-
1
-
-
17844377334
-
Echocardiographic and electrocardiographic ndings of cardiomyopathy in Duchenne and Becker-Kiener muscular dystrophies
-
Kirchmann, C., Kececioglu, D., Korinthenberg, R. and Dittrich, S. (2005) Echocardiographic and electrocardiographic ndings of cardiomyopathy in Duchenne and Becker-Kiener muscular dystrophies. Pediatr. Cardiol., 26, 66-72.
-
(2005)
Pediatr. Cardiol.
, vol.26
, pp. 66-72
-
-
Kirchmann, C.1
Kececioglu, D.2
Korinthenberg, R.3
Dittrich, S.4
-
2
-
-
0029970718
-
Cardiac dysfunction with Becker muscular dystrophy
-
Saito, M., Kawai, H., Akaike, M., Adachi, K., Nishida, Y. and Saito, S. (1996) Cardiac dysfunction with Becker muscular dystrophy. Am. Heart J., 132, 642-647.
-
(1996)
Am. Heart J.
, vol.132
, pp. 642-647
-
-
Saito, M.1
Kawai, H.2
Akaike, M.3
Adachi, K.4
Nishida, Y.5
Saito, S.6
-
3
-
-
0033818186
-
Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy
-
Tsubata, S., Bowles, K.R., Vatta, M., Zintz, C., Titus, J., Muhonen, L., Bowles, N.E. and Towbin, J.A. (2000) Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy. J. Clin. Invest., 106, 655-662.
-
(2000)
J. Clin. Invest.
, vol.106
, pp. 655-662
-
-
Tsubata, S.1
Bowles, K.R.2
Vatta, M.3
Zintz, C.4
Titus, J.5
Muhonen, L.6
Bowles, N.E.7
Towbin, J.A.8
-
4
-
-
33745310936
-
Cardiac involvement in Fukuyama-type congenital muscular dystrophy
-
Nakanishi, T., Sakauchi, M., Kaneda, Y., Tomimatsu, H., Saito, K., Nakazawa, M. and Osawa, M. (2006) Cardiac involvement in Fukuyama-type congenital muscular dystrophy. Pediatrics, 117, e1187-e1192.
-
(2006)
Pediatrics
, vol.117
-
-
Nakanishi, T.1
Sakauchi, M.2
Kaneda, Y.3
Tomimatsu, H.4
Saito, K.5
Nakazawa, M.6
Osawa, M.7
-
5
-
-
0037173670
-
Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies
-
Michele, D.E., Barresi, R., Kanagawa, M., Saito, F., Cohn, R.D., Satz, J.S., Dollar, J., Nishino, I., Kelley, R.I., Somer, H. et al. (2002) Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies. Nature, 418, 417-422.
-
(2002)
Nature
, vol.418
, pp. 417-422
-
-
Michele, D.E.1
Barresi, R.2
Kanagawa, M.3
Saito, F.4
Cohn, R.D.5
Satz, J.S.6
Dollar, J.7
Nishino, I.8
Kelley, R.I.9
Somer, H.10
-
6
-
-
43749089366
-
Gene table of monogenic neuromuscular disorders (nuclear genome only)
-
(2008) Gene table of monogenic neuromuscular disorders (nuclear genome only). Neuromuscul. Disord., 18, 101-129.
-
(2008)
Neuromuscul. Disord.
, vol.18
, pp. 101-129
-
-
-
7
-
-
3142731311
-
LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies
-
Barresi, R., Michele, D.E., Kanagawa, M., Harper, H.A., Dovico, S.A., Satz, J.S., Moore, S.A., Zhang, W., Schachter, H., Dumanski, J.P. et al. (2004) LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies. Nat. Med., 10, 696-703.
-
(2004)
Nat. Med.
, vol.10
, pp. 696-703
-
-
Barresi, R.1
Michele, D.E.2
Kanagawa, M.3
Harper, H.A.4
Dovico, S.A.5
Satz, J.S.6
Moore, S.A.7
Zhang, W.8
Schachter, H.9
Dumanski, J.P.10
-
8
-
-
2942733346
-
Molecular recognition by LARGE is essential for expression of functional dystroglycan
-
Kanagawa, M., Saito, F., Kunz, S., Yoshida-Moriguchi, T., Barresi, R., Kobayashi, Y.M., Muschler, J., Dumanski, J.P., Michele, D.E., Oldstone, M.B. et al. (2004) Molecular recognition by LARGE is essential for expression of functional dystroglycan. Cell, 117, 953-964.
-
(2004)
Cell
, vol.117
, pp. 953-964
-
-
Kanagawa, M.1
Saito, F.2
Kunz, S.3
Yoshida-Moriguchi, T.4
Barresi, R.5
Kobayashi, Y.M.6
Muschler, J.7
Dumanski, J.P.8
Michele, D.E.9
Oldstone, M.B.10
-
9
-
-
0034975777
-
Mutant glycosyltransferase and altered glycosylation of alpha-dystroglycan in the myodystrophy mouse
-
Grewal, P.K., Holzfeind, P.J., Bittner, R.E. and Hewitt, J.E. (2001) Mutant glycosyltransferase and altered glycosylation of alpha-dystroglycan in the myodystrophy mouse. Nat. Genet., 28, 151-154.
-
(2001)
Nat. Genet.
, vol.28
, pp. 151-154
-
-
Grewal, P.K.1
Holzfeind, P.J.2
Bittner, R.E.3
Hewitt, J.E.4
-
10
-
-
27244440999
-
Characterization of the LARGE family of putative glycosyltransferases associated with dystroglycanopathies
-
Grewal, P.K., McLaughlan, J.M., Moore, C.J., Browning, C.A. and Hewitt, J.E. (2005) Characterization of the LARGE family of putative glycosyltransferases associated with dystroglycanopathies. Glycobiology, 15, 912-923.
-
(2005)
Glycobiology
, vol.15
, pp. 912-923
-
-
Grewal, P.K.1
McLaughlan, J.M.2
Moore, C.J.3
Browning, C.A.4
Hewitt, J.E.5
-
11
-
-
10744226857
-
Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan
-
Longman, C., Brockington, M., Torelli, S., Jimenez-Mallebrera, C., Kennedy, C., Khalil, N., Feng, L., Saran, R.K., Voit, T., Merlini, L. et al. (2003) Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan. Hum. Mol. Genet., 12, 2853-2861.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 2853-2861
-
-
Longman, C.1
Brockington, M.2
Torelli, S.3
Jimenez-Mallebrera, C.4
Kennedy, C.5
Khalil, N.6
Feng, L.7
Saran, R.K.8
Voit, T.9
Merlini, L.10
-
12
-
-
0036799939
-
Skeletal, cardiac and tongue muscle pathology, defective retinal transmission, and neuronal migration defects in the Large(myd) mouse denes a natural model for glycosylation-decient muscle-eye-brain disorders
-
Holzfeind, P.J., Grewal, P.K., Reitsamer, H.A., Kechvar, J., Lassmann, H., Hoeger, H., Hewitt, J.E. and Bittner, R.E. (2002) Skeletal, cardiac and tongue muscle pathology, defective retinal transmission, and neuronal migration defects in the Large(myd) mouse denes a natural model for glycosylation-decient muscle-eye-brain disorders. Hum. Mol. Genet., 11, 2673-2687.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 2673-2687
-
-
Holzfeind, P.J.1
Grewal, P.K.2
Reitsamer, H.A.3
Kechvar, J.4
Lassmann, H.5
Hoeger, H.6
Hewitt, J.E.7
Bittner, R.E.8
-
13
-
-
79952391340
-
A dystroglycan mutation associated with limb-girdle muscular dystrophy
-
Hara, Y., Balci-Hayta, B., Yoshida-Moriguchi, T., Kanagawa, M., Beltran-Valero de Bernabe, D., Gundesli, H., Willer, T., Satz, J.S., Crawford, R.W., Burden, S.J. et al. (2011) A dystroglycan mutation associated with limb-girdle muscular dystrophy. N. Engl. J. Med., 364, 939-946.
-
(2011)
N. Engl. J. Med.
, vol.364
, pp. 939-946
-
-
Hara, Y.1
Balci-Hayta, B.2
Yoshida-Moriguchi, T.3
Kanagawa, M.4
Beltran-Valero de Bernabe, D.5
Gundesli, H.6
Willer, T.7
Satz, J.S.8
Crawford, R.W.9
Burden, S.J.10
-
14
-
-
0027275643
-
A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin
-
Ervasti, J.M. and Campbell, K.P. (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
-
15
-
-
0026543686
-
Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix
-
Ibraghimov-Beskrovnaya, O., Ervasti, J.M., Leveille, C.J., Slaughter, C.A., Sernett, S.W. and Campbell, K.P. (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
-
16
-
-
0035939672
-
A stoichiometric complex of neurexins and dystroglycan in brain
-
Sugita, S., Saito, F., Tang, J., Satz, J., Campbell, K. and Sudhof, T.C. (2001) A stoichiometric complex of neurexins and dystroglycan in brain. J. Cell Biol., 154, 435-445.
-
(2001)
J. Cell Biol.
, vol.154
, pp. 435-445
-
-
Sugita, S.1
Saito, F.2
Tang, J.3
Satz, J.4
Campbell, K.5
Sudhof, T.C.6
-
17
-
-
0028178082
-
Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor
-
Gee, S.H., Montanaro, F., Lindenbaum, M.H. and Carbonetto, S. (1994) Dystroglycan-alpha, 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
-
18
-
-
72449123264
-
Dystroglycan matrix receptor function in cardiac myocytes is important for limiting activity-induced myocardial damage
-
Michele, D.E., Kabaeva, Z., Davis, S.L., Weiss, R.M. and Campbell, K.P. (2009) Dystroglycan matrix receptor function in cardiac myocytes is important for limiting activity-induced myocardial damage. Circ. Res., 105, 984-993.
-
(2009)
Circ. Res.
, vol.105
, pp. 984-993
-
-
Michele, D.E.1
Kabaeva, Z.2
Davis, S.L.3
Weiss, R.M.4
Campbell, K.P.5
-
19
-
-
0025272250
-
Deciency of a glycoprotein component of the dystrophin complex in dystrophic muscle
-
Ervasti, J.M., Ohlendieck, K., Kahl, S.D., Gaver, M.G. and Campbell, K.P. (1990) Deciency of a glycoprotein component of the dystrophin complex in dystrophic muscle. Nature, 345, 315-319.
-
(1990)
Nature
, vol.345
, pp. 315-319
-
-
Ervasti, J.M.1
Ohlendieck, K.2
Kahl, S.D.3
Gaver, M.G.4
Campbell, K.P.5
-
20
-
-
0033963757
-
Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E
-
Durbeej, M., Cohn, R.D., Hrstka, R.F., Moore, S.A., Allamand, V., Davidson, B.L., Williamson, R.A. and Campbell, K.P. (2000) Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E. Mol. Cell, 5, 141-151.
-
(2000)
Mol. Cell
, vol.5
, pp. 141-151
-
-
Durbeej, M.1
Cohn, R.D.2
Hrstka, R.F.3
Moore, S.A.4
Allamand, V.5
Davidson, B.L.6
Williamson, R.A.7
Campbell, K.P.8
-
21
-
-
0030991963
-
A role of dystroglycan in schwannoma cell adhesion to laminin
-
Matsumura, K., Chiba, A., Yamada, H., Fukuta-Ohi, H., Fujita, S., Endo, T., Kobata, A., Anderson, L.V., Kanazawa, I., Campbell, K.P. et al. (1997) A role of dystroglycan in schwannoma cell adhesion to laminin. J. Biol. Chem., 272, 13904-13910.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 13904-13910
-
-
Matsumura, K.1
Chiba, A.2
Yamada, H.3
Fukuta-Ohi, H.4
Fujita, S.5
Endo, T.6
Kobata, A.7
Anderson, L.V.8
Kanazawa, I.9
Campbell, K.P.10
-
22
-
-
66449083253
-
Loss of alpha-dystroglycan laminin binding in epithelium-derived cancers is caused by silencing of LARGE
-
de Bernabe, D.B., Inamori, K., Yoshida-Moriguchi, T., Weydert, C.J., Harper, H.A., Willer, T., Henry, M.D. and Campbell, K.P. (2009) Loss of alpha-dystroglycan laminin binding in epithelium-derived cancers is caused by silencing of LARGE. J. Biol. Chem., 284, 11279-11284.
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 11279-11284
-
-
de Bernabe, D.B.1
Inamori, K.2
Yoshida-Moriguchi, T.3
Weydert, C.J.4
Harper, H.A.5
Willer, T.6
Henry, M.D.7
Campbell, K.P.8
-
23
-
-
0345505670
-
Dystroglycan expression is frequently reduced in human breast and colon cancers and is associated with tumor progression
-
Sgambato, A., Migaldi, M., Montanari, M., Camerini, A., Brancaccio, A., Rossi, G., Cangiano, R., Losasso, C., Capelli, G., Trentini, G.P. et al. (2003) Dystroglycan expression is frequently reduced in human breast and colon cancers and is associated with tumor progression. Am. J. Pathol., 162, 849-860.
-
(2003)
Am. J. Pathol.
, vol.162
, pp. 849-860
-
-
Sgambato, A.1
Migaldi, M.2
Montanari, M.3
Camerini, A.4
Brancaccio, A.5
Rossi, G.6
Cangiano, R.7
Losasso, C.8
Capelli, G.9
Trentini, G.P.10
-
24
-
-
0033519279
-
Laminin polymerization induces a receptor-cytoskeleton network
-
Colognato, H., Winkelmann, D.A. and Yurchenco, P.D. (1999) Laminin polymerization induces a receptor-cytoskeleton network. J. Cell Biol., 145, 619-631.
-
(1999)
J. Cell Biol.
, vol.145
, pp. 619-631
-
-
Colognato, H.1
Winkelmann, D.A.2
Yurchenco, P.D.3
-
25
-
-
34547093441
-
Role of laminin terminal globular domains in basement membrane assembly
-
McKee, K.K., Harrison, D., Capizzi, S. and Yurchenco, P.D. (2007) Role of laminin terminal globular domains in basement membrane assembly. J. Biol. Chem., 282, 21437-21447.
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 21437-21447
-
-
McKee, K.K.1
Harrison, D.2
Capizzi, S.3
Yurchenco, P.D.4
-
26
-
-
0032445403
-
A role for dystroglycan in basement membrane assembly
-
Henry, M.D. and Campbell, K.P. (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
-
27
-
-
0030927063
-
Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice
-
Williamson, R.A., Henry, M.D., Daniels, K.J., Hrstka, R.F., Lee, J.C., Sunada, Y., Ibraghimov-Beskrovnaya, O. and Campbell, K.P. (1997) Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice. Hum. Mol. Genet., 6, 831-841.
-
(1997)
Hum. 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
-
28
-
-
0037461292
-
The phenotype of limb-girdle muscular dystrophy type 2I
-
Poppe, M., Cree, L., Bourke, J., Eagle, M., Anderson, L.V., Birchall, D., Brockington, M., Buddles, M., Busby, M., Muntoni, F. et al. (2003) The phenotype of limb-girdle muscular dystrophy type 2I. Neurology, 60, 1246-1251.
-
(2003)
Neurology
, vol.60
, pp. 1246-1251
-
-
Poppe, M.1
Cree, L.2
Bourke, J.3
Eagle, M.4
Anderson, L.V.5
Birchall, D.6
Brockington, M.7
Buddles, M.8
Busby, M.9
Muntoni, F.10
-
29
-
-
9144248503
-
Cardiac and respiratory failure in limb-girdle muscular dystrophy 2I
-
Poppe, M., Bourke, J., Eagle, M., Frosk, P., Wrogemann, K., Greenberg, C., Muntoni, F., Voit, T., Straub, V., Hilton-Jones, D. et al. (2004) Cardiac and respiratory failure in limb-girdle muscular dystrophy 2I. Ann. Neurol., 56, 738-741.
-
(2004)
Ann. Neurol.
, vol.56
, pp. 738-741
-
-
Poppe, M.1
Bourke, J.2
Eagle, M.3
Frosk, P.4
Wrogemann, K.5
Greenberg, C.6
Muntoni, F.7
Voit, T.8
Straub, V.9
Hilton-Jones, D.10
-
30
-
-
28944454254
-
Clinical and molecular characterization of patients with limb-girdle muscular dystrophy type 2I
-
Boito, C.A., Melacini, P., Vianello, A., Prandini, P., Gavassini, B.F., Bagattin, A., Siciliano, G., Angelini, C. and Pegoraro, E. (2005) Clinical and molecular characterization of patients with limb-girdle muscular dystrophy type 2I. Arch. Neurol., 62, 1894-1899.
-
(2005)
Arch. Neurol.
, vol.62
, pp. 1894-1899
-
-
Boito, C.A.1
Melacini, P.2
Vianello, A.3
Prandini, P.4
Gavassini, B.F.5
Bagattin, A.6
Siciliano, G.7
Angelini, C.8
Pegoraro, E.9
-
31
-
-
0035212037
-
Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deciency and abnormal glycosylation of alpha-dystroglycan
-
Brockington, M., Blake, D.J., Prandini, P., Brown, S.C., Torelli, S., Benson, M.A., Ponting, C.P., Estournet, B., Romero, N.B., Mercuri, E. et al. (2001) Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deciency and abnormal glycosylation of alpha-dystroglycan. Am. J. Hum. Genet., 69, 1198-1209.
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 1198-1209
-
-
Brockington, M.1
Blake, D.J.2
Prandini, P.3
Brown, S.C.4
Torelli, S.5
Benson, M.A.6
Ponting, C.P.7
Estournet, B.8
Romero, N.B.9
Mercuri, E.10
-
32
-
-
18244375299
-
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C
-
Brockington, M., Yuva, Y., Prandini, P., Brown, S.C., Torelli, S., Benson, M.A., Herrmann, R., Anderson, L.V., Bashir, R., Burgunder, J.M. et al. (2001) Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C. Hum. Mol. Genet., 10, 2851-2859.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 2851-2859
-
-
Brockington, M.1
Yuva, Y.2
Prandini, P.3
Brown, S.C.4
Torelli, S.5
Benson, M.A.6
Herrmann, R.7
Anderson, L.V.8
Bashir, R.9
Burgunder, J.M.10
-
33
-
-
48749108191
-
Cardiac assessment of limb-girdle muscular dystrophy 2I patients: an echography, Holter ECG and magnetic resonance imaging study
-
Wahbi, K., Meune, C., Hamouda el, H., Stojkovic, T., Laforet, P., Becane, H.M., Eymard, B. and Duboc, D. (2008) Cardiac assessment of limb-girdle muscular dystrophy 2I patients: an echography, Holter ECG and magnetic resonance imaging study. Neuromuscul. Disord., 18, 650-655.
-
(2008)
Neuromuscul. Disord
, vol.18
, pp. 650-655
-
-
Wahbi, K.1
Meune, C.2
Hamouda el, H.3
Stojkovic, T.4
Laforet, P.5
Becane, H.M.6
Eymard, B.7
Duboc, D.8
-
34
-
-
39649114989
-
Heart transplantation in a child with LGMD2I presenting as isolated dilated cardiomyopathy
-
D'Amico, A., Petrini, S., Parisi, F., Tessa, A., Francalanci, P., Grutter, G., Santorelli, F.M. and Bertini, E. (2008) Heart transplantation in a child with LGMD2I presenting as isolated dilated cardiomyopathy. Neuromuscul. Disord., 18, 153-155.
-
(2008)
Neuromuscul. Disord.
, vol.18
, pp. 153-155
-
-
D'Amico, A.1
Petrini, S.2
Parisi, F.3
Tessa, A.4
Francalanci, P.5
Grutter, G.6
Santorelli, F.M.7
Bertini, E.8
-
35
-
-
33845309490
-
Fukutin gene mutations cause dilated cardiomyopathy with minimal muscle weakness
-
Murakami, T., Hayashi, Y.K., Noguchi, S., Ogawa, M., Nonaka, I., Tanabe, Y., Ogino, M., Takada, F., Eriguchi, M., Kotooka, N. et al. (2006) Fukutin gene mutations cause dilated cardiomyopathy with minimal muscle weakness. Ann. Neurol., 60, 597-602.
-
(2006)
Ann. Neurol.
, vol.60
, pp. 597-602
-
-
Murakami, T.1
Hayashi, Y.K.2
Noguchi, S.3
Ogawa, M.4
Nonaka, I.5
Tanabe, Y.6
Ogino, M.7
Takada, F.8
Eriguchi, M.9
Kotooka, N.10
-
36
-
-
77950232997
-
Use of Evans blue dye to compare limb muscles in exercised young and old mdx mice
-
Wooddell, C.I., Zhang, G., Grifn, J.B., Hegge, J.O., Huss, T. and Wolff, J.A. (2010) Use of Evans blue dye to compare limb muscles in exercised young and old mdx mice. Muscle Nerve, 41, 487-499.
-
(2010)
Muscle Nerve
, vol.41
, pp. 487-499
-
-
Wooddell, C.I.1
Zhang, G.2
Grifn, J.B.3
Hegge, J.O.4
Huss, T.5
Wolff, J.A.6
-
37
-
-
0037166935
-
Matrix assembly, regulation, and survival functions of laminin and its receptors in embryonic stem cell differentiation
-
Li, S., Harrison, D., Carbonetto, S., Fassler, R., Smyth, N., Edgar, D. and Yurchenco, P.D. (2002) Matrix assembly, regulation, and survival functions of laminin and its receptors in embryonic stem cell differentiation. J. Cell Biol., 157, 1279-1290.
-
(2002)
J. Cell Biol.
, vol.157
, pp. 1279-1290
-
-
Li, S.1
Harrison, D.2
Carbonetto, S.3
Fassler, R.4
Smyth, N.5
Edgar, D.6
Yurchenco, P.D.7
-
38
-
-
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
-
39
-
-
0033454069
-
Optimized uorescent probe combinations for evaluation of proliferation and necrosis in anthracycline-treated leukaemic cell lines
-
Boutonnat, J., Barbier, M., Muirhead, K., Mousseau, M., Ronot, X. and Seigneurin, D. (1999) Optimized uorescent probe combinations for evaluation of proliferation and necrosis in anthracycline-treated leukaemic cell lines. Cell Prolif., 32, 203-213.
-
(1999)
Cell Prolif.
, vol.32
, pp. 203-213
-
-
Boutonnat, J.1
Barbier, M.2
Muirhead, K.3
Mousseau, M.4
Ronot, X.5
Seigneurin, D.6
-
40
-
-
0021983304
-
Adhesion of cardiac myocytes to extracellular matrix components
-
Lundgren, E., Terracio, L. and Borg, T.K. (1985) Adhesion of cardiac myocytes to extracellular matrix components. Basic Res. Cardiol., 80(Suppl. 1), 69-74.
-
(1985)
Basic Res. Cardiol.
, vol.80
, Issue.SUPPL. 1
, pp. 69-74
-
-
Lundgren, E.1
Terracio, L.2
Borg, T.K.3
-
41
-
-
65649130436
-
Developmental and pathogenic mechanisms of basement membrane assembly
-
Yurchenco, P.D. and Patton, B.L. (2009) Developmental and pathogenic mechanisms of basement membrane assembly. Curr. Pharm. Des., 15, 1277-1294.
-
(2009)
Curr. Pharm. Des.
, vol.15
, pp. 1277-1294
-
-
Yurchenco, P.D.1
Patton, B.L.2
-
42
-
-
33744784550
-
Alpha7beta1-integrin regulates mechanotransduction and prevents skeletal muscle injury
-
Boppart, M.D., Burkin, D.J. and Kaufman, S.J. (2006) Alpha7beta1-integrin regulates mechanotransduction and prevents skeletal muscle injury. Am. J. Physiol. Cell Physiol., 290, C1660-C1665.
-
(2006)
Am. J. Physiol. Cell Physiol.
, vol.290
-
-
Boppart, M.D.1
Burkin, D.J.2
Kaufman, S.J.3
-
43
-
-
0035911960
-
Enhanced expression of the alpha 7 beta 1 integrin reduces muscular dystrophy and restores viability in dystrophic mice
-
Burkin, D.J., Wallace, G.Q., Nicol, K.J., Kaufman, D.J. and Kaufman, S.J. (2001) Enhanced expression of the alpha 7 beta 1 integrin reduces muscular dystrophy and restores viability in dystrophic mice. J. Cell Biol., 152, 1207-1218.
-
(2001)
J. Cell Biol.
, vol.152
, pp. 1207-1218
-
-
Burkin, D.J.1
Wallace, G.Q.2
Nicol, K.J.3
Kaufman, D.J.4
Kaufman, S.J.5
-
44
-
-
0033605651
-
Activation of the Cdc42-associated tyrosine kinase-2 (ACK-2) by cell adhesion via integrin beta1
-
Yang, W., Lin, Q., Guan, J.L. and Cerione, R.A. (1999) Activation of the Cdc42-associated tyrosine kinase-2 (ACK-2) by cell adhesion via integrin beta1. J. Biol. Chem., 274, 8524-8530.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 8524-8530
-
-
Yang, W.1
Lin, Q.2
Guan, J.L.3
Cerione, R.A.4
-
45
-
-
0037832412
-
The basement membrane/basal lamina of skeletal muscle
-
Sanes, J.R. (2003) The basement membrane/basal lamina of skeletal muscle. J. Biol. Chem., 278, 12601-12604.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 12601-12604
-
-
Sanes, J.R.1
-
46
-
-
0027360897
-
Abnormal localization of laminin subunits in muscular dystrophies
-
Hayashi, Y.K., Engvall, E., Arikawa-Hirasawa, E., Goto, K., Koga, R., Nonaka, I., Sugita, H. and Arahata, K. (1993) Abnormal localization of laminin subunits in muscular dystrophies. J. Neurol. Sci., 119, 53-64.
-
(1993)
J. Neurol. Sci.
, vol.119
, pp. 53-64
-
-
Hayashi, Y.K.1
Engvall, E.2
Arikawa-Hirasawa, E.3
Goto, K.4
Koga, R.5
Nonaka, I.6
Sugita, H.7
Arahata, K.8
-
47
-
-
0034605070
-
The dystrophin complex forms a mechanically strong link between the sarcolemma and costameric actin
-
Rybakova, I.N., Patel, J.R. and Ervasti, J.M. (2000) The dystrophin complex forms a mechanically strong link between the sarcolemma and costameric actin. J. Cell Biol., 150, 1209-1214.
-
(2000)
J. Cell Biol.
, vol.150
, pp. 1209-1214
-
-
Rybakova, I.N.1
Patel, J.R.2
Ervasti, J.M.3
-
48
-
-
0038190993
-
Costameres: the Achilles' heel of Herculean muscle
-
Ervasti, J.M. (2003) Costameres: the Achilles' heel of Herculean muscle. J. Biol. Chem., 278, 13591-13594.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 13591-13594
-
-
Ervasti, J.M.1
-
49
-
-
79951974764
-
Lateral transmission of force is impaired in skeletal muscles of dystrophic mice and very old rats
-
Ramaswamy, K.S., Palmer, M.L., van der Meulen, J.H., Renoux, A., Kostrominova, T.Y., Michele, D.E. and Faulkner, J.A. (2011) Lateral transmission of force is impaired in skeletal muscles of dystrophic mice and very old rats. J. Physiol., 589, 1195-1208.
-
(2011)
J. Physiol.
, vol.589
, pp. 1195-1208
-
-
Ramaswamy, K.S.1
Palmer, M.L.2
van der Meulen, J.H.3
Renoux, A.4
Kostrominova, T.Y.5
Michele, D.E.6
Faulkner, J.A.7
-
50
-
-
0030783172
-
Animal models for muscular dystrophy show different patterns of sarcolemmal disruption
-
Straub, V., Rafael, J.A., Chamberlain, J.S. and Campbell, K.P. (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
-
51
-
-
0035494438
-
A nitric oxide synthase transgene ameliorates muscular dystrophy in mdx mice
-
Wehling, M., Spencer, M.J. and Tidball, J.G. (2001) A nitric oxide synthase transgene ameliorates muscular dystrophy in mdx mice. J. Cell Biol., 155, 123-131.
-
(2001)
J. Cell Biol.
, vol.155
, pp. 123-131
-
-
Wehling, M.1
Spencer, M.J.2
Tidball, J.G.3
-
52
-
-
0035975968
-
Muscular degeneration in the absence of dystrophin is a calcium-dependent process
-
Mariol, M.C. and Segalat, L. (2001) Muscular degeneration in the absence of dystrophin is a calcium-dependent process. Curr. Biol., 11, 1691-1694.
-
(2001)
Curr. Biol.
, vol.11
, pp. 1691-1694
-
-
Mariol, M.C.1
Segalat, L.2
-
53
-
-
0033588050
-
Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy
-
Coral-Vazquez, R., Cohn, R.D., Moore, S.A., Hill, J.A., Weiss, R.M., Davisson, R.L., Straub, V., Barresi, R., Bansal, D., Hrstka, R.F. et al. (1999) Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy. Cell, 98, 465-474.
-
(1999)
Cell
, vol.98
, pp. 465-474
-
-
Coral-Vazquez, R.1
Cohn, R.D.2
Moore, S.A.3
Hill, J.A.4
Weiss, R.M.5
Davisson, R.L.6
Straub, V.7
Barresi, R.8
Bansal, D.9
Hrstka, R.F.10
-
54
-
-
23944459786
-
Dystrophic heart failure blocked by membrane sealant poloxamer
-
Yasuda, S., Townsend, D., Michele, D.E., Favre, E.G., Day, S.M. and Metzger, J.M. (2005) Dystrophic heart failure blocked by membrane sealant poloxamer. Nature, 436, 1025-1029.
-
(2005)
Nature
, vol.436
, pp. 1025-1029
-
-
Yasuda, S.1
Townsend, D.2
Michele, D.E.3
Favre, E.G.4
Day, S.M.5
Metzger, J.M.6
-
55
-
-
78751682676
-
Interleukin-10 reduces the pathology of mdx muscular dystrophy by deactivating M1 macrophages and modulating macrophage phenotype
-
Villalta, S.A., Rinaldi, C., Deng, B., Liu, G., Fedor, B. and Tidball, J.G. (2011) Interleukin-10 reduces the pathology of mdx muscular dystrophy by deactivating M1 macrophages and modulating macrophage phenotype. Hum. Mol. Genet., 20, 790-805.
-
(2011)
Hum. Mol. Genet.
, vol.20
, pp. 790-805
-
-
Villalta, S.A.1
Rinaldi, C.2
Deng, B.3
Liu, G.4
Fedor, B.5
Tidball, J.G.6
-
56
-
-
79951479823
-
Losartan decreases cardiac muscle brosis and improves cardiac function in dystrophin-decient mdx mice
-
Spurney, C.F., Sali, A., Guerron, A.D., Iantorno, M., Yu, Q., Gordish-Dressman, H., Rayavarapu, S., van der Meulen, J., Hoffman, E.P. and Nagaraju, K. (2011) Losartan decreases cardiac muscle brosis and improves cardiac function in dystrophin-decient mdx mice. J. Cardiovasc. Pharmacol. Ther., 16, 87-95.
-
(2011)
J. Cardiovasc. Pharmacol. Ther.
, vol.16
, pp. 87-95
-
-
Spurney, C.F.1
Sali, A.2
Guerron, A.D.3
Iantorno, M.4
Yu, Q.5
Gordish-Dressman, H.6
Rayavarapu, S.7
van der Meulen, J.8
Hoffman, E.P.9
Nagaraju, K.10
-
57
-
-
0003633755
-
-
Institute for Laboratory Animal Research National Research Council. National Academy Press, Washington, DC
-
Institute for Laboratory Animal Research. National Research Council. (1996) Guide for the care and use of laboratory animals. National Academy Press, Washington, DC.
-
(1996)
Guide for the care and use of laboratory animals
-
-
-
58
-
-
41749095167
-
Blebbistatin extends culture life of adult mouse cardiac myocytes and allows efcient and stable transgene expression
-
Kabaeva, Z., Zhao, M. and Michele, D.E. (2008) Blebbistatin extends culture life of adult mouse cardiac myocytes and allows efcient and stable transgene expression. Am. J. Physiol. Heart Circ. Physiol., 294, H1667-H1674.
-
(2008)
Am. J. Physiol. Heart Circ. Physiol.
, vol.294
-
-
Kabaeva, Z.1
Zhao, M.2
Michele, D.E.3
|