-
1
-
-
33749248495
-
Congenital muscular dystrophies and the extracellular matrix
-
Schessl J, Zou Y, Bönnemann CG. Congenital muscular dystrophies and the extracellular matrix. Semin Pediatr Neurol 2006;13:80-9.
-
(2006)
Semin Pediatr Neurol
, vol.13
, pp. 80-89
-
-
Schessl, J.1
Zou, Y.2
Bönnemann, C.G.3
-
2
-
-
0003074578
-
Fukuyama type congenital progressive muscular dystrophy
-
Fukuyama Y, Osawa M, Saito K, editors, Amsterdam: Elsevier;
-
Osawa M, Sumida S, Suzuki N, et al. Fukuyama type congenital progressive muscular dystrophy. In: Fukuyama Y, Osawa M, Saito K, editors. Congenital Muscular Dystrophies. Amsterdam: Elsevier; 1997. p. 31-68.
-
(1997)
Congenital Muscular Dystrophies
, pp. 31-68
-
-
Osawa, M.1
Sumida, S.2
Suzuki, N.3
-
3
-
-
0032560851
-
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy
-
Kobayashi K, Nakahori Y, Miyake M, et al. An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy. Nature 1998;394:388-92.
-
(1998)
Nature
, vol.394
, pp. 388-392
-
-
Kobayashi, K.1
Nakahori, Y.2
Miyake, M.3
-
4
-
-
0035838362
-
Selective deficiency of α-dystroglycan in Fukuyama-type congenital muscular dystrophy
-
Hayashi YK, Ogawa M, Tagawa K, et al. Selective deficiency of α-dystroglycan in Fukuyama-type congenital muscular dystrophy. Neurology 2001;57:115-21.
-
(2001)
Neurology
, vol.57
, pp. 115-121
-
-
Hayashi, Y.K.1
Ogawa, M.2
Tagawa, K.3
-
5
-
-
33644745063
-
The dystroglycanopathies: The new disorders of O-linked glycosylation
-
Martin PT. The dystroglycanopathies: The new disorders of O-linked glycosylation. Semin Pediatr Neurol 2005;152:152-8.
-
(2005)
Semin Pediatr Neurol
, vol.152
, pp. 152-158
-
-
Martin, P.T.1
-
6
-
-
0038392675
-
Loss-of-function of an N-acetylglucosaminyltransferase, POMGnT1, in muscle-eye-brain disease
-
Manya H. Sakai K, Kobayashi K, et al. Loss-of-function of an N-acetylglucosaminyltransferase, POMGnT1, in muscle-eye-brain disease. Biochem Biophys Res Commun 2003;306:93-7.
-
(2003)
Biochem Biophys Res Commun
, vol.306
, pp. 93-97
-
-
Manya, H.1
Sakai, K.2
Kobayashi, K.3
-
7
-
-
0035095886
-
A new β1,2-N-acetylglucosaminyltransferase that may play a role in the biosynthesis of mammalian O-mannosyl glycans
-
Takahashi S, Sasaki T, Manya H, et al. A new β1,2-N-acetylglucosaminyltransferase that may play a role in the biosynthesis of mammalian O-mannosyl glycans. Glycobiology 2001;11:37-45.
-
(2001)
Glycobiology
, vol.11
, pp. 37-45
-
-
Takahashi, S.1
Sasaki, T.2
Manya, H.3
-
8
-
-
0347635516
-
Demonstration of mammalian protein O-mannosyltransferase activity: Coexpression of POMT1 and POMT2 required for enzymatic activity
-
Manya H, Chiba A, Yoshida A, et al. Demonstration of mammalian protein O-mannosyltransferase activity: coexpression of POMT1 and POMT2 required for enzymatic activity. Proc Acad Natl Sci USA 2004;101:500-5.
-
(2004)
Proc Acad Natl Sci USA
, vol.101
, pp. 500-505
-
-
Manya, H.1
Chiba, A.2
Yoshida, A.3
-
9
-
-
12444307485
-
Expression and localization of fukutin. POMGnT1 and POMT1 in the central nervous system: Consideration for functions of fukutin
-
Yamamoto T, Kato Y, Kawaguchi M, et al. Expression and localization of fukutin. POMGnT1 and POMT1 in the central nervous system: consideration for functions of fukutin. Med Electron Microsc 2004;37:200-7.
-
(2004)
Med Electron Microsc
, vol.37
, pp. 200-207
-
-
Yamamoto, T.1
Kato, Y.2
Kawaguchi, M.3
-
10
-
-
0038327559
-
Aberrant neuronal migration in the brainstem of Fukuyama-type congenital muscular dystrophy
-
Saito Y, Kobayashi M, Itoh M, et al. Aberrant neuronal migration in the brainstem of Fukuyama-type congenital muscular dystrophy. J Neuropathol Exp Neurol 2003;62:497-508.
-
(2003)
J Neuropathol Exp Neurol
, vol.62
, pp. 497-508
-
-
Saito, Y.1
Kobayashi, M.2
Itoh, M.3
-
11
-
-
19344371570
-
Effects of fukutin deficiency in the developing mouse brain
-
Chiyonobu T, Sasaki J, Nagai Y, et al. Effects of fukutin deficiency in the developing mouse brain. Neuromusc Disord 2005;15:416-26.
-
(2005)
Neuromusc Disord
, vol.15
, pp. 416-426
-
-
Chiyonobu, T.1
Sasaki, J.2
Nagai, Y.3
-
12
-
-
0036938777
-
Fukutin expression in glial cells and neurons: Implication in the brain lesions of Fukuyama congenital muscular dystrophy
-
Yamamoto T, Kato Y, Karita M, et al. Fukutin expression in glial cells and neurons: implication in the brain lesions of Fukuyama congenital muscular dystrophy. Acta Neuropathol 2002;104:217-24.
-
(2002)
Acta Neuropathol
, vol.104
, pp. 217-224
-
-
Yamamoto, T.1
Kato, Y.2
Karita, M.3
-
13
-
-
33750986829
-
Intracellular binding of fukutin and α-dystroglycan: Relation glycosylation of α-dystroglycan
-
Yamamoto T, Kawaguchi M, Sakayori N, et al. Intracellular binding of fukutin and α-dystroglycan: relation glycosylation of α-dystroglycan. Neurosci Res 2006;56:391-9.
-
(2006)
Neurosci Res
, vol.56
, pp. 391-399
-
-
Yamamoto, T.1
Kawaguchi, M.2
Sakayori, N.3
-
14
-
-
0036880344
-
Oxidative stress in the brain of Fukuyama type congenital muscular dystrophy: Immunohistochemical study on astrocytes
-
Yamamoto T, Shibata N, Kobayashi M, et al. Oxidative stress in the brain of Fukuyama type congenital muscular dystrophy: immunohistochemical study on astrocytes. J Child Neurol 2002;17:793-9.
-
(2002)
J Child Neurol
, vol.17
, pp. 793-799
-
-
Yamamoto, T.1
Shibata, N.2
Kobayashi, M.3
-
16
-
-
34250018263
-
Dystroglycan regulates structure, proliferation and differentiation of neuroepithelial cells in the developing vertebrate CNS
-
Schröder JE, Tegeler MR, Großhans U, et al. Dystroglycan regulates structure, proliferation and differentiation of neuroepithelial cells in the developing vertebrate CNS. Dev Biol 2007; 307:62-78.
-
(2007)
Dev Biol
, vol.307
, pp. 62-78
-
-
Schröder, J.E.1
Tegeler, M.R.2
Großhans, U.3
-
17
-
-
0037173629
-
Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy
-
Moore SA, Saito F, Chen J, et al. Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy. Nature 2002;418:422-5.
-
(2002)
Nature
, vol.418
, pp. 422-425
-
-
Moore, S.A.1
Saito, F.2
Chen, J.3
-
18
-
-
33644893128
-
Altered glycosylation of α-dystroglycan in neurons of Fukuyama congenital muscular dystrophy brains
-
Saito Y, Yamamoto T, Mizuguchi M, et al. Altered glycosylation of α-dystroglycan in neurons of Fukuyama congenital muscular dystrophy brains. Brain Res 2006;1075:223-8.
-
(2006)
Brain Res
, vol.1075
, pp. 223-228
-
-
Saito, Y.1
Yamamoto, T.2
Mizuguchi, M.3
-
19
-
-
34249786552
-
Defective peripheral nerve myelination and neuromuscular junction formation in fukutin-deficient chimeric mice
-
Saito F, Masaki T, Saito Y, et al. Defective peripheral nerve myelination and neuromuscular junction formation in fukutin-deficient chimeric mice. J Neurochem 2007;101:1712-22.
-
(2007)
J Neurochem
, vol.101
, pp. 1712-1722
-
-
Saito, F.1
Masaki, T.2
Saito, Y.3
-
20
-
-
34249018388
-
Identification of dystroglycan as a second laminin receptor in oligodentrocytes, with a role in myelination
-
Colognato H, Galvin J, Wang Z, et al. Identification of dystroglycan as a second laminin receptor in oligodentrocytes, with a role in myelination. Development 2007;134:1723-36.
-
(2007)
Development
, vol.134
, pp. 1723-1736
-
-
Colognato, H.1
Galvin, J.2
Wang, Z.3
-
21
-
-
34248679918
-
Vascular matrix adhesion and the blood-brain barrier
-
del Zoppo GJ, Milner R, Mabuchi T, et al. Vascular matrix adhesion and the blood-brain barrier. Biochem Soc Transac 2006;34:1261-6.
-
(2006)
Biochem Soc Transac
, vol.34
, pp. 1261-1266
-
-
del Zoppo, G.J.1
Milner, R.2
Mabuchi, T.3
-
22
-
-
2142814283
-
Altered blood-brain barrier development in dystrophic mdx mice
-
Nico B, Nicchia GP, Frigeri A, et al. Altered blood-brain barrier development in dystrophic mdx mice. Neuroscience 2004;125:921-35.
-
(2004)
Neuroscience
, vol.125
, pp. 921-935
-
-
Nico, B.1
Nicchia, G.P.2
Frigeri, A.3
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