-
1
-
-
0024788014
-
Selective immunoreactivities of kidney basement membranes to monoclonal antibodies against laminin: Localization of the end of the long arm and the short arms to discrete microdomains
-
Abrahamson, D.R., M.H. Irwin, P.L. St. John, E.W. Perry, M.A. Accavitti, L.W. Heck, and J.R. Couchman. 1989. Selective immunoreactivities of kidney basement membranes to monoclonal antibodies against laminin: localization of the end of the long arm and the short arms to discrete microdomains. J. Cell Biol. 109:3477-3491.
-
(1989)
J. Cell Biol.
, vol.109
, pp. 3477-3491
-
-
Abrahamson, D.R.1
Irwin, M.H.2
St John, P.L.3
Perry, E.W.4
Accavitti, M.A.5
Heck, L.W.6
Couchman, J.R.7
-
2
-
-
0028579734
-
Perlecan, a basal lamina proteoglycan, promotes basic fibroblast growth factor-receptor binding, mitogenesis, and angiogenesis
-
Aviezer, D., D. Hecht, M. Safran, M. Eisinger, G. David, and A. Yayon. 1994. Perlecan, a basal lamina proteoglycan, promotes basic fibroblast growth factor-receptor binding, mitogenesis, and angiogenesis. Cell. 79:1005-1013.
-
(1994)
Cell
, vol.79
, pp. 1005-1013
-
-
Aviezer, D.1
Hecht, D.2
Safran, M.3
Eisinger, M.4
David, G.5
Yayon, A.6
-
3
-
-
0030480912
-
Localization of cranin (dystroglycan) at sites of cell-matrix and cell-cell contact: Recruitment to focal adhesion is dependent upon extracellular ligands
-
Belkin, A.M., and N.R. Smalheiser. 1996. Localization of cranin (dystroglycan) at sites of cell-matrix and cell-cell contact: recruitment to focal adhesion is dependent upon extracellular ligands. Cell Adhes. Commun. 4:281-296.
-
(1996)
Cell Adhes. Commun.
, vol.4
, pp. 281-296
-
-
Belkin, A.M.1
Smalheiser, N.R.2
-
4
-
-
0028170207
-
The regulation of α5β1 integrin expression in human muscle cells
-
Blaschuk, K.L., and P.C. Holland. 1994. The regulation of α5β1 integrin expression in human muscle cells. Dev. Biol. 164:475-483.
-
(1994)
Dev. Biol.
, vol.164
, pp. 475-483
-
-
Blaschuk, K.L.1
Holland, P.C.2
-
5
-
-
0031569896
-
Myoblast αvβ3 integrin levels are controlled by transcriptional regulation of expression of the β3 subunit and down-regulation of β3 subunit expression is required for skeletal muscle cell differentiation
-
Blaschuk, K.L., C. Guerin, and P.C. Holland. 1997. Myoblast αvβ3 integrin levels are controlled by transcriptional regulation of expression of the β3 subunit and down-regulation of β3 subunit expression is required for skeletal muscle cell differentiation. Dev. Biol. 184:266-277.
-
(1997)
Dev. Biol.
, vol.184
, pp. 266-277
-
-
Blaschuk, K.L.1
Guerin, C.2
Holland, P.C.3
-
6
-
-
0028971219
-
β-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex
-
Bönnemann, C.G., R. Modi, S. Noguchi, Y. Mizuno, M. Yoshida, E. Gussoni, E.M. McNally, D.J. Duggan, C. Angelini, E.P. Hoffman, et al. 1995. β-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex. Nat. Genet. 11:266-273.
-
(1995)
Nat. Genet.
, vol.11
, pp. 266-273
-
-
Bönnemann, C.G.1
Modi, R.2
Noguchi, S.3
Mizuno, Y.4
Yoshida, M.5
Gussoni, E.6
McNally, E.M.7
Duggan, D.J.8
Angelini, C.9
Hoffman, E.P.10
-
7
-
-
0028321841
-
Identification and purification of an agrin receptor from Torpedo post-synaptic membranes: A heterodimeric complex related to the dystroglycans
-
Bowe, M.A., K.A. Deyst, J.D. Leszyk, and J.R. Fallon. 1994. Identification and purification of an agrin receptor from Torpedo post-synaptic membranes: a heterodimeric complex related to the dystroglycans. Neuron. 12:1173-1180.
-
(1994)
Neuron
, vol.12
, pp. 1173-1180
-
-
Bowe, M.A.1
Deyst, K.A.2
Leszyk, J.D.3
Fallon, J.R.4
-
8
-
-
0029149471
-
Nitric oxide synthase is complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy
-
Brenman, J.E., D.S. Chao, H. Xia, K. Aldope, and D.S. Brendt. 1995. Nitric oxide synthase is complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy. Cell. 82:743-752.
-
(1995)
Cell
, vol.82
, pp. 743-752
-
-
Brenman, J.E.1
Chao, D.S.2
Xia, H.3
Aldope, K.4
Brendt, D.S.5
-
9
-
-
13344277364
-
Interaction of nitric oxide synthase with the postsynaptic density protein PSD-95 and α1-syntrophin mediated by PDZ domains
-
Brenman, J.E., D.S. Chao, S.H. Gee, A.W. McGee, S.E. Craven, D.R. Santillano, Z. Wu, F. Huang, H. Xia, M.F. Peters, et al. 1996. Interaction of nitric oxide synthase with the postsynaptic density protein PSD-95 and α1-syntrophin mediated by PDZ domains. Cell. 84:757-767.
-
(1996)
Cell
, vol.84
, pp. 757-767
-
-
Brenman, J.E.1
Chao, D.S.2
Gee, S.H.3
McGee, A.W.4
Craven, S.E.5
Santillano, D.R.6
Wu, Z.7
Huang, F.8
Xia, H.9
Peters, M.F.10
-
10
-
-
0028306787
-
A role for dystrophin associated glycoproteins and utrophin in agrin-induced AChR clustering
-
Campanelli, J.T., S.L. Roberds, K.P. Campbell, and R.H. Scheller. 1994. A role for dystrophin associated glycoproteins and utrophin in agrin-induced AChR clustering. Cell. 77:663-674.
-
(1994)
Cell
, vol.77
, pp. 663-674
-
-
Campanelli, J.T.1
Roberds, S.L.2
Campbell, K.P.3
Scheller, R.H.4
-
11
-
-
0028914964
-
Three muscular dystrophies: Loss of cytoskeleton-extra-cellular matrix linkage
-
Campbell, K.P. 1995. Three muscular dystrophies: loss of cytoskeleton-extra-cellular matrix linkage. Cell. 80:675-679.
-
(1995)
Cell
, vol.80
, pp. 675-679
-
-
Campbell, K.P.1
-
12
-
-
0024600620
-
Association of dystrophin and an integral membrane glycoprotein
-
Campbell, K.P., and S.D. Kahl. 1989. Association of dystrophin and an integral membrane glycoprotein. Nature. 338:259-262.
-
(1989)
Nature
, vol.338
, pp. 259-262
-
-
Campbell, K.P.1
Kahl, S.D.2
-
13
-
-
0028851913
-
The basement membrane of the neuromuscular junction: A synaptic mediatrix
-
Carbonetto, S., and M.H. Lindenbaum. 1995. The basement membrane of the neuromuscular junction: a synaptic mediatrix. Curr. Opin. Neurobiol. 5:596-605.
-
(1995)
Curr. Opin. Neurobiol.
, vol.5
, pp. 596-605
-
-
Carbonetto, S.1
Lindenbaum, M.H.2
-
14
-
-
0018351620
-
Duchenne muscular dystrophy: Plasma membrane loss initiates muscle cell necrosis unless it is repaired
-
Carpenter, S., and G. Karpati. 1979. Duchenne muscular dystrophy: plasma membrane loss initiates muscle cell necrosis unless it is repaired. Brain. 102: 147-161.
-
(1979)
Brain
, vol.102
, pp. 147-161
-
-
Carpenter, S.1
Karpati, G.2
-
15
-
-
16944365227
-
Mutational diversity and hot spots in the α-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)
-
Carrie, A., F. Piccolo, F. Leturcq, C. de Toma, K. Azibi, C. Beldjord, J.M. Vallat, L. Merlini, T. Voit, C. Sewry, et al. 1997. Mutational diversity and hot spots in the α-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D). J. Med. Genet. 34:470-475.
-
(1997)
J. Med. Genet.
, vol.34
, pp. 470-475
-
-
Carrie, A.1
Piccolo, F.2
Leturcq, F.3
De Toma, C.4
Azibi, K.5
Beldjord, C.6
Vallat, J.M.7
Merlini, L.8
Voit, T.9
Sewry, C.10
-
16
-
-
0031026624
-
Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve α-dystroglycan
-
Chiba, A., K. Matsumura, H. Yamada, T. Inazu, T. Shimizu, S. Kusunoki, I. Kanazawa, A. Kobata, and T. Endo. 1997. Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve α-dystroglycan. J. Biol. Chem. 272:2156-2162.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 2156-2162
-
-
Chiba, A.1
Matsumura, K.2
Yamada, H.3
Inazu, T.4
Shimizu, T.5
Kusunoki, S.6
Kanazawa, I.7
Kobata, A.8
Endo, T.9
-
17
-
-
0025173963
-
Correlation between fibronectin and its receptor in chick myoblast differentiation
-
Chung, C.Y., and M.-S. Kang. 1990. Correlation between fibronectin and its receptor in chick myoblast differentiation. J. Cell. Physiol. 142:392-400.
-
(1990)
J. Cell. Physiol.
, vol.142
, pp. 392-400
-
-
Chung, C.Y.1
Kang, M.-S.2
-
18
-
-
0028990431
-
Distribution of α-dystroglycan during embryonic nerve-muscle synaptogenesis
-
Cohen, M.W., C. Jacobson, E.W. Godfrey, K.P. Campbell, and S. Carbonetto. 1995. Distribution of α-dystroglycan during embryonic nerve-muscle synaptogenesis. J. Cell Biol. 129:1093-1101.
-
(1995)
J. Cell Biol.
, vol.129
, pp. 1093-1101
-
-
Cohen, M.W.1
Jacobson, C.2
Godfrey, E.W.3
Campbell, K.P.4
Carbonetto, S.5
-
19
-
-
0030968026
-
Laminin-induced clustering of dystroglycan on embryonic muscle cells: Comparison with agrin-induced clustering
-
Cohen, M.W., C. Jacobson, P.D. Yurchenco, G.E. Morris, and S. Carbonetto. 1997. Laminin-induced clustering of dystroglycan on embryonic muscle cells: comparison with agrin-induced clustering. J. Cell Biol. 136:1047-1058.
-
(1997)
J. Cell Biol.
, vol.136
, pp. 1047-1058
-
-
Cohen, M.W.1
Jacobson, C.2
Yurchenco, P.D.3
Morris, G.E.4
Carbonetto, S.5
-
20
-
-
0027247797
-
A new isoform of the laminin receptor α7β1 is developmentally regulated in skeletal muscle
-
Collo, G., L. Starr, and V. Quaranta. 1993. A new isoform of the laminin receptor α7β1 is developmentally regulated in skeletal muscle. J. Biol. Chem. 268: 19019-19024.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 19019-19024
-
-
Collo, G.1
Starr, L.2
Quaranta, V.3
-
21
-
-
0031451562
-
Sarcospan, the 25-kDa transmembrane component of the dystrophin-glyco-protein complex
-
Crosbie, R.H., J. Heighway, D.P. Venzke, J.C. Lee, and K.P. Campbell. 1997. Sarcospan, the 25-kDa transmembrane component of the dystrophin-glyco-protein 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, J.C.4
Campbell, K.P.5
-
22
-
-
0028260216
-
Elevated basic fibroblast growth factor in the serum of patients with Duchenne muscular dystrophy
-
D'Amore, P.A., R.H. Brown, Jr., P.T. Ku, E.P. Hoffman, H. Watanabe, K. Arahata, T. Ishihara, and J. Folkman. 1994. Elevated basic fibroblast growth factor in the serum of patients with Duchenne muscular dystrophy. Ann. Neurol. 35:362-365.
-
(1994)
Ann. Neurol.
, vol.35
, pp. 362-365
-
-
D'Amore, P.A.1
Brown R.H., Jr.2
Ku, P.T.3
Hoffman, E.P.4
Watanabe, H.5
Arahata, K.6
Ishihara, T.7
Folkman, J.8
-
23
-
-
0030975727
-
The A and B variants of the α3 integrin subunit: Tissue distribution and functional characterization
-
de Melker, A.A., L.M. Sterk, G.O. Delwel, D.L. Fles, H. Daams, J.J. Weening, and A. Sonnenberg. 1997. The A and B variants of the α3 integrin subunit: tissue distribution and functional characterization. Lab. Invest. 76:547-563.
-
(1997)
Lab. Invest.
, vol.76
, pp. 547-563
-
-
De Melker, A.A.1
Sterk, L.M.2
Delwel, G.O.3
Fles, D.L.4
Daams, H.5
Weening, J.J.6
Sonnenberg, A.7
-
24
-
-
0027090098
-
Co-localization and molecular association of dystrophin with laminin at the surface of mouse and human myotubes
-
Dickson, G., A. Azad., G.E. Morris, H. Simon, M. Noursadeghi, and F.S. Walsh. 1992. Co-localization and molecular association of dystrophin with laminin at the surface of mouse and human myotubes. J. Cell Sci. 103:1223-1233.
-
(1992)
J. Cell Sci.
, vol.103
, pp. 1223-1233
-
-
Dickson, G.1
Azad, A.2
Morris, G.E.3
Simon, H.4
Noursadeghi, M.5
Walsh, F.S.6
-
25
-
-
0023737217
-
Isolation and partial characterization of high affinity laminin receptors in neural cells
-
Douville, P.J., W.J. Harvey, and S. Carbonetto. 1988. Isolation and partial characterization of high affinity laminin receptors in neural cells. J. Biol. Chem. 263:14964-14969.
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 14964-14969
-
-
Douville, P.J.1
Harvey, W.J.2
Carbonetto, S.3
-
26
-
-
19244372467
-
Progressive muscular dystrophy in α-sarcoglycan-deficient mice
-
Duclos, F., V. Straub, S.A. Moore, D.P. Venzke, R.F. Hrstka, R.H. Crosbie, M. Durbeej, C.S. Lebakken, A.J. Ettinger, J. van der Meulen, et al. 1998. Progressive muscular dystrophy in α-sarcoglycan-deficient mice. J. Cell Biol. 142:1461-1471.
-
(1998)
J. Cell Biol.
, vol.142
, 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
-
27
-
-
0028979955
-
Non-muscle α-dystroglycan is involved in epithelial development
-
Durbeej, M., E. Larsson, O. Ibraghimov-Beskrovnaya, S.L. Roberds, K.P. Campbell, and P. Ekblom. 1995. Non-muscle α-dystroglycan is involved in epithelial development. J. Cell Biol. 130:79-91.
-
(1995)
J. Cell Biol.
, vol.130
, pp. 79-91
-
-
Durbeej, M.1
Larsson, E.2
Ibraghimov-Beskrovnaya, O.3
Roberds, S.L.4
Campbell, K.P.5
Ekblom, P.6
-
28
-
-
0025815479
-
Membrane organization of the dystrophin glycoprotein complex
-
Ervasti, J.M., and K.P. Campbell. 1991. Membrane organization of the dystrophin glycoprotein complex. Cell. 66:1121-1131.
-
(1991)
Cell
, vol.66
, pp. 1121-1131
-
-
Ervasti, J.M.1
Campbell, K.P.2
-
29
-
-
0027275643
-
A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin
-
Ervasti, J.M., and K.P. Campbell. 1993. A role for the dystrophin-glycoprotein 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
-
30
-
-
0023234520
-
A laminin substrate promotes myogenesis in rat skeletal muscle cultures: Analysis of replication and development using anti-desmin and anti-BrdUrd monoclonal antibodies
-
Foster, R.F., J.M. Thompson, and S.J. Kaufman. 1987. A laminin substrate promotes myogenesis in rat skeletal muscle cultures: analysis of replication and development using anti-desmin and anti-BrdUrd monoclonal antibodies. Dev. Biol. 122:11-20.
-
(1987)
Dev. Biol.
, vol.122
, pp. 11-20
-
-
Foster, R.F.1
Thompson, J.M.2
Kaufman, S.J.3
-
31
-
-
0027321171
-
Laminin-binding protein 120 from brain is closely related to the dystrophin-associated glycoprotein, dystroglycan, and binds with high affinity to the major heparin binding domain of laminin
-
Gee, S.H., R.W. Blacher, P.J. Douville, P.R. Provost, P.D. Yurchenco, and S. Carbonetto. 1993. Laminin-binding protein 120 from brain is closely related to the dystrophin-associated glycoprotein, dystroglycan, and binds with high affinity to the major heparin binding domain of laminin. J. Biol. Chem. 268: 14972-14980.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 14972-14980
-
-
Gee, S.H.1
Blacher, R.W.2
Douville, P.J.3
Provost, P.R.4
Yurchenco, P.D.5
Carbonetto, S.6
-
32
-
-
0028178082
-
Dystroglycan-α, a dystrophin-associated glycoprotein, is a functional agrin receptor
-
Gee, S.H., F. Montanaro, M.H. Lindenbaum, and S. Carbonetto. 1994. Dystroglycan-α, a dystrophin-associated glycoprotein, is a functional agrin receptor. Cell. 77:675-686.
-
(1994)
Cell
, vol.77
, pp. 675-686
-
-
Gee, S.H.1
Montanaro, F.2
Lindenbaum, M.H.3
Carbonetto, S.4
-
33
-
-
0027409341
-
In vitro and in vivo expression of α7 integrin and desmin define the primary and secondary myogenic lineages
-
George-Weinstein, M., R.F. Foster, J.V. Gerhart, and S.J. Kaufman. 1993. In vitro and in vivo expression of α7 integrin and desmin define the primary and secondary myogenic lineages. Dev. Biol. 156:209-229.
-
(1993)
Dev. Biol.
, vol.156
, pp. 209-229
-
-
George-Weinstein, M.1
Foster, R.F.2
Gerhart, J.V.3
Kaufman, S.J.4
-
34
-
-
15844380040
-
Agrin acts via a MuSK receptor complex
-
Glass, D.J., D.C. Bowen, T.N. Stitt, C. Radziejewski, J. Bruno, T.E. Ryan, D.R. Gies, S. Shah, K. Mattson, S.J. Burden, et al. 1996. Agrin acts via a MuSK receptor complex. Cell. 85:513-523.
-
(1996)
Cell
, vol.85
, pp. 513-523
-
-
Glass, D.J.1
Bowen, D.C.2
Stitt, T.N.3
Radziejewski, C.4
Bruno, J.5
Ryan, T.E.6
Gies, D.R.7
Shah, S.8
Mattson, K.9
Burden, S.J.10
-
35
-
-
0015847039
-
A new technique for the assay of infectivity of human adenovirus DNA
-
Graham, F.L., and A.J. Van der Eb. 1973. A new technique for the assay of infectivity of human adenovirus DNA. Virol. 52:456-467.
-
(1973)
Virol.
, vol.52
, pp. 456-467
-
-
Graham, F.L.1
Van Der Eb, A.J.2
-
36
-
-
0030772959
-
Role of focal adhesion kinase in integrin signaling
-
Guan, J.-L. 1997. Role of focal adhesion kinase in integrin signaling. Int. J. Biochem. 29:1085-1095.
-
(1997)
Int. J. Biochem.
, vol.29
, pp. 1085-1095
-
-
Guan, J.-L.1
-
37
-
-
0029127225
-
Analysis of fibronectin and vitronectin receptors on human fetal skeletal muscle cells upon differentiation
-
Gullberg, D., G. Sjoberg, T. Veiling, and T. Sejersen. 1995. Analysis of fibronectin and vitronectin receptors on human fetal skeletal muscle cells upon differentiation. Exp. Cell Res. 220:112-123.
-
(1995)
Exp. Cell Res.
, vol.220
, pp. 112-123
-
-
Gullberg, D.1
Sjoberg, G.2
Veiling, T.3
Sejersen, T.4
-
38
-
-
0032494165
-
γ-Sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin
-
Hack, A.A., C.L. Ly, F. Jiang, C.J. Clendenin, K.S. Sigrist, R.L. Wollmann, and E.M. McNally. 1998. γ-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.L.2
Jiang, F.3
Clendenin, C.J.4
Sigrist, K.S.5
Wollmann, R.L.6
McNally, E.M.7
-
39
-
-
0032445403
-
A role for dystroglycan in basement membrane assembly
-
Henry, M.D., and K.P. Campbell. 1998. A role for dystroglycan in basement membrane assembly. Cell. 95:859-870.
-
(1998)
Cell
, vol.95
, pp. 859-870
-
-
Henry, M.D.1
Campbell, K.P.2
-
40
-
-
0026543686
-
Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix
-
Ibraghimov-Beskrovnaya, O., J.M. Ervasti, C.J. Leveille, C.A. Slaughter, S.W. Sernett, and K.P. Campbell. 1992. Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix. Nature. 355:696-702.
-
(1992)
Nature
, vol.355
, pp. 696-702
-
-
Ibraghimov-Beskrovnaya, O.1
Ervasti, J.M.2
Leveille, C.J.3
Slaughter, C.A.4
Sernett, S.W.5
Campbell, K.P.6
-
41
-
-
0032529544
-
Alpha-dystroglycan functions in acetylcholine receptor aggregation but is not a coreceptor for agrin-MuSK signaling
-
Jacobson, C., F. Montanaro, M. Lindenbaum, S. Carbonetto, and M. Ferns. 1998. Alpha-dystroglycan functions in acetylcholine receptor aggregation but is not a coreceptor for agrin-MuSK signaling. J. Neurosci. 18:6340-6348.
-
(1998)
J. Neurosci.
, vol.18
, pp. 6340-6348
-
-
Jacobson, C.1
Montanaro, F.2
Lindenbaum, M.3
Carbonetto, S.4
Ferns, M.5
-
42
-
-
0028895952
-
Neuregulins are concentrated at nerve-muscle synapses and activate ACh-receptor gene expression
-
Jo, S.A., X. Zhu, M.A. Marchionni, and S.J. Burden. 1994. Neuregulins are concentrated at nerve-muscle synapses and activate ACh-receptor gene expression. Nature. 373:158-161.
-
(1994)
Nature
, vol.373
, pp. 158-161
-
-
Jo, S.A.1
Zhu, X.2
Marchionni, M.A.3
Burden, S.J.4
-
43
-
-
0028805790
-
Identification and characterization of the dystrophin anchoring site on β-dystroglycan
-
Jung, D., B. Yang, J. Meyer, J.S. Chamberlain, and K.P. Campbell. 1995. Identification and characterization of the dystrophin anchoring site on β-dystroglycan. J. Biol. Chem. 270:27305-27310.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 27305-27310
-
-
Jung, D.1
Yang, B.2
Meyer, J.3
Chamberlain, J.S.4
Campbell, K.P.5
-
44
-
-
10544235436
-
Characterization of δ-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy
-
Jung, D., F. Duclos, B. Apostol, V. Straub, J.C. Lee, V. Allamand, D.P. Venzke, Y. Sunada, C.R. Moomaw, C.J. Leveille, et al. 1996a. Characterization of δ-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy. J. Biol. Chem. 271:32321-32329.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 32321-32329
-
-
Jung, D.1
Duclos, F.2
Apostol, B.3
Straub, V.4
Lee, J.C.5
Allamand, V.6
Venzke, D.P.7
Sunada, Y.8
Moomaw, C.R.9
Leveille, C.J.10
-
45
-
-
18544402590
-
Absence of γ-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12
-
Jung, D., F. Leturcq, Y. Sunada, F. Duclos, F.M S. Tome, C. Moomaw, L. Merlini, K. Azibi, M. Chaouch, C. Slaughter, et al. 1996b. Absence of γ-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12. FEBS Lett. 381:15-20.
-
(1996)
FEBS Lett.
, vol.381
, pp. 15-20
-
-
Jung, D.1
Leturcq, F.2
Sunada, Y.3
Duclos, F.4
Tome, F.M.S.5
Moomaw, C.6
Merlini, L.7
Azibi, K.8
Chaouch, M.9
Slaughter, C.10
-
46
-
-
0027533969
-
Dystrophin-glycoprotein complex and laminin colocalize to the sarcolemma and transverse tubules of cardiac muscle
-
Klietsch, R., J.M. Ervasti, W. Arnold, K.P. Campbell, and A.O. Jorgensen. 1993. Dystrophin-glycoprotein complex and laminin colocalize to the sarcolemma and transverse tubules of cardiac muscle. Circ. Res. 72:349-360.
-
(1993)
Circ. Res.
, vol.72
, pp. 349-360
-
-
Klietsch, R.1
Ervasti, J.M.2
Arnold, W.3
Campbell, K.P.4
Jorgensen, A.O.5
-
47
-
-
0027096011
-
Non-coordinate developmental regulation of N-cadherin, N-CAM, integrin, and fibronectin mRNA levels during myoblast terminal differentiation
-
MacCalman, C.D., N. Bardeesy, P.C. Holland, and O.W. Blaschuk. 1992. Non-coordinate developmental regulation of N-cadherin, N-CAM, integrin, and fibronectin mRNA levels during myoblast terminal differentiation. Dev. Dyn. 195:127-132.
-
(1992)
Dev. Dyn.
, vol.195
, pp. 127-132
-
-
MacCalman, C.D.1
Bardeesy, N.2
Holland, P.C.3
Blaschuk, O.W.4
-
48
-
-
0028817970
-
Visualization of dystrophic muscle fibers in mdx mouse by vital staining with Evans blue: Evidence of apoptosis indystrophin-deficient muscle
-
Matsuda, R., A. Nishikawa, and H. Tanaka 1995. Visualization of dystrophic muscle fibers in mdx mouse by vital staining with Evans blue: evidence of apoptosis indystrophin-deficient muscle. J. Biochem. 118:959-964.
-
(1995)
J. Biochem.
, vol.118
, pp. 959-964
-
-
Matsuda, R.1
Nishikawa, A.2
Tanaka, H.3
-
49
-
-
0030724952
-
Absence of integrin α7 causes a new form of muscular dystrophy
-
Mayer, U., G. Saher, R. Fässler, A. Bornemann, F. Echtermeyer, H. von der Mark, N. Miosge, E. Pöschl, and K. von der Mark. 1997. Absence of integrin α7 causes a new form of muscular dystrophy. Nat. Genet. 17:318-323.
-
(1997)
Nat. Genet.
, vol.17
, pp. 318-323
-
-
Mayer, U.1
Saher, G.2
Fässler, R.3
Bornemann, A.4
Echtermeyer, F.5
Von Der Mark, H.6
Miosge, N.7
Pöschl, E.8
Von Der Mark, K.9
-
50
-
-
0032559065
-
Human ε-sarcoglycan is highly related to α-sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene
-
McNally, E.M., C.T. Ly, and L.M. Kunkel. 1998. Human ε-sarcoglycan is highly related to α-sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene. FEBS Lett. 422:27-32.
-
(1998)
FEBS Lett.
, vol.422
, pp. 27-32
-
-
McNally, E.M.1
Ly, C.T.2
Kunkel, L.M.3
-
51
-
-
0030610896
-
Laminin α2 chain-null mutant mice by targeted disruption of the Lama2 gene: A new model of merosin (laminin-2)-deficient congenital muscular dystrophy
-
Miyagoe, Y., K. Hanaoka, I. Nonaka, M. Hayasaka, Y. Nabeshima, K. Arahata, Y. Nabeshima, and S. Takeda. 1997. Laminin α2 chain-null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin-2)-deficient congenital muscular dystrophy. FEBS Lett. 415:33-39.
-
(1997)
FEBS Lett.
, vol.415
, pp. 33-39
-
-
Miyagoe, Y.1
Hanaoka, K.2
Nonaka, I.3
Hayasaka, M.4
Nabeshima, Y.5
Arahata, K.6
Nabeshima, Y.7
Takeda, S.8
-
52
-
-
0032519864
-
Laminin and α-dystroglycan mediate acetylcholine receptor aggregation via a MuSK-independent pathway
-
Montanaro, F., S.H. Gee, C. Jacobson, M.H. Lindenbaum, and S. Carbonetto. 1998. Laminin and α-dystroglycan mediate acetylcholine receptor aggregation via a MuSK-independent pathway. J. Neurosci. 18:1250-1260.
-
(1998)
J. Neurosci.
, vol.18
, pp. 1250-1260
-
-
Montanaro, F.1
Gee, S.H.2
Jacobson, C.3
Lindenbaum, M.H.4
Carbonetto, S.5
-
53
-
-
0029816797
-
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ-sarcoglycan gene
-
Nigro, V., E. de Sa Moreira, G. Piluso, M. Vainzof, A. Belsito, L. Politano, A.A. Puca, M.R. Passos-Bueno, and M. Zatz. 1996. Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ-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
-
54
-
-
0028883973
-
Mutations in the dystrophin-associated protein γ-sarcoglycan in chromosome 13 muscular dystrophy
-
Noguchi, S., E.M. McNelly, K.B. Othmane, Y. Hagiwara, Y. Mizuno, M. Yoshida, H. Yamamoto, C.G. Bönnemann, E. Gussoni, P.H. Denton, et al. 1995. Mutations in the dystrophin-associated protein γ-sarcoglycan in chromosome 13 muscular dystrophy. Science. 270:819-822.
-
(1995)
Science
, vol.270
, pp. 819-822
-
-
Noguchi, S.1
McNelly, E.M.2
Othmane, K.B.3
Hagiwara, Y.4
Mizuno, Y.5
Yoshida, M.6
Yamamoto, H.7
Bönnemann, C.G.8
Gussoni, E.9
Denton, P.H.10
-
55
-
-
0023875632
-
Laminin alters cell shape and stimulates motility and proliferation of murine skeletal myoblasts
-
Öcalan, M., S.L. Goodman, U. Kühl, S.D. Hauschka, and K. von der Mark. 1988. Laminin alters cell shape and stimulates motility and proliferation of murine skeletal myoblasts. Dev. Biol. 125:158-167.
-
(1988)
Dev. Biol.
, vol.125
, pp. 158-167
-
-
Öcalan, M.1
Goodman, S.L.2
Kühl, U.3
Hauschka, S.D.4
Von Der Mark, K.5
-
56
-
-
0026067790
-
Dystrophin-glycoprotein complex is highly enriched in isolated skeletal muscle sarcolemma
-
Ohlendieck, K., J.M. Ervasti, J.B. Snook, and K.P. Campbell. 1991. Dystrophin-glycoprotein complex is highly enriched in isolated skeletal muscle sarcolemma. J. Cell Biol. 112:135-148.
-
(1991)
J. Cell Biol.
, vol.112
, pp. 135-148
-
-
Ohlendieck, K.1
Ervasti, J.M.2
Snook, J.B.3
Campbell, K.P.4
-
57
-
-
0027520443
-
Sequence and tissue distribution of the integrin α9 subunit, a novel partner of β1 that is widely distributed in epithelia and muscle
-
Palmer, E.L., C. Ruegg, R. Ferrano, R. Pytela, and D. Sheppard. 1993. Sequence and tissue distribution of the integrin α9 subunit, a novel partner of β1 that is widely distributed in epithelia and muscle. J. Cell Biol. 123:1289-1297.
-
(1993)
J. Cell Biol.
, vol.123
, pp. 1289-1297
-
-
Palmer, E.L.1
Ruegg, C.2
Ferrano, R.3
Pytela, R.4
Sheppard, D.5
-
58
-
-
0031456144
-
Distribution and function of laminins in the neuromuscular system of the developing, adult, and mutant mice
-
Patton, B.L., J.H. Miner, A.Y. Chiu, and J.R. Sanes. 1997. Distribution and function of laminins in the neuromuscular system of the developing, adult, and mutant mice. J. Cell Biol. 139:1507-1521.
-
(1997)
J. Cell Biol.
, vol.139
, pp. 1507-1521
-
-
Patton, B.L.1
Miner, J.H.2
Chiu, A.Y.3
Sanes, J.R.4
-
59
-
-
0031770342
-
The relationship between perlecan and dystroglycan and its implication in the formation of the neuromuscular junction
-
Peng, H.B., A.A. Ali, D.F. Daggett, H. Rauvala, J.R. Hassell, and N.R. Smalheiser. 1998. The relationship between perlecan and dystroglycan and its implication in the formation of the neuromuscular junction. Cell Adhes. Commun. 5:475-489.
-
(1998)
Cell Adhes. Commun.
, vol.5
, pp. 475-489
-
-
Peng, H.B.1
Ali, A.A.2
Daggett, D.F.3
Rauvala, H.4
Hassell, J.R.5
Smalheiser, N.R.6
-
60
-
-
0017613512
-
A simplification of the protein assay method of Lowry et al. which is more generally applicable
-
Peterson, G.L. 1977. A simplification of the protein assay method of Lowry et al. which is more generally applicable. Anal. Biochem. 83:346-356.
-
(1977)
Anal. Biochem.
, vol.83
, pp. 346-356
-
-
Peterson, G.L.1
-
61
-
-
0028146869
-
Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy
-
Roberds, S.L., F. Leturcq, V. Allamand, F. Piccolo, M. Jeanpierre, R.D. Anderson, L.E. Lim, J.C. Lee, F.M.S. Tomé, N.B. Romero, 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
Tomé, F.M.S.9
Romero, N.B.10
-
62
-
-
0024850505
-
Serum enzymes in disease of skeletal muscle
-
Rosalki, S.B. 1989. Serum enzymes in disease of skeletal muscle. Clin. Lab. Med. 9:767-781.
-
(1989)
Clin. Lab. Med.
, vol.9
, pp. 767-781
-
-
Rosalki, S.B.1
-
63
-
-
0026708853
-
Roles for the integrin VLA-4 and its counter receptor VCAM-1 in myogenesis
-
Rosen, G.D., J.R. Sanes, R. LaChance, J.M. Cunningham, J. Roman, and D.C. Dean. 1992. Roles for the integrin VLA-4 and its counter receptor VCAM-1 in myogenesis. Cell. 69:1107-1119.
-
(1992)
Cell
, vol.69
, pp. 1107-1119
-
-
Rosen, G.D.1
Sanes, J.R.2
LaChance, R.3
Cunningham, J.M.4
Roman, J.5
Dean, D.C.6
-
64
-
-
0004136246
-
-
Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY. Section 1.53
-
Sambrook, J., E.F. Fritsch, and T. Maniatis. 1989. Molecular Cloning. A Laboratory Manual. 2nd Edition. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY. Section 1.53.
-
(1989)
Molecular Cloning. A Laboratory Manual. 2nd Edition
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
65
-
-
0025010542
-
Molecular heterogeneity of basal laminae: Isoforms of laminin and collagen IV at the neuromuscular junction and elsewhere
-
Sanes, J.R., E. Engvall, R. Butkowski, and D.D. Hunter. 1990. Molecular heterogeneity of basal laminae: isoforms of laminin and collagen IV at the neuromuscular junction and elsewhere. J. Cell Biol. 111:1685-1699.
-
(1990)
J. Cell Biol.
, vol.111
, pp. 1685-1699
-
-
Sanes, J.R.1
Engvall, E.2
Butkowski, R.3
Hunter, D.D.4
-
66
-
-
0029664439
-
Integrin subunit ratios, cytoplasmic domains, and growth factor synergy regulate muscle proliferation and differentiation
-
Sastry, S.K., M. Lakonishok, D.A. Thomas, J. Muschler, and A.F. Horwitz. 1996. Integrin subunit ratios, cytoplasmic domains, and growth factor synergy regulate muscle proliferation and differentiation. J. Cell Biol. 133:169-184.
-
(1996)
J. Cell Biol.
, vol.133
, pp. 169-184
-
-
Sastry, S.K.1
Lakonishok, M.2
Thomas, D.A.3
Muschler, J.4
Horwitz, A.F.5
-
67
-
-
0024836467
-
Cellular distribution of smooth muscle actins during mammalian embryogenesis: Expression of the α-vascular but not the γ-enteric isoform in differentiating striated myocytes
-
Sawtell, N.M., and J.L. Lessard. 1989. Cellular distribution of smooth muscle actins during mammalian embryogenesis: expression of the α-vascular but not the γ-enteric isoform in differentiating striated myocytes. J. Cell Biol. 109:2929-2937.
-
(1989)
J. Cell Biol.
, vol.109
, pp. 2929-2937
-
-
Sawtell, N.M.1
Lessard, J.L.2
-
68
-
-
0029582766
-
Expression of laminin isoforms in mouse myogenic cells in vitro and in vivo
-
Schuler, F., and L.M. Sorokin. 1995. Expression of laminin isoforms in mouse myogenic cells in vitro and in vivo. J. Cell Sci. 108:3795-3805.
-
(1995)
J. Cell Sci.
, vol.108
, pp. 3795-3805
-
-
Schuler, F.1
Sorokin, L.M.2
-
69
-
-
0031310941
-
An orphan receptor tyrosine kinase family whose members serve as nonintegrin collagen receptors
-
Shrivastava, A., C. Radziejewski, E. Campbell, L. Kovac, M. McGlynn, T.E. Ryan, S. Davies, M.P. Goldfarb, D.J. Glass, G. Lemke, and G.D. Yancopoulos. 1997. An orphan receptor tyrosine kinase family whose members serve as nonintegrin collagen receptors. Mol. Cell. 1:25-34.
-
(1997)
Mol. Cell
, vol.1
, pp. 25-34
-
-
Shrivastava, A.1
Radziejewski, C.2
Campbell, E.3
Kovac, L.4
McGlynn, M.5
Ryan, T.E.6
Davies, S.7
Goldfarb, M.P.8
Glass, D.J.9
Lemke, G.10
Yancopoulos, G.D.11
-
70
-
-
0023410821
-
Cranin, a laminin-binding protein of cell membranes
-
Smalheiser, N.R., and N.B. Schwartz. 1987. Cranin, a laminin-binding protein of cell membranes. Proc. Natl. Acad. Sci. USA. 84:6457-6461.
-
(1987)
Proc. Natl. Acad. Sci. USA
, vol.84
, pp. 6457-6461
-
-
Smalheiser, N.R.1
Schwartz, N.B.2
-
71
-
-
0029072703
-
Purification of cranin, a laminin-binding membrane protein: Identity with dystroglycan and reassessment of its carbohydrate moieties
-
Smalheiser, N.R., and E. Kim. 1995. Purification of cranin, a laminin-binding membrane protein: identity with dystroglycan and reassessment of its carbohydrate moieties. J. Biol. Chem. 270:15425-15433.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 15425-15433
-
-
Smalheiser, N.R.1
Kim, E.2
-
72
-
-
0031010857
-
Myonuclear apoptosis in dystrophic mdx muscle occurs by perforin-mediated cytotoxicity
-
Spencer, M.J., C.M. Walsh, K.A. Dorshkind, E.M. Rodriguez, and J.T. Tidball. 1997. Myonuclear apoptosis in dystrophic mdx muscle occurs by perforin-mediated cytotoxicity. J. Clin. Invest. 99:2745-2751.
-
(1997)
J. Clin. Invest.
, vol.99
, pp. 2745-2751
-
-
Spencer, M.J.1
Walsh, C.M.2
Dorshkind, K.A.3
Rodriguez, E.M.4
Tidball, J.T.5
-
73
-
-
0030783172
-
Animal models for muscular dystrophy show different patterns of sarcolemmal disruption
-
Straub, V., J.A. Rafael, J.S. Chamberlain, and K.P. Campbell. 1997. Animal models for muscular dystrophy show different patterns of sarcolemmal disruption. J. Cell Biol. 139:375-385.
-
(1997)
J. Cell Biol.
, vol.139
, pp. 375-385
-
-
Straub, V.1
Rafael, J.A.2
Chamberlain, J.S.3
Campbell, K.P.4
-
74
-
-
0030038229
-
Suppression of p53 activity and p21WAF1/CIP1 expression by vascular cell integrin αvβ3 during angiogenesis
-
Stromblad, S., J.C. Becker, M. Yebra, P.C. Brooks, and D.A. Cheresh. 1996. Suppression of p53 activity and p21WAF1/CIP1 expression by vascular cell integrin αvβ3 during angiogenesis. J. Clin. Invest. 98:426-433.
-
(1996)
J. Clin. Invest.
, vol.98
, pp. 426-433
-
-
Stromblad, S.1
Becker, J.C.2
Yebra, M.3
Brooks, P.C.4
Cheresh, D.A.5
-
75
-
-
0027941192
-
Dystroglycan binds nerve and muscle agrin
-
Sugiyama, J., D.C. Bowen, and Z.W. Hall. 1994. Dystroglycan binds nerve and muscle agrin. Neuron. 13:103-115.
-
(1994)
Neuron
, vol.13
, pp. 103-115
-
-
Sugiyama, J.1
Bowen, D.C.2
Hall, Z.W.3
-
77
-
-
0028206868
-
Molecular organization at the glycoprotein-complex-binding site of dystrophin
-
Suzuki, A., M. Yoshida, K. Hayashi, Y. Mizuno, Y. Hagiwara, and E. Ozawa. 1994. Molecular organization at the glycoprotein-complex-binding site of dystrophin. Eur. J. Biochem. 220:283-292.
-
(1994)
Eur. J. Biochem.
, vol.220
, pp. 283-292
-
-
Suzuki, A.1
Yoshida, M.2
Hayashi, K.3
Mizuno, Y.4
Hagiwara, Y.5
Ozawa, E.6
-
78
-
-
0025296349
-
α1β1 integrin heterodimer functions as dual laminin/collagen receptor in neural cells
-
Tawil, N., M. Houde, R. Blacher, F. Esch, L.F. Reichardt, D.C. Turner, and S. Carbonetto. 1990. α1β1 integrin heterodimer functions as dual laminin/collagen receptor in neural cells. Biochemistry. 29:6450-6544.
-
(1990)
Biochemistry
, vol.29
, pp. 6450-6544
-
-
Tawil, N.1
Houde, M.2
Blacher, R.3
Esch, F.4
Reichardt, L.F.5
Turner, D.C.6
Carbonetto, S.7
-
79
-
-
0030742809
-
DNA-fragmentation and expression of apoptosis-related proteins in muscular dystrophies
-
Tews, D.S., and H.H. Goebel. 1997. DNA-fragmentation and expression of apoptosis-related proteins in muscular dystrophies. Neuropath. Appl. Neurobiol. 23:331-338.
-
(1997)
Neuropath. Appl. Neurobiol.
, vol.23
, pp. 331-338
-
-
Tews, D.S.1
Goebel, H.H.2
-
80
-
-
0030462678
-
Dystroglycan in the cerebellum is a laminin α2-chain binding protein at the glial-vascular interface and is expressed in Purkinje cells
-
Tian, M., C. Jacobson, S.H. Gee, K.P. Campbell, S. Carbonetto, and M. Jucker. 1996. Dystroglycan in the cerebellum is a laminin α2-chain binding protein at the glial-vascular interface and is expressed in Purkinje cells. Eur. J. Neurosci. 8:2739-2747.
-
(1996)
Eur. J. Neurosci.
, vol.8
, pp. 2739-2747
-
-
Tian, M.1
Jacobson, C.2
Gee, S.H.3
Campbell, K.P.4
Carbonetto, S.5
Jucker, M.6
-
81
-
-
0029034975
-
Apoptosis precedes necrosis in dystrophin-deficienl muscle
-
Tidball, J.G., D.E. Albrecht, B.E. Lokensgard, and M.J. Spencer. 1995. Apoptosis precedes necrosis in dystrophin-deficienl muscle. J. Cell Sci. 108:2197-2204.
-
(1995)
J. Cell Sci.
, vol.108
, pp. 2197-2204
-
-
Tidball, J.G.1
Albrecht, D.E.2
Lokensgard, B.E.3
Spencer, M.J.4
-
82
-
-
0020014992
-
Laminin
-
Timpl, R., H. Rohde, L. Risteli, U. Ott, P.G. Robey, and G.R. Martin. 1982. Laminin. Methods Enzymol. 82:831-838.
-
(1982)
Methods Enzymol.
, vol.82
, pp. 831-838
-
-
Timpl, R.1
Rohde, H.2
Risteli, L.3
Ott, U.4
Robey, P.G.5
Martin, G.R.6
-
83
-
-
0029794008
-
Merosin and laminin in myogenesis; requirement for merosin in myotube stability and survival
-
Vachon, P.M., F. Loechel, H. Xu, U.M. Wewer, and E. Engvall. 1996. Merosin and laminin in myogenesis; requirement for merosin in myotube stability and survival. J. Cell Biol. 134:1483-1479.
-
(1996)
J. Cell Biol.
, vol.134
, pp. 1483-11479
-
-
Vachon, P.M.1
Loechel, F.2
Xu, H.3
Wewer, U.M.4
Engvall, E.5
-
84
-
-
0030610576
-
1) in muscle function and survival: Disrupted expression in merosin-deficient congenital muscular dystrophy
-
1) in muscle function and survival: disrupted expression in merosin-deficient congenital muscular dystrophy. J. Clin. Invest. 100:1870-1881.
-
(1997)
J. Clin. Invest.
, vol.100
, pp. 1870-1881
-
-
Vachon, P.M.1
Xu, H.2
Liu, L.3
Loechel, F.4
Hayashi, Y.5
Arahata, K.6
Reed, J.C.7
Wewer, U.8
Engvall, E.9
-
85
-
-
0031309902
-
The discoidin domain receptor tyrosine kinases are activated by collagen
-
Vogel, W., G.D. Gish, F. Alves, and T. Pawson. 1997. The discoidin domain receptor tyrosine kinases are activated by collagen. Mol. Cell. 1:13-23.
-
(1997)
Mol. Cell
, vol.1
, pp. 13-23
-
-
Vogel, W.1
Gish, G.D.2
Alves, F.3
Pawson, T.4
-
86
-
-
0024359714
-
The differentiation and redifferentiation of myoblasts is triggered by fibronectin and laminin
-
von der Mark, H., and M. Öcalan. 1989. The differentiation and redifferentiation of myoblasts is triggered by fibronectin and laminin. Differentiation. 40: 150-157.
-
(1989)
Differentiation
, vol.40
, pp. 150-157
-
-
Von Der Mark, H.1
Öcalan, M.2
-
87
-
-
0346222463
-
DNA mediated transfer of the adenine-phosphoribosyltransferase locus into mammalian cells
-
Wigler, M., A. Pellicer, S. Silverstein, R. Axel, G. Urlaub, and L. Chasin. 1979. DNA mediated transfer of the adenine-phosphoribosyltransferase locus into mammalian cells. Proc. Natl. Acad. Sci. USA. 76:1373-1376.
-
(1979)
Proc. Natl. Acad. Sci. USA
, vol.76
, pp. 1373-1376
-
-
Wigler, M.1
Pellicer, A.2
Silverstein, S.3
Axel, R.4
Urlaub, G.5
Chasin, L.6
-
88
-
-
0030927063
-
Dystroglycan is essential for early embryonic development: Disruption of Reichert's membrane in DAG1-null mice
-
Williamson, R.A., M.D. Henry, K.J. Daniels, R.F. Hrstka, J.C. Lee, Y. Sunada, O. Ibraghimov-Beskrovnaya, and K.P. Campbell. 1997. Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in DAG1-null mice. Human Mol. Genet. 6:831-841.
-
(1997)
Human Mol. Genet.
, vol.6
, pp. 831-841
-
-
Williamson, R.A.1
Henry, M.D.2
Daniels, K.J.3
Hrstka, R.F.4
Lee, J.C.5
Sunada, Y.6
Ibraghimov-Beskrovnaya, O.7
Campbell, K.P.8
-
89
-
-
0028877455
-
Muscular dystrophies: Diseases of the dystrophin-glycoprotein complex
-
Worton, R. 1995. Muscular dystrophies: Diseases of the dystrophin-glycoprotein complex. Science. 270:755-756.
-
(1995)
Science
, vol.270
, pp. 755-756
-
-
Worton, R.1
-
90
-
-
0028334735
-
Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse
-
Xu, H., P. Christmas, X.-R. Wu, U.M. Wewer, and E. Engvall. 1994. Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse. Proc. Natl. Acad. Sci. USA. 91:5572-5576.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 5572-5576
-
-
Xu, H.1
Christmas, P.2
Wu, X.-R.3
Wewer, U.M.4
Engvall, E.5
-
91
-
-
0027930113
-
Dystroglycan is a binding protein of laminin and merosin in peripheral nerve
-
Yamada, H., T. Shimizu, T. Tanaka, K.P. Campbell, and K. Matsumura. 1994. Dystroglycan is a binding protein of laminin and merosin in peripheral nerve. FEBS Lett. 352:49-53.
-
(1994)
FEBS Lett.
, vol.352
, pp. 49-53
-
-
Yamada, H.1
Shimizu, T.2
Tanaka, T.3
Campbell, K.P.4
Matsumura, K.5
-
92
-
-
0029664729
-
Characterization of dystroglycan-laminin interaction in peripheral nerve
-
Yamada, H., A. Chiba, T. Endo, A. Kobata, L.V.B. Anderson, H. Hori, H. Fukuta-Ohi. I. Kanazawa, K.P. Campbell, T. Shimizu, and K. Matsumura 1996. Characterization of dystroglycan-laminin interaction in peripheral nerve. J. Neurochem. 66:1518-1524.
-
(1996)
J. Neurochem.
, vol.66
, pp. 1518-1524
-
-
Yamada, H.1
Chiba, A.2
Endo, T.3
Kobata, A.4
Anderson, L.V.B.5
Hori, H.6
Fukuta-Ohi, H.7
Kanazawa, I.8
Campbell, K.P.9
Shimizu, T.10
Matsumura, K.11
-
93
-
-
0029013870
-
SH3 domain-mediated interaction of dystroglycan and Grb2
-
Yang, B., D. Jung, D. Motto, J. Meyer, G. Koretzky, and K.P. Campbell. 1995. SH3 domain-mediated interaction of dystroglycan and Grb2. J. Biol. Chem. 270:1-4.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 1-4
-
-
Yang, B.1
Jung, D.2
Motto, D.3
Meyer, J.4
Koretzky, G.5
Campbell, K.P.6
-
94
-
-
0025242185
-
Glycoprotein complex anchoring dystrophin to sarcolemma
-
Yoshida, M., and E. Ozawa. 1990. Glycoprotein complex anchoring dystrophin to sarcolemma. J. Biochem. (Tokyo). 108:748-752.
-
(1990)
J. Biochem. (Tokyo)
, vol.108
, pp. 748-752
-
-
Yoshida, M.1
Ozawa, E.2
-
95
-
-
0028302369
-
Dissociation of the complex of dystrophin and its associated proteins into several unique groups by n-octyl-D-glucoside
-
Yoshida, M., A. Suzuki, H. Yamamoto, S. Noguchi, Y. Mizuno, and E. Ozawa. 1994. Dissociation of the complex of dystrophin and its associated proteins into several unique groups by n-octyl-D-glucoside. Eur. J. Biochem. 222: 1055-1061.
-
(1994)
Eur. J. Biochem.
, vol.222
, pp. 1055-1061
-
-
Yoshida, M.1
Suzuki, A.2
Yamamoto, H.3
Noguchi, S.4
Mizuno, Y.5
Ozawa, E.6
-
96
-
-
0031939073
-
Bidirectional signaling between sarcoglycans and the integrin adhesion system in cultured L6 myocytes
-
Yoshida, T., Y. Pan, H. Hanada, Y. Iwata, and M. Shigekawa. 1998. Bidirectional signaling between sarcoglycans and the integrin adhesion system in cultured L6 myocytes. J. Biol. Chem. 273:1583-1590.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 1583-1590
-
-
Yoshida, T.1
Pan, Y.2
Hanada, H.3
Iwata, Y.4
Shigekawa, M.5
-
97
-
-
0027159464
-
Increased expression of the 43-kD protein disrupts acetylcholine receptor clustering in myotubes
-
Yoshihara, C.M., and Z.W. Hall. 1993. Increased expression of the 43-kD protein disrupts acetylcholine receptor clustering in myotubes. J. Cell Biol. 122: 169-179.
-
(1993)
J. Cell Biol.
, vol.122
, pp. 169-179
-
-
Yoshihara, C.M.1
Hall, Z.W.2
-
98
-
-
0028983407
-
The α5β1 integrin supports survival of cells on fibronectin and up-regulates Bcl-2 expression
-
Zhang, Z., K. Vuori, J.C. Reed, and E. Ruoslahti. 1995. The α5β1 integrin supports survival of cells on fibronectin and up-regulates Bcl-2 expression. Proc. Natl. Acad. Sci. USA. 92:6161-6165.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 6161-6165
-
-
Zhang, Z.1
Vuori, K.2
Reed, J.C.3
Ruoslahti, E.4
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