-
1
-
-
79957622998
-
Dystroglycanopathies: coming into focus
-
Godfrey, C., Foley, A.R., Clement, E. and Muntoni, F. (2011) Dystroglycanopathies: coming into focus. Curr. Opin. Genet. Dev., 21, 278-285.
-
(2011)
Curr. Opin. Genet. Dev.
, vol.21
, pp. 278-285
-
-
Godfrey, C.1
Foley, A.R.2
Clement, E.3
Muntoni, F.4
-
2
-
-
0035838362
-
Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy
-
Hayashi, Y.K., Ogawa, M., Tagawa, K., Noguchi, S., Ishihara, T., Nonaka, I. and Arahata, K. (2001) Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy. Neurology, 57, 115-121.
-
(2001)
Neurology
, vol.57
, pp. 115-121
-
-
Hayashi, Y.K.1
Ogawa, M.2
Tagawa, K.3
Noguchi, S.4
Ishihara, T.5
Nonaka, I.6
Arahata, K.7
-
3
-
-
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
-
4
-
-
0032560851
-
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy
-
Kobayashi, K., Nakahori, Y., Miyake, M., Matsumura, K., Kondo-Iida, E., Nomura, Y., Segawa, M., Yoshioka, M., Saito, K., Osawa, M. et al. (1998) An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy. Nature, 394, 388-392.
-
(1998)
Nature
, vol.394
, pp. 388-392
-
-
Kobayashi, K.1
Nakahori, Y.2
Miyake, M.3
Matsumura, K.4
Kondo-Iida, E.5
Nomura, Y.6
Segawa, M.7
Yoshioka, M.8
Saito, K.9
Osawa, M.10
-
5
-
-
80053898946
-
Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy
-
Taniguchi-Ikeda, M., Kobayashi, K., Kanagawa, M., Yu, C.C., Mori, K., Oda, T., Kuga, A., Kurahashi, H., Akman, H.O., DiMauro, S. et al. (2011) Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy. Nature, 478, 127-131.
-
(2011)
Nature
, vol.478
, pp. 127-131
-
-
Taniguchi-Ikeda, M.1
Kobayashi, K.2
Kanagawa, M.3
Yu, C.C.4
Mori, K.5
Oda, T.6
Kuga, A.7
Kurahashi, H.8
Akman, H.O.9
DiMauro, S.10
-
6
-
-
0019471880
-
Congenital progressive muscular dystrophy of the Fukuyama type-clinical, genetic and pathological considerations
-
Fukuyama, Y., Osawa, M. and Suzuki, H. (1981) Congenital progressive muscular dystrophy of the Fukuyama type-clinical, genetic and pathological considerations. Brain Dev., 3, 1-29.
-
(1981)
Brain Dev.
, vol.3
, pp. 1-29
-
-
Fukuyama, Y.1
Osawa, M.2
Suzuki, H.3
-
7
-
-
34848837334
-
Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan
-
Godfrey, C., Clement, E., Mein, R., Brockington, M., Smith, J., Talim, B., Straub, V., Robb, S., Quinlivan, R., Feng, L. et al. (2007) Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan. Brain, 130, 2725-2735.
-
(2007)
Brain
, vol.130
, pp. 2725-2735
-
-
Godfrey, C.1
Clement, E.2
Mein, R.3
Brockington, M.4
Smith, J.5
Talim, B.6
Straub, V.7
Robb, S.8
Quinlivan, R.9
Feng, L.10
-
8
-
-
84858061102
-
Mislocalization of fukutin protein by disease-causing missense mutations can be rescued with treatments directed at folding amelioration
-
Tachikawa, M., Kanagawa, M., Yu, C.C., Kobayashi, K. and Toda, T. (2012) Mislocalization of fukutin protein by disease-causing missense mutations can be rescued with treatments directed at folding amelioration. J. Biol. Chem., 287, 8398-8406.
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 8398-8406
-
-
Tachikawa, M.1
Kanagawa, M.2
Yu, C.C.3
Kobayashi, K.4
Toda, T.5
-
9
-
-
84874883376
-
The O-mannosylation pathway: glycosyltransferases and proteins implicated in congenital muscular dystrophy
-
Wells, L. (2013) The O-mannosylation pathway: glycosyltransferases and proteins implicated in congenital muscular dystrophy. J. Biol. Chem., 288, 6930-6935.
-
(2013)
J. Biol. Chem.
, vol.288
, pp. 6930-6935
-
-
Wells, L.1
-
10
-
-
84875953109
-
Missense mutations in b-1,3-Nacetylglucosaminyltransferase 1 (B3GNT1) cause Walker-Warburg syndrome
-
Buysse, K., Riemersma, M., Powell, G., van Reeuwijk, J., Chitayat, D., Roscioli, T., Kamsteeg, E.J., van den Elzen, C., van Beusekom, E., Blaser, S. et al. (2013) Missense mutations in b-1,3-Nacetylglucosaminyltransferase 1 (B3GNT1) cause Walker-Warburg syndrome. Hum. Mol. Genet., 22, 1746-1754.
-
(2013)
Hum. Mol. Genet.
, vol.22
, pp. 1746-1754
-
-
Buysse, K.1
Riemersma, M.2
Powell, G.3
van Reeuwijk, J.4
Chitayat, D.5
Roscioli, T.6
Kamsteeg, E.J.7
van den Elzen, C.8
van Beusekom, E.9
Blaser, S.10
-
11
-
-
0347635516
-
Demonstration of mammalian protein O-mannosyltransferase activity: coexpression of POMT1 and POMT2 required for enzymatic activity
-
Manya, H., Chiba, A., Yoshida, A., Wang, X., Chiba, Y., Jigami, Y., Margolis, R.U. and Endo, T. (2004) Demonstration of mammalian protein O-mannosyltransferase activity: coexpression of POMT1 and POMT2 required for enzymatic activity. Proc. Natl Acad. Sci. USA, 101, 500-505.
-
(2004)
Proc. Natl Acad. Sci. USA
, vol.101
, pp. 500-505
-
-
Manya, H.1
Chiba, A.2
Yoshida, A.3
Wang, X.4
Chiba, Y.5
Jigami, Y.6
Margolis, R.U.7
Endo, T.8
-
12
-
-
18044400450
-
Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1
-
Yoshida, A., Kobayashi, K., Manya, H., Taniguchi, K., Kano, H., Mizuno, M., Inazu, T., Mitsuhashi, H., Takahashi, S., Takeuchi, M. et al. (2001) Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1. Dev. Cell, 1, 717-724.
-
(2001)
Dev. Cell
, vol.1
, pp. 717-724
-
-
Yoshida, A.1
Kobayashi, K.2
Manya, H.3
Taniguchi, K.4
Kano, H.5
Mizuno, M.6
Inazu, T.7
Mitsuhashi, H.8
Takahashi, S.9
Takeuchi, M.10
-
13
-
-
74849131820
-
O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding
-
Yoshida-Moriguchi, T., Yu, L., Stalnaker, S.H., Davis, S., Kunz, S., Madson, M., Oldstone, M.B., Schachter, H., Wells, L. and Campbell, K.P. (2010) O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding. Science, 327, 88-92.
-
(2010)
Science
, vol.327
, pp. 88-92
-
-
Yoshida-Moriguchi, T.1
Yu, L.2
Stalnaker, S.H.3
Davis, S.4
Kunz, S.5
Madson, M.6
Oldstone, M.B.7
Schachter, H.8
Wells, L.9
Campbell, K.P.10
-
14
-
-
84858598482
-
Absence of post-phosphoryl modification in dystroglycanopathy mouse models and wild-type tissues expressing non-laminin binding form of a-dystroglycan
-
Kuga, A., Kanagawa, M., Sudo, A., Chan, Y.M., Tajiri, M., Manya, H., Kikkawa, Y., Nomizu, M., Kobayashi, K., Endo, T. et al. (2012) Absence of post-phosphoryl modification in dystroglycanopathy mouse models and wild-type tissues expressing non-laminin binding form of a-dystroglycan. J. Biol. Chem., 287, 9560-9567.
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 9560-9567
-
-
Kuga, A.1
Kanagawa, M.2
Sudo, A.3
Chan, Y.M.4
Tajiri, M.5
Manya, H.6
Kikkawa, Y.7
Nomizu, M.8
Kobayashi, K.9
Endo, T.10
-
15
-
-
84855515852
-
Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE
-
Inamori, K., Yoshida-Moriguchi, T., Hara, Y., Anderson, M.E., Yu, L. and Campbell, K.P. (2012) Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE. Science, 335, 93-96.
-
(2012)
Science
, vol.335
, pp. 93-96
-
-
Inamori, K.1
Yoshida-Moriguchi, T.2
Hara, Y.3
Anderson, M.E.4
Yu, L.5
Campbell, K.P.6
-
16
-
-
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
-
17
-
-
32244440192
-
Dystroglycan: from biosynthesis to pathogenesis of human disease
-
Barresi, R. and Campbell, K.P. (2006) Dystroglycan: from biosynthesis to pathogenesis of human disease. J. Cell Sci., 119, 199-207.
-
(2006)
J. Cell Sci.
, vol.119
, pp. 199-207
-
-
Barresi, R.1
Campbell, K.P.2
-
18
-
-
33645806539
-
Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in alpha-dystroglycanopathies
-
Taniguchi, M., Kurahashi, H., Noguchi, S., Fukudome, T., Okinaga, T., Tsukahara, T., Tajima, Y., Ozono, K., Nishino, I., Nonaka, I. and Toda, T. (2006) Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in alpha-dystroglycanopathies. Hum. Mol. Genet., 15, 1279-1289.
-
(2006)
Hum. Mol. Genet.
, vol.15
, pp. 1279-1289
-
-
Taniguchi, M.1
Kurahashi, H.2
Noguchi, S.3
Fukudome, T.4
Okinaga, T.5
Tsukahara, T.6
Tajima, Y.7
Ozono, K.8
Nishino, I.9
Nonaka, I.10
Toda, T.11
-
19
-
-
79952391340
-
A dystroglycan mutation associated with limb-girdle muscular dystrophy
-
Hara, Y., Balci-Hayta, B., Yoshida-Moriguchi, T., Kanagawa, M., Beltrán-Valero de Bernabé, D., Gündeşli, 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
Beltrán-Valero de Bernabé, D.5
Gündeşli, H.6
Willer, T.7
Satz, J.S.8
Crawford, R.W.9
Burden, S.J.10
-
20
-
-
84860322514
-
Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of a-dystroglycan
-
Roscioli, T., Kamsteeg, E.J., Buysse, K., Maystadt, I., van Reeuwijk, J., van den Elzen, C., van Beusekom, E., Riemersma, M., Pfundt, R., Vissers, L.E. et al. (2012) Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of a-dystroglycan. Nat. Genet., 44, 581-585.
-
(2012)
Nat. Genet.
, vol.44
, pp. 581-585
-
-
Roscioli, T.1
Kamsteeg, E.J.2
Buysse, K.3
Maystadt, I.4
van Reeuwijk, J.5
van den Elzen, C.6
van Beusekom, E.7
Riemersma, M.8
Pfundt, R.9
Vissers, L.E.10
-
21
-
-
84860348118
-
ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome
-
Willer, T., Lee, H., Lommel, M., Yoshida-Moriguchi, T., de Bernabe, D.B., Venzke, D., Cirak, S., Schachter, H., Vajsar, J., Voit, T. et al. (2012) ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome. Nat. Genet., 44, 575-580.
-
(2012)
Nat. Genet.
, vol.44
, pp. 575-580
-
-
Willer, T.1
Lee, H.2
Lommel, M.3
Yoshida-Moriguchi, T.4
de Bernabe, D.B.5
Venzke, D.6
Cirak, S.7
Schachter, H.8
Vajsar, J.9
Voit, T.10
-
22
-
-
0032214652
-
A muscle-specific insulin receptor knockout exhibits features of the metabolic syndrome of NIDDM without altering glucose tolerance
-
Brüning, J.C., Michael, M.D., Winnay, J.N., Hayashi, T., Hörsch, D., Accili, D., Goodyear, L.J. and Kahn, C.R. (1998) A muscle-specific insulin receptor knockout exhibits features of the metabolic syndrome of NIDDM without altering glucose tolerance. Mol. Cell, 2, 559-569.
-
(1998)
Mol. Cell
, vol.2
, pp. 559-569
-
-
Brüning, J.C.1
Michael, M.D.2
Winnay, J.N.3
Hayashi, T.4
Hörsch, D.5
Accili, D.6
Goodyear, L.J.7
Kahn, C.R.8
-
23
-
-
0034535222
-
Early myotome specification regulates PDGFA expression and axial skeleton development
-
Tallquist, M.D., Weismann, K.E., Hellström, M. and Soriano, P. (2000) Early myotome specification regulates PDGFA expression and axial skeleton development. Development, 127, 5059-5070.
-
(2000)
Development
, vol.127
, pp. 5059-5070
-
-
Tallquist, M.D.1
Weismann, K.E.2
Hellström, M.3
Soriano, P.4
-
24
-
-
0026052173
-
Developmental regulation of creatine kinase gene expression by myogenic factors in embryonic mouse and chick skeletal muscle
-
Lyons, G.E., Mühlebach, S., Moser, A., Masood, R., Paterson, B.M., Buckingham, M.E. and Perriard, J.C. (1991) Developmental regulation of creatine kinase gene expression by myogenic factors in embryonic mouse and chick skeletal muscle. Development, 113, 1017-1029.
-
(1991)
Development
, vol.113
, pp. 1017-1029
-
-
Lyons, G.E.1
Mühlebach, S.2
Moser, A.3
Masood, R.4
Paterson, B.M.5
Buckingham, M.E.6
Perriard, J.C.7
-
25
-
-
0025297082
-
Tissue-specific distribution and developmental regulation of M and B creatine kinase mRNAs
-
Trask, R.V. and Billadello, J.J. (1990) Tissue-specific distribution and developmental regulation of M and B creatine kinase mRNAs. Biochim. Biophys. Acta, 1049, 182-188.
-
(1990)
Biochim. Biophys. Acta
, vol.1049
, pp. 182-188
-
-
Trask, R.V.1
Billadello, J.J.2
-
26
-
-
0031924679
-
Evidence of mdx mouse skeletal muscle fragility in vivo by eccentric running exercise
-
Vilquin, J.T., Brussee, V., Asselin, I., Kinoshita, I., Gingras, M. and Tremblay, J.P. (1998) Evidence of mdx mouse skeletal muscle fragility in vivo by eccentric running exercise. Muscle Nerve, 21, 567-576.
-
(1998)
Muscle Nerve
, vol.21
, pp. 567-576
-
-
Vilquin, J.T.1
Brussee, V.2
Asselin, I.3
Kinoshita, I.4
Gingras, M.5
Tremblay, J.P.6
-
27
-
-
0041806537
-
Gene transfer establishes primacy of striated vs. smooth muscle sarcoglycan complex in limb-girdle muscular dystrophy
-
Durbeej, M., Sawatzki, S.M., Barresi, R., Schmainda, K.M., Allamand, V., Michele, D.E. and Campbell, K.P. (2003) Gene transfer establishes primacy of striated vs. smooth muscle sarcoglycan complex in limb-girdle muscular dystrophy. Proc. Natl Acad. Sci. USA, 100, 8910-8915.
-
(2003)
Proc. Natl Acad. Sci. USA
, vol.100
, pp. 8910-8915
-
-
Durbeej, M.1
Sawatzki, S.M.2
Barresi, R.3
Schmainda, K.M.4
Allamand, V.5
Michele, D.E.6
Campbell, K.P.7
-
28
-
-
2442421775
-
Purification and cell-surface marker characterization of quiescent satellite cells from murine skeletal muscle by a novel monoclonal antibody
-
Fukada, S., Higuchi, S., Segawa, M., Koda, K., Yamamoto, Y., Tsujikawa, K., Kohama, Y., Uezumi, A., Imamura, M., Miyagoe-Suzuki, Y. et al. (2004) Purification and cell-surface marker characterization of quiescent satellite cells from murine skeletal muscle by a novel monoclonal antibody. Exp. Cell Res., 296, 245-255.
-
(2004)
Exp. Cell Res.
, vol.296
, pp. 245-255
-
-
Fukada, S.1
Higuchi, S.2
Segawa, M.3
Koda, K.4
Yamamoto, Y.5
Tsujikawa, K.6
Kohama, Y.7
Uezumi, A.8
Imamura, M.9
Miyagoe-Suzuki, Y.10
-
29
-
-
58949104792
-
Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy
-
Kanagawa, M., Nishimoto, A., Chiyonobu, T., Takeda, S., Miyagoe-Suzuki, Y., Wang, F., Fujikake, N., Taniguchi, M., Lu, Z., Tachikawa, M. et al. (2009) Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy. Hum. Mol. Genet., 18, 621-631.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 621-631
-
-
Kanagawa, M.1
Nishimoto, A.2
Chiyonobu, T.3
Takeda, S.4
Miyagoe-Suzuki, Y.5
Wang, F.6
Fujikake, N.7
Taniguchi, M.8
Lu, Z.9
Tachikawa, M.10
-
30
-
-
84865975467
-
Mouse fukutin deletion impairs dystroglycan processing and recapitulates muscular dystrophy
-
Beedle, A.M., Turner, A.J., Saito, Y., Lueck, J.D., Foltz, S.J., Fortunato, M.J., Nienaber, P.M. and Campbell, K.P. (2012) Mouse fukutin deletion impairs dystroglycan processing and recapitulates muscular dystrophy. J. Clin. Invest., 122, 3330-3342.
-
(2012)
J. Clin. Invest.
, vol.122
, pp. 3330-3342
-
-
Beedle, A.M.1
Turner, A.J.2
Saito, Y.3
Lueck, J.D.4
Foltz, S.J.5
Fortunato, M.J.6
Nienaber, P.M.7
Campbell, K.P.8
-
31
-
-
18644362893
-
Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration
-
Cohn, R.D., Henry, M.D., Michele, D.E., Barresi, R., Saito, F., Moore, S.A., Flanagan, J.D., Skwarchuk, M.W., Robbins, M.E., Mendell, J.R., Williamson, R.A. and Campbell, K.P. (2002) Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration. Cell, 110, 639-648.
-
(2002)
Cell
, vol.110
, pp. 639-648
-
-
Cohn, R.D.1
Henry, M.D.2
Michele, D.E.3
Barresi, R.4
Saito, F.5
Moore, S.A.6
Flanagan, J.D.7
Skwarchuk, M.W.8
Robbins, M.E.9
Mendell, J.R.10
Williamson, R.A.11
Campbell, K.P.12
-
32
-
-
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
-
33
-
-
80054820808
-
Like-acetylglucosaminyltransferase (LARGE)-dependent modification of dystroglycan at Thr-317/319 is required for laminin binding and arenavirus infection
-
Hara, Y., Kanagawa, M., Kunz, S., Yoshida-Moriguchi, T., Satz, J.S., Kobayashi, Y.M., Zhu, Z., Burden, S.J., Oldstone, M.B. and Campbell, K.P. (2011) Like-acetylglucosaminyltransferase (LARGE)-dependent modification of dystroglycan at Thr-317/319 is required for laminin binding and arenavirus infection. Proc. Natl Acad. Sci. USA, 108, 17426-17431.
-
(2011)
Proc. Natl Acad. Sci. USA
, vol.108
, pp. 17426-17431
-
-
Hara, Y.1
Kanagawa, M.2
Kunz, S.3
Yoshida-Moriguchi, T.4
Satz, J.S.5
Kobayashi, Y.M.6
Zhu, Z.7
Burden, S.J.8
Oldstone, M.B.9
Campbell, K.P.10
-
35
-
-
0036842214
-
Inhibition of dystroglycan binding to laminin disrupts the PI3K/AKT pathway and survival signaling in muscle cells
-
Langenbach, K.J. and Rando, T.A. (2002) Inhibition of dystroglycan binding to laminin disrupts the PI3K/AKT pathway and survival signaling in muscle cells. Muscle Nerve, 26, 644-653.
-
(2002)
Muscle Nerve
, vol.26
, pp. 644-653
-
-
Langenbach, K.J.1
Rando, T.A.2
-
36
-
-
73949151885
-
LG4-5 domains of laminin-211 binds alpha-dystroglycan to allow myotube attachment and prevent anoikis
-
Munoz, J., Zhou, Y. and Jarrett, H.W. (2010) LG4-5 domains of laminin-211 binds alpha-dystroglycan to allow myotube attachment and prevent anoikis. J. Cell. Physiol., 222, 111-119.
-
(2010)
J. Cell. Physiol.
, vol.222
, pp. 111-119
-
-
Munoz, J.1
Zhou, Y.2
Jarrett, H.W.3
-
37
-
-
77957665581
-
Direct effects of the pathogenic mutation on satellite cell function in muscular dystrophy
-
Morgan, J.E. and Zammit, P.S. (2010) Direct effects of the pathogenic mutation on satellite cell function in muscular dystrophy. Exp. Cell Res., 316, 3100-3108.
-
(2010)
Exp. Cell Res.
, vol.316
, pp. 3100-3108
-
-
Morgan, J.E.1
Zammit, P.S.2
-
38
-
-
84866663454
-
Defects in glycosylation impair satellite stem cell function and niche composition in the muscles of the dystrophic Large(myd) mouse
-
doi: 10.1002/stem.1197
-
Ross, J., Benn, A., Jonuschies, J., Boldrin, L., Muntoni, F., Hewitt, J.E., Brown, S.C. and Morgan, J.E. (2012) Defects in glycosylation impair satellite stem cell function and niche composition in the muscles of the dystrophic Large(myd) mouse. Stem Cells, doi: 10.1002/stem.1197.
-
(2012)
Stem Cells
-
-
Ross, J.1
Benn, A.2
Jonuschies, J.3
Boldrin, L.4
Muntoni, F.5
Hewitt, J.E.6
Brown, S.C.7
Morgan, J.E.8
-
39
-
-
78650432352
-
Short telomeres and stem cell exhaustion model Duchenne muscular dystrophy in mdx/mTR mice
-
Sacco, A., Mourkioti, F., Tran, R., Choi, J., Llewellyn, M., Kraft, P., Shkreli, M., Delp, S., Pomerantz, J.H., Artandi, S.E. and Blau, H.M. (2010) Short telomeres and stem cell exhaustion model Duchenne muscular dystrophy in mdx/mTR mice. Cell, 143, 1059-1071.
-
(2010)
Cell
, vol.143
, pp. 1059-1071
-
-
Sacco, A.1
Mourkioti, F.2
Tran, R.3
Choi, J.4
Llewellyn, M.5
Kraft, P.6
Shkreli, M.7
Delp, S.8
Pomerantz, J.H.9
Artandi, S.E.10
Blau, H.M.11
-
40
-
-
46049112441
-
Different autonomous myogenic cell populations revealed by ablation of Myf5-expressing cells during mouse embryogenesis
-
Gensch, N., Borchardt, T., Schneider, A., Riethmacher, D. and Braun, T. (2008) Different autonomous myogenic cell populations revealed by ablation of Myf5-expressing cells during mouse embryogenesis. Development, 135, 1597-1604.
-
(2008)
Development
, vol.135
, pp. 1597-1604
-
-
Gensch, N.1
Borchardt, T.2
Schneider, A.3
Riethmacher, D.4
Braun, T.5
-
41
-
-
33745894322
-
RAAV6-Microdystrophin preserves muscle function and extends lifespan in severely dystrophic mice
-
Gregorevic, P., Allen, J.M., Minami, E., Blankinship, M.J., Haraguchi, M., Meuse, L., Finn, E., Adams, M.E., Froehner, S.C., Murry, C.E. and Chamberlain, J.S. (2006) rAAV6-Microdystrophin preserves muscle function and extends lifespan in severely dystrophic mice. Nat. Med., 12, 787-789.
-
(2006)
Nat. Med.
, vol.12
, pp. 787-789
-
-
Gregorevic, P.1
Allen, J.M.2
Minami, E.3
Blankinship, M.J.4
Haraguchi, M.5
Meuse, L.6
Finn, E.7
Adams, M.E.8
Froehner, S.C.9
Murry, C.E.10
Chamberlain, J.S.11
-
42
-
-
7044253593
-
AAV vector-mediated microdystrophin expression in a relatively small percentage of mdx myofibers improved the mdx phenotype
-
Yoshimura, M., Sakamoto, M., Ikemoto, M., Mochizuki, Y., Yuasa, K., Miyagoe-Suzuki, Y. and Takeda, S. (2004) AAV vector-mediated microdystrophin expression in a relatively small percentage of mdx myofibers improved the mdx phenotype. Mol. Ther., 10, 821-828.
-
(2004)
Mol. Ther.
, vol.10
, pp. 821-828
-
-
Yoshimura, M.1
Sakamoto, M.2
Ikemoto, M.3
Mochizuki, Y.4
Yuasa, K.5
Miyagoe-Suzuki, Y.6
Takeda, S.7
-
43
-
-
34548784361
-
Long-term skeletal muscle protection after gene transfer in a mouse model of LGMD-2D
-
Pacak, C.A., Walter, G.A., Gaidosh, G., Bryant, N., Lewis, M.A., Germain, S., Mah, C.S., Campbell, K.P. and Byrne, B.J. (2007) Long-term skeletal muscle protection after gene transfer in a mouse model of LGMD-2D. Mol. Ther., 15, 1775-1781.
-
(2007)
Mol. Ther.
, vol.15
, pp. 1775-1781
-
-
Pacak, C.A.1
Walter, G.A.2
Gaidosh, G.3
Bryant, N.4
Lewis, M.A.5
Germain, S.6
Mah, C.S.7
Campbell, K.P.8
Byrne, B.J.9
-
44
-
-
84855161388
-
Adenovirus-associated virus vector-mediated gene transfer in hemophilia B
-
Nathwani, A.C., Tuddenham, E.G., Rangarajan, S., Rosales, C., McIntosh, J., Linch, D.C., Chowdary, P., Riddell, A., Pie, A.J., Harrington, C. et al. (2011) Adenovirus-associated virus vector-mediated gene transfer in hemophilia B. N. Engl. J. Med., 365, 2357-2365.
-
(2011)
N. Engl. J. Med.
, vol.365
, pp. 2357-2365
-
-
Nathwani, A.C.1
Tuddenham, E.G.2
Rangarajan, S.3
Rosales, C.4
McIntosh, J.5
Linch, D.C.6
Chowdary, P.7
Riddell, A.8
Pie, A.J.9
Harrington, C.10
-
45
-
-
84863878721
-
Respiratory and cardiac function in congenital muscular dystrophies with alpha dystroglycan deficiency
-
Pane, M., Messina, S., Vasco, G., Foley, A.R., Morandi, L., Pegoraro, E., Mongini, T., D'Amico, A., Bianco, F., Lombardo, M.E. et al. (2012) Respiratory and cardiac function in congenital muscular dystrophies with alpha dystroglycan deficiency. Neuromuscul. Disord., 22, 685-689.
-
(2012)
Neuromuscul. Disord.
, vol.22
, pp. 685-689
-
-
Pane, M.1
Messina, S.2
Vasco, G.3
Foley, A.R.4
Morandi, L.5
Pegoraro, E.6
Mongini, T.7
D'Amico, A.8
Bianco, F.9
Lombardo, M.E.10
-
46
-
-
77957810262
-
Post-translational maturation of dystroglycan is necessary for pikachurin binding and ribbon synaptic localization
-
Kanagawa, M., Omori, Y., Sato, S., Kobayashi, K., Miyagoe-Suzuki, Y., Takeda, S., Endo, T., Furukawa, T. and Toda, T. (2010) Post-translational maturation of dystroglycan is necessary for pikachurin binding and ribbon synaptic localization. J. Biol. Chem., 285, 31208-31216.
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 31208-31216
-
-
Kanagawa, M.1
Omori, Y.2
Sato, S.3
Kobayashi, K.4
Miyagoe-Suzuki, Y.5
Takeda, S.6
Endo, T.7
Furukawa, T.8
Toda, T.9
-
47
-
-
80053977519
-
Hesr1 and Hesr3 are essential to generate undifferentiated quiescent satellite cells and to maintain satellite cell numbers
-
Fukada, S., Yamaguchi, M., Kokubo, H., Ogawa, R., Uezumi, A., Yoneda, T., Matev, M.M., Motohashi, N., Ito, T., Zolkiewska, A. et al. (2011) Hesr1 and Hesr3 are essential to generate undifferentiated quiescent satellite cells and to maintain satellite cell numbers. Development, 138, 4609-4619.
-
(2011)
Development
, vol.138
, pp. 4609-4619
-
-
Fukada, S.1
Yamaguchi, M.2
Kokubo, H.3
Ogawa, R.4
Uezumi, A.5
Yoneda, T.6
Matev, M.M.7
Motohashi, N.8
Ito, T.9
Zolkiewska, A.10
-
48
-
-
53049103985
-
Suppression of macrophage functions impairs skeletal muscle regeneration with severe fibrosis
-
Segawa, M., Fukada, S., Yamamoto, Y., Yahagi, H., Kanematsu, M., Sato, M., Ito, T., Uezumi, A., Hayashi, S., Miyagoe-Suzuki, Y. et al. (2008) Suppression of macrophage functions impairs skeletal muscle regeneration with severe fibrosis. Exp. Cell Res., 314, 3232-3244.
-
(2008)
Exp. Cell Res.
, vol.314
, pp. 3232-3244
-
-
Segawa, M.1
Fukada, S.2
Yamamoto, Y.3
Yahagi, H.4
Kanematsu, M.5
Sato, M.6
Ito, T.7
Uezumi, A.8
Hayashi, S.9
Miyagoe-Suzuki, Y.10
-
49
-
-
80052594894
-
Improvement of cardiac fibrosis in dystrophic mice by rAAV9-mediated microdystrophin transduction
-
Shin, J.H., Nitahara-Kasahara, Y., Hayashita-Kinoh, H., Ohshima-Hosoyama, S., Kinoshita, K., Chiyo, T., Okada, H., Okada, T. and Takeda, S. (2011) Improvement of cardiac fibrosis in dystrophic mice by rAAV9-mediated microdystrophin transduction. Gene Ther., 18, 910-919.
-
(2011)
Gene Ther.
, vol.18
, pp. 910-919
-
-
Shin, J.H.1
Nitahara-Kasahara, Y.2
Hayashita-Kinoh, H.3
Ohshima-Hosoyama, S.4
Kinoshita, K.5
Chiyo, T.6
Okada, H.7
Okada, T.8
Takeda, S.9
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