell 78, 625-633.
-
(1994)
Cell
, vol.78
, pp. 625-633
-
-
Roberds, S.L.1
Leturcq, F.2
Allamand, V.3
Piccolo, F.4
Jeanpierre, M.5
Anderson, R.D.6
Lim, L.E.7
Lee, J.C.8
Tome, F.M.9
Romero, N.B.10
-
22
-
-
0032973716
-
Delineation of genomic deletion in cardiomyopathic hamster
-
Sakamoto, A., Abe, M., and Masaki, T. (1999). Delineation of genomic deletion in cardiomyopathic hamster. FEBS Lett. 447, 124-128.
-
(1999)
FEBS Lett.
, vol.447
, pp. 124-128
-
-
Sakamoto, A.1
Abe, M.2
Masaki, T.3
-
23
-
-
0030909575
-
M uscular dystrophies and the dystrophin-glycoprotein complex
-
Straub, V., and Campbell, K.P. (1997). M uscular dystrophies and the dystrophin-glycoprotein complex. Curr. Opin. Neurol. 10, 168-175.
-
(1997)
Curr. Opin. Neurol.
, vol.10
, pp. 168-175
-
-
Straub, V.1
Campbell, K.P.2
-
24
-
-
0033600605
-
∈-saicoglycan replaces α-sarcoglycan in smooth muscle to form a unique dystrophin-glycoprotein complex
-
in press
-
Straub V., Ettinger, A.J., Durbeej, M., Venzke, D.P., Cutshall, S., Sanes, J., and Campbell, K.P. (1999). ∈-saicoglycan replaces α-sarcoglycan in smooth muscle to form a unique dystrophin-glycoprotein complex. J. Biol. Chem., in press.
-
(1999)
J. Biol. Chem.
-
-
Straub, V.1
Ettinger, A.J.2
Durbeej, M.3
Venzke, D.P.4
Cutshall, S.5
Sanes, J.6
Campbell, K.P.7
-
25
-
-
0032006681
-
The role of cytoskeletal proteins in cardiomyopathies
-
Towbin, J.A. (1998). The role of cytoskeletal proteins in cardiomyopathies. Curr. Opin. Cell Biol. 10, 131-139.
-
(1998)
Curr. Opin. Cell Biol.
, vol.10
, pp. 131-139
-
-
Towbin, J.A.1
|