-
1
-
-
0025815479
-
Membrane organization of the dystrophin-glycoprotein complex
-
Ervasti, J.M. and Campbell, K.P. (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
-
2
-
-
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
-
3
-
-
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., and Campbell, K.P. (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
Campbell, K.P.11
-
4
-
-
84868028000
-
O-Mannose and O-N-acetyl galactosamine glycosylation of mammalian alpha-dystroglycan is conserved in a region-specific manner
-
Gomez Toledo, A., Raducu, M., Cruces, J., Nilsson, J., Halim, A., Larson, G., Ruetschi, U., and Grahn, A. (2012) O-Mannose and O-N-acetyl galactosamine glycosylation of mammalian alpha-dystroglycan is conserved in a region-specific manner. Glycobiology 22, 1413-1423
-
(2012)
Glycobiology
, vol.22
, pp. 1413-1423
-
-
Gomez Toledo, A.1
Raducu, M.2
Cruces, J.3
Nilsson, J.4
Halim, A.5
Larson, G.6
Ruetschi, U.7
Grahn, A.8
-
5
-
-
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
-
6
-
-
0037173629
-
Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy
-
Moore, S.A., Saito, F., Chen, J., Michele, D.E., Henry, M.D., Messing, A., Cohn, R.D., Ross-Barta, S.E., Westra, S., Williamson, R.A., Hoshi, T., and Campbell, K.P. (2002) Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy. Nature 418, 422-425
-
(2002)
Nature
, vol.418
, pp. 422-425
-
-
Moore, S.A.1
Saito, F.2
Chen, J.3
Michele, D.E.4
Henry, M.D.5
Messing, A.6
Cohn, R.D.7
Ross-Barta, S.E.8
Westra, S.9
Williamson, R.A.10
Hoshi, T.11
Campbell, K.P.12
-
7
-
-
0037709890
-
Unique role of dystroglycan in peripheral nerve myelination, nodal structure, and sodium channel stabilization
-
Saito, F., Moore, S.A., Barresi, R., Henry, M.D., Messing, A., Ross-Barta, S.E., Cohn, R.D., Williamson, R.A., Sluka, K.A., Sherman, D.L., Brophy, P.J., Schmelzer, J.D., Low, P.A., Wrabetz, L., Feltri, M.L., and Campbell, K.P. (2003) Unique role of dystroglycan in peripheral nerve myelination, nodal structure, and sodium channel stabilization. Neuron 38, 747-758
-
(2003)
Neuron
, vol.38
, pp. 747-758
-
-
Saito, F.1
Moore, S.A.2
Barresi, R.3
Henry, M.D.4
Messing, A.5
Ross-Barta, S.E.6
Cohn, R.D.7
Williamson, R.A.8
Sluka, K.A.9
Sherman, D.L.10
Brophy, P.J.11
Schmelzer, J.D.12
Low, P.A.13
Wrabetz, L.14
Feltri, M.L.15
Campbell, K.P.16
-
8
-
-
79952071728
-
Decoding arenavirus pathogenesis: Essential roles for alpha-dystroglycan-virus interactions and the immune response
-
Oldstone, M.B. and Campbell, K.P. (2011) Decoding arenavirus pathogenesis: essential roles for alpha-dystroglycan-virus interactions and the immune response. Virology 411, 170-179
-
(2011)
Virology
, vol.411
, pp. 170-179
-
-
Oldstone, M.B.1
Campbell, K.P.2
-
9
-
-
84880633496
-
Protein O-mannosylation: What we have learned from baker's yeast
-
Loibl, M. and Strahl, S. (2013) Protein O-mannosylation: what we have learned from baker's yeast. Biochim. Biophys. Acta 1833, 2438-2446
-
(2013)
Biochim. Biophys. Acta
, vol.1833
, pp. 2438-2446
-
-
Loibl, M.1
Strahl, S.2
-
10
-
-
0031026624
-
Structures of sialylated o-linked oligosaccharides of bovine peripheral nerve alpha-dystroglycan,the role of a novel o-mannosyl-type oligosaccharide in the binding of alpha-dystroglycan with laminin
-
Chiba, A., Matsumura, K., Yamada, H., Inazu, T., Shimizu, T., Kusunoki, S., Kanazawa, I., Kobata, A., and Endo, T. (1997) Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve alpha-dystroglycan. The role of a novel O-mannosyl-type oligosaccharide in the binding of alpha-dystroglycan with laminin. 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
-
11
-
-
0031790636
-
Detection of O-mannosyl glycans in rabbit skeletal muscle alpha-dystroglycan
-
Sasaki, T., Yamada, H., Matsumura, K., Shimizu, T., Kobata, A., and Endo, T. (1998) Detection of O-mannosyl glycans in rabbit skeletal muscle alpha-dystroglycan. Biochim. Biophys. Acta 1425, 599-606
-
(1998)
Biochim. Biophys. Acta
, vol.1425
, pp. 599-606
-
-
Sasaki, T.1
Yamada, H.2
Matsumura, K.3
Shimizu, T.4
Kobata, A.5
Endo, T.6
-
12
-
-
0031004767
-
Brain contains HNK-1 immunoreactive O-glycans of the sulfoglucuronyl lactosamine series that terminate in 2-linked or 2,6-linked hexose (mannose)
-
Yuen, C.T., Chai, W., Loveless, R.W., Lawson, A.M., Margolis, R.U., and Feizi, T. (1997) Brain contains HNK-1 immunoreactive O-glycans of the sulfoglucuronyl lactosamine series that terminate in 2-linked or 2,6-linked hexose (mannose). J. Biol. Chem. 272, 8924-8931
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 8924-8931
-
-
Yuen, C.T.1
Chai, W.2
Loveless, R.W.3
Lawson, A.M.4
Margolis, R.U.5
Feizi, T.6
-
13
-
-
0032508544
-
Structural analysis of sequences O-linked to mannose reveals a novel Lewis X structure in cranin (dystroglycan) purified from sheep brain
-
Smalheiser, N.R., Haslam, S.M., Sutton-Smith, M., Morris, H.R., and Dell, A. (1998) Structural analysis of sequences O-linked to mannose reveals a novel Lewis X structure in cranin (dystroglycan) purified from sheep brain. J. Biol. Chem. 273, 23698-23703
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 23698-23703
-
-
Smalheiser, N.R.1
Haslam, S.M.2
Sutton-Smith, M.3
Morris, H.R.4
Dell, A.5
-
14
-
-
0033179169
-
High prevalence of 2-mono-and 2,6-di-substituted manol-terminating sequences among O-glycans released from brain glycopeptides by reductive alkaline hydrolysis
-
Chai, W., Yuen, C.T., Kogelberg, H., Carruthers, R.A., Margolis, R.U., Feizi, T., and Lawson, A.M. (1999) High prevalence of 2-mono-and 2,6-di-substituted manol-terminating sequences among O-glycans released from brain glycopeptides by reductive alkaline hydrolysis. Eur. J. Biochem. 263, 879-888
-
(1999)
Eur. J. Biochem.
, vol.263
, pp. 879-888
-
-
Chai, W.1
Yuen, C.T.2
Kogelberg, H.3
Carruthers, R.A.4
Margolis, R.U.5
Feizi, T.6
Lawson, A.M.7
-
15
-
-
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
-
16
-
-
84882923644
-
SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function
-
Yoshida-Moriguchi, T., Willer, T., Anderson, M.E., Venzke, D., Whyte, T., Muntoni, F., Lee, H., Nelson, S.F., Yu, L., and Campbell, K.P. (2013) SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function. Science 341, 896-899
-
(2013)
Science
, vol.341
, pp. 896-899
-
-
Yoshida-Moriguchi, T.1
Willer, T.2
Anderson, M.E.3
Venzke, D.4
Whyte, T.5
Muntoni, F.6
Lee, H.7
Nelson, S.F.8
Yu, L.9
Campbell, K.P.10
-
17
-
-
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. U.S.A. 101, 500-505
-
(2004)
Proc. Natl. Acad. Sci. U.S.A
, 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
-
18
-
-
77249095040
-
Role of N-glycans in maintaining the activity of protein O-mannosyltransferases POMT1 and POMT2
-
Manya, H., Akasaka-Manya, K., Nakajima, A., Kawakita, M., and Endo, T. (2010) Role of N-glycans in maintaining the activity of protein O-mannosyltransferases POMT1 and POMT2. J. Biochem. 147, 337-344
-
(2010)
J. Biochem.
, vol.147
, pp. 337-344
-
-
Manya, H.1
Akasaka-Manya, K.2
Nakajima, A.3
Kawakita, M.4
Endo, T.5
-
19
-
-
0033152809
-
Identification of a human homolog of the Drosophila rotated abdomen gene (POMT1) encoding a putative protein O-mannosyl-transferase, and assignment to human chromosome 9q34.1
-
Jurado, L.A., Coloma, A., and Cruces, J. (1999) Identification of a human homolog of the Drosophila rotated abdomen gene (POMT1) encoding a putative protein O-mannosyl-transferase, and assignment to human chromosome 9q34.1. Genomics 58, 171-180
-
(1999)
Genomics
, vol.58
, pp. 171-180
-
-
Jurado, L.A.1
Coloma, A.2
Cruces, J.3
-
20
-
-
0036869334
-
Characterization of POMT2, a novel member of the PMT protein O-mannosyltransferase family specifically localized to the acrosome of mammalian spermatids
-
Willer, T., Amselgruber, W., Deutzmann, R., and Strahl, S. (2002) Characterization of POMT2, a novel member of the PMT protein O-mannosyltransferase family specifically localized to the acrosome of mammalian spermatids. Glycobiology 12, 771-783
-
(2002)
Glycobiology
, vol.12
, pp. 771-783
-
-
Willer, T.1
Amselgruber, W.2
Deutzmann, R.3
Strahl, S.4
-
21
-
-
84877975094
-
Futile protein folding cycles in the ER are terminated by the unfolded protein O-mannosylation pathway
-
Xu, C., Wang, S., Thibault, G., and Ng, D.T. (2013) Futile protein folding cycles in the ER are terminated by the unfolded protein O-mannosylation pathway. Science 340, 978-981
-
(2013)
Science
, vol.340
, pp. 978-981
-
-
Xu, C.1
Wang, S.2
Thibault, G.3
Ng, D.T.4
-
22
-
-
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., Herrmann, R., Straub, V., Talim, B., Voit, T., Topaloglu, H., Toda, T., and Endo, T. (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
Herrmann, R.11
Straub, V.12
Talim, B.13
Voit, T.14
Topaloglu, H.15
Toda, T.16
Endo, T.17
-
23
-
-
2942672066
-
Structure-function analysis of human protein O-linked mannose b1,2-N-acetylglucosaminyltransferase 1, POMGnT1
-
Akasaka-Manya, K., Manya, H., Kobayashi, K., Toda, T., and Endo, T. (2004) Structure-function analysis of human protein O-linked mannose b1,2-N-acetylglucosaminyltransferase 1, POMGnT1. Biochem. Biophys. Res. Commun. 320, 39-44
-
(2004)
Biochem. Biophys. Res. Commun.
, vol.320
, pp. 39-44
-
-
Akasaka-Manya, K.1
Manya, H.2
Kobayashi, K.3
Toda, T.4
Endo, T.5
-
24
-
-
0035095886
-
A new beta-1,2-N-acetylglucosaminyltransferase that may play a role in the biosynthesis of mammalian O-mannosyl glycans
-
Takahashi, S., Sasaki, T., Manya, H., Chiba, Y., Yoshida, A., Mizuno, M., Ishida, H., Ito, F., Inazu, T., Kotani, N., Takasaki, S., Takeuchi, M., and Endo, T. (2001) A new beta-1,2-N-acetylglucosaminyltransferase that may play a role in the biosynthesis of mammalian O-mannosyl glycans. Glycobiology 11, 37-45
-
(2001)
Glycobiology
, vol.11
, pp. 37-45
-
-
Takahashi, S.1
Sasaki, T.2
Manya, H.3
Chiba, Y.4
Yoshida, A.5
Mizuno, M.6
Ishida, H.7
Ito, F.8
Inazu, T.9
Kotani, N.10
Takasaki, S.11
Takeuchi, M.12
Endo, T.13
-
25
-
-
79960045861
-
Effects of length and amino acid sequence of O-mannosyl peptides on substrate specificity of protein O-linked mannose beta1,2-N-acetylglucosaminyltransferase 1 (POMGnT1)
-
Akasaka-Manya, K., Manya, H., Mizuno, M., Inazu, T., and Endo, T. (2011) Effects of length and amino acid sequence of O-mannosyl peptides on substrate specificity of protein O-linked mannose beta1,2-N-acetylglucosaminyltransferase 1 (POMGnT1). Biochem. Biophys. Res. Commun. 410, 632-636
-
(2011)
Biochem. Biophys. Res. Commun.
, vol.410
, pp. 632-636
-
-
Akasaka-Manya, K.1
Manya, H.2
Mizuno, M.3
Inazu, T.4
Endo, T.5
-
26
-
-
84887401948
-
O-glycosylation of the non-canonical T-cadherin from rabbit skeletal muscle by single mannose residues
-
Winterhalter, P.R., Lommel, M., Ruppert, T., and Strahl, S. (2013) O-glycosylation of the non-canonical T-cadherin from rabbit skeletal muscle by single mannose residues. FEBS Lett. 587, 3715-3721
-
(2013)
FEBS Lett.
, vol.587
, pp. 3715-3721
-
-
Winterhalter, P.R.1
Lommel, M.2
Ruppert, T.3
Strahl, S.4
-
27
-
-
0242541626
-
A novel beta(1,6)-N-acetylglucosaminyltransferase v (GnT-VB)(1)
-
Kaneko, M., Alvarez-Manilla, G., Kamar, M., Lee, I., Lee, J.K., Troupe, K., Zhang, W., Osawa, M., and Pierce, M. (2003) A novel beta(1,6)-N-acetylglucosaminyltransferase V (GnT-VB)(1). FEBS Lett. 554, 515-519
-
(2003)
FEBS Lett.
, vol.554
, pp. 515-519
-
-
Kaneko, M.1
Alvarez-Manilla, G.2
Kamar, M.3
Lee, I.4
Lee, J.K.5
Troupe, K.6
Zhang, W.7
Osawa, M.8
Pierce, M.9
-
28
-
-
0242322005
-
Molecular cloning and characterization of human GnT-IX, a novel beta1,6-Nacetylglucosaminyltransferase that is specifically expressed in the brain
-
Inamori, K., Endo, T., Ide, Y., Fujii, S., Gu, J., Honke, K., and Taniguchi, N. (2003) Molecular cloning and characterization of human GnT-IX, a novel beta1,6-Nacetylglucosaminyltransferase that is specifically expressed in the brain. J. Biol. Chem. 278, 43102-43109
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 43102-43109
-
-
Inamori, K.1
Endo, T.2
Ide, Y.3
Fujii, S.4
Gu, J.5
Honke, K.6
Taniguchi, N.7
-
29
-
-
9144252532
-
N-Acetylglucosaminyltransferase IX acts on the GlcNAc beta 1,2-Man alpha 1-Ser/Thr moiety, forming a 2,6-branched structure in brain Omannosyl glycan
-
Inamori, K., Endo, T., Gu, J., Matsuo, I., Ito, Y., Fujii, S., Iwasaki, H., Narimatsu, H., Miyoshi, E., Honke, K., and Taniguchi, N. (2004) N-Acetylglucosaminyltransferase IX acts on the GlcNAc beta 1,2-Man alpha 1-Ser/Thr moiety, forming a 2,6-branched structure in brain Omannosyl glycan. J. Biol. Chem. 279, 2337-2340
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 2337-2340
-
-
Inamori, K.1
Endo, T.2
Gu, J.3
Matsuo, I.4
Ito, Y.5
Fujii, S.6
Iwasaki, H.7
Narimatsu, H.8
Miyoshi, E.9
Honke, K.10
Taniguchi, N.11
-
30
-
-
84878844269
-
Loss of branched O-mannosyl glycans in astrocytes accelerates remyelination
-
Kanekiyo, K., Inamori, K., Kitazume, S., Sato, K., Maeda, J., Higuchi, M., Kizuka, Y., Korekane, H., Matsuo, I., Honke, K., and Taniguchi, N. (2013) Loss of branched O-mannosyl glycans in astrocytes accelerates remyelination. J. Neurosci. 33, 10037-10047
-
(2013)
J. Neurosci.
, vol.33
, pp. 10037-10047
-
-
Kanekiyo, K.1
Inamori, K.2
Kitazume, S.3
Sato, K.4
Maeda, J.5
Higuchi, M.6
Kizuka, Y.7
Korekane, H.8
Matsuo, I.9
Honke, K.10
Taniguchi, N.11
-
31
-
-
57749114758
-
Receptor tyrosine phosphatase beta (RPTPbeta) activity and signaling are attenuated by glycosylation and subsequent cell surface galectin-1 binding
-
Abbott, K.L., Matthews, R.T., and Pierce, M. (2008) Receptor tyrosine phosphatase beta (RPTPbeta) activity and signaling are attenuated by glycosylation and subsequent cell surface galectin-1 binding. J. Biol. Chem. 283, 33026-33035
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 33026-33035
-
-
Abbott, K.L.1
Matthews, R.T.2
Pierce, M.3
-
32
-
-
84894270094
-
Structural and biochemical characterization of O-mannose-linked human natural killer-1 glycan expressed on phosphacan in developing mouse brains
-
Morise, J., Kizuka, Y., Yabuno, K., Tonoyama, Y., Hashii, N., Kawasaki, N., Manya, H., Miyagoe-Suzuki, Y., Takeda, S., Endo, T., Maeda, N., Takematsu, H., and Oka, S. (2014) Structural and biochemical characterization of O-mannose-linked human natural killer-1 glycan expressed on phosphacan in developing mouse brains. Glycobiology 24, 314-324
-
(2014)
Glycobiology
, vol.24
, pp. 314-324
-
-
Morise, J.1
Kizuka, Y.2
Yabuno, K.3
Tonoyama, Y.4
Hashii, N.5
Kawasaki, N.6
Manya, H.7
Miyagoe-Suzuki, Y.8
Takeda, S.9
Endo, T.10
Maeda, N.11
Takematsu, H.12
Oka, S.13
-
33
-
-
20444496822
-
Beta4GalT-II is a key regulator of glycosylation of the proteins involved in neuronal development
-
Sasaki, N., Manya, H., Okubo, R., Kobayashi, K., Ishida, H., Toda, T., Endo, T., and Nishihara, S. (2005) beta4GalT-II is a key regulator of glycosylation of the proteins involved in neuronal development. Biochem. Biophys. Res. Commun. 333, 131-137
-
(2005)
Biochem. Biophys. Res. Commun.
, vol.333
, pp. 131-137
-
-
Sasaki, N.1
Manya, H.2
Okubo, R.3
Kobayashi, K.4
Ishida, H.5
Toda, T.6
Endo, T.7
Nishihara, S.8
-
34
-
-
84874834197
-
Xylosyl-and glucuronyltransferase functions of LARGE in alpha-dystroglycan modification are conserved in LARGE2
-
Inamori, K., Hara, Y., Willer, T., Anderson, M.E., Zhu, Z., Yoshida-Moriguchi, T., and Campbell, K.P. (2013) Xylosyl-and glucuronyltransferase functions of LARGE in alpha-dystroglycan modification are conserved in LARGE2. Glycobiology 23, 295-302
-
(2013)
Glycobiology
, vol.23
, pp. 295-302
-
-
Inamori, K.1
Hara, Y.2
Willer, T.3
Anderson, M.E.4
Zhu, Z.5
Yoshida-Moriguchi, T.6
Campbell, K.P.7
-
35
-
-
84865744996
-
Human natural killer-1 sulfotransferase (HNK-1ST)-induced sulfate transfer regulates laminin-binding glycans on alpha-dystroglycan
-
Nakagawa, N., Manya, H., Toda, T., Endo, T., and Oka, S. (2012) Human natural killer-1 sulfotransferase (HNK-1ST)-induced sulfate transfer regulates laminin-binding glycans on alpha-dystroglycan. J. Biol. Chem. 287, 30823-30832
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 30823-30832
-
-
Nakagawa, N.1
Manya, H.2
Toda, T.3
Endo, T.4
Oka, S.5
-
36
-
-
84875730533
-
LARGE2 generates the same xylose-and glucuronic acid-containing glycan structures as LARGE
-
Ashikov, A., Buettner, F.F., Tiemann, B., Gerardy-Schahn, R., and Bakker, H. (2013) LARGE2 generates the same xylose-and glucuronic acid-containing glycan structures as LARGE. Glycobiology 23, 303-309
-
(2013)
Glycobiology
, vol.23
, pp. 303-309
-
-
Ashikov, A.1
Buettner, F.F.2
Tiemann, B.3
Gerardy-Schahn, R.4
Bakker, H.5
-
37
-
-
59849123266
-
Reduced proliferative activity of primary POMGnT1-null myoblasts in vitro
-
Miyagoe-Suzuki, Y., Masubuchi, N., Miyamoto, K., Wada, M.R., Yuasa, S., Saito, F., Matsumura, K., Kanesaki, H., Kudo, A., Manya, H., Endo, T., and Takeda, S. (2009) Reduced proliferative activity of primary POMGnT1-null myoblasts in vitro. Mech. Dev. 126, 107-116
-
(2009)
Mech. Dev.
, vol.126
, pp. 107-116
-
-
Miyagoe-Suzuki, Y.1
Masubuchi, N.2
Miyamoto, K.3
Wada, M.R.4
Yuasa, S.5
Saito, F.6
Matsumura, K.7
Kanesaki, H.8
Kudo, A.9
Manya, H.10
Endo, T.11
Takeda, S.12
-
38
-
-
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., Nagai, Y., Tashiro, F., Miyazaki, J., Tajima, Y., Endo, T., Kobayashi, K., Campbell, K.P., and Toda, T. (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
Nagai, Y.11
Tashiro, F.12
Miyazaki, J.13
Tajima, Y.14
Endo, T.15
Kobayashi, K.16
Campbell, K.P.17
Toda, T.18
-
39
-
-
84887405820
-
LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy
-
Goddeeris, M.M., Wu, B., Venzke, D., Yoshida-Moriguchi, T., Saito, F., Matsumura, K., Moore, S.A., and Campbell, K.P. (2013) LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy. Nature 503, 136-140
-
(2013)
Nature
, vol.503
, pp. 136-140
-
-
Goddeeris, M.M.1
Wu, B.2
Venzke, D.3
Yoshida-Moriguchi, T.4
Saito, F.5
Matsumura, K.6
Moore, S.A.7
Campbell, K.P.8
-
40
-
-
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
-
41
-
-
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
-
42
-
-
0031770342
-
The relationship between perlecan and dystroglycan and its implication in the formation of the neuromuscular junction
-
Peng, H.B., Ali, A.A., Daggett, D.F., Rauvala, H., Hassell, J.R., and Smalheiser, N.R. (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
-
43
-
-
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
-
44
-
-
48149109425
-
Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation
-
Sato, S., Omori, Y., Katoh, K., Kondo, M., Kanagawa, M., Miyata, K., Funabiki, K., Koyasu, T., Kajimura, N., Miyoshi, T., Sawai, H., Kobayashi, K., Tani, A., Toda, T., Usukura, J., Tano, Y., Fujikado, T., and Furukawa, T. (2008) Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation. Nat. Neurosci. 11, 923-931
-
(2008)
Nat. Neurosci.
, vol.11
, pp. 923-931
-
-
Sato, S.1
Omori, Y.2
Katoh, K.3
Kondo, M.4
Kanagawa, M.5
Miyata, K.6
Funabiki, K.7
Koyasu, T.8
Kajimura, N.9
Miyoshi, T.10
Sawai, H.11
Kobayashi, K.12
Tani, A.13
Toda, T.14
Usukura, J.15
Tano, Y.16
Fujikado, T.17
Furukawa, T.18
-
45
-
-
84872696903
-
Dystroglycan organizes axon guidance cue localization and axonal pathfinding
-
Wright, K.M., Lyon, K.A., Leung, H., Leahy, D.J., Ma, L., and Ginty, D.D. (2012) Dystroglycan organizes axon guidance cue localization and axonal pathfinding. Neuron 76, 931-944
-
(2012)
Neuron
, vol.76
, pp. 931-944
-
-
Wright, K.M.1
Lyon, K.A.2
Leung, H.3
Leahy, D.J.4
Ma, L.5
Ginty, D.D.6
-
46
-
-
84858598482
-
Absence of post-phosphoryl modification in dystroglycanopathy mouse models and wild-type tissues expressing non-laminin binding form of alpha-dystroglycan
-
Kuga, A., Kanagawa, M., Sudo, A., Chan, Y.M., Tajiri, M., Manya, H., Kikkawa, Y., Nomizu, M., Kobayashi, K., Endo, T., Lu, Q.L., Wada, Y., and Toda, T. (2012) Absence of post-phosphoryl modification in dystroglycanopathy mouse models and wild-type tissues expressing non-laminin binding form of alpha-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
Lu, Q.L.11
Wada, Y.12
Toda, T.13
-
47
-
-
0030826509
-
Tissue-specific heterogeneity in alpha-dystroglycan sialoglycosylation,skeletal muscle alpha-dystroglycan is a latent receptor for vicia villosa agglutinin b4 masked by sialic acid modification
-
Ervasti, J.M., Burwell, A.L., and Geissler, A.L. (1997) Tissue-specific heterogeneity in alpha-dystroglycan sialoglycosylation. Skeletal muscle alpha-dystroglycan is a latent receptor for Vicia villosa agglutinin b4 masked by sialic acid modification. J. Biol. Chem. 272, 22315-22321
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 22315-22321
-
-
Ervasti, J.M.1
Burwell, A.L.2
Geissler, A.L.3
-
48
-
-
34250639054
-
Characterization of a novel modification on IgG2 light chain,Evidence for the presence of Olinked mannosylation
-
Martinez, T., Pace, D., Brady, L., Gerhart, M., and Balland, A. (2007) Characterization of a novel modification on IgG2 light chain. Evidence for the presence of Olinked mannosylation. J. Chromatogr. A 1156, 183-187
-
(2007)
J. Chromatogr. A
, vol.1156
, pp. 183-187
-
-
Martinez, T.1
Pace, D.2
Brady, L.3
Gerhart, M.4
Balland, A.5
-
49
-
-
68149158726
-
O-glycosylation pattern of CD24 from mouse brain
-
Bleckmann, C., Geyer, H., Lieberoth, A., Splittstoesser, F., Liu, Y., Feizi, T., Schachner, M., Kleene, R., Reinhold, V., and Geyer, R. (2009) O-glycosylation pattern of CD24 from mouse brain. Biol. Chem. 390, 627-645
-
(2009)
Biol. Chem.
, vol.390
, pp. 627-645
-
-
Bleckmann, C.1
Geyer, H.2
Lieberoth, A.3
Splittstoesser, F.4
Liu, Y.5
Feizi, T.6
Schachner, M.7
Kleene, R.8
Reinhold, V.9
Geyer, R.10
-
50
-
-
84864578742
-
Neurofascin 186 is O-mannosylated within and outside of the mucin domain
-
Pacharra, S., Hanisch, F.G., and Breloy, I. (2012) Neurofascin 186 is O-mannosylated within and outside of the mucin domain. J. Proteome Res. 11, 3955-3964
-
(2012)
J. Proteome Res.
, vol.11
, pp. 3955-3964
-
-
Pacharra, S.1
Hanisch, F.G.2
Breloy, I.3
-
51
-
-
84875912842
-
The lecticans of mammalian brain perineural net are O-mannosylated
-
Pacharra, S., Hanisch, F.G., Muhlenhoff, M., Faissner, A., Rauch, U., and Breloy, I. (2013) The lecticans of mammalian brain perineural net are O-mannosylated. J. Proteome Res. 12, 1764-1771
-
(2013)
J. Proteome Res.
, vol.12
, pp. 1764-1771
-
-
Pacharra, S.1
Hanisch, F.G.2
Muhlenhoff, M.3
Faissner, A.4
Rauch, U.5
Breloy, I.6
-
52
-
-
84891368942
-
Mining the O-mannose glycoproteome reveals cadherins as major O-mannosylated glycoproteins
-
Vester-Christensen, M.B., Halim, A., Joshi, H.J., Steentoft, C., Bennett, E.P., Levery, S.B., Vakhrushev, S.Y., and Clausen, H. (2013) Mining the O-mannose glycoproteome reveals cadherins as major O-mannosylated glycoproteins. Proc. Natl. Acad. Sci. U.S.A. 110, 21018-21023
-
(2013)
Proc. Natl. Acad. Sci. U.S.A
, vol.110
, pp. 21018-21023
-
-
Vester-Christensen, M.B.1
Halim, A.2
Joshi, H.J.3
Steentoft, C.4
Bennett, E.P.5
Levery, S.B.6
Vakhrushev, S.Y.7
Clausen, H.8
-
53
-
-
84891363796
-
Protein O-mannosylation is crucial for E-cadherin-mediated cell adhesion
-
Lommel, M., Winterhalter, P.R., Willer, T., Dahlhoff, M., Schneider, M.R., Bartels, M.F., Renner-Muller, I., Ruppert, T., Wolf, E., and Strahl, S. (2013) Protein O-mannosylation is crucial for E-cadherin-mediated cell adhesion. Proc. Natl. Acad. Sci. U.S.A. 110, 21024-21029
-
(2013)
Proc. Natl. Acad. Sci. U.S.A
, vol.110
, pp. 21024-21029
-
-
Lommel, M.1
Winterhalter, P.R.2
Willer, T.3
Dahlhoff, M.4
Schneider, M.R.5
Bartels, M.F.6
Renner-Muller, I.7
Ruppert, T.8
Wolf, E.9
Strahl, S.10
-
54
-
-
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., Jimenez-Mallebrera, C., Mercuri, E., Manzur, A.Y., Kinali, M., Torelli, S., Brown, S.C., Sewry, C.A., Bushby, K., Topaloglu, H., North, K., Abbs, S., and Muntoni, F. (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
Jimenez-Mallebrera, C.11
Mercuri, E.12
Manzur, A.Y.13
Kinali, M.14
Torelli, S.15
Brown, S.C.16
Sewry, C.A.17
Bushby, K.18
Topaloglu, H.19
North, K.20
Abbs, S.21
Muntoni, F.22
more..
-
55
-
-
0038185363
-
Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome
-
Beltran-Valero De Bernabe, D., Currier, S., Steinbrecher, A., Celli, J., Van Beusekom, E., Van Der Zwaag, B., Kayserili, H., Merlini, L., Chitayat, D., Dobyns, W.B., Cormand, B., Lehesjoki, A.E., Cruces, J., Voit, T., Walsh, C.A., Van Bokhoven, H., and Brunner, H.G. (2002) Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome. Am. J. Hum. Genet. 71, 1033-1043
-
(2002)
Am. J. Hum. Genet
, vol.71
, pp. 1033-1043
-
-
Beltran-Valero De Bernabe, D.1
Currier, S.2
Steinbrecher, A.3
Celli, J.4
Van Beusekom, E.5
Van Der Zwaag, B.6
Kayserili, H.7
Merlini, L.8
Chitayat, D.9
Dobyns, W.B.10
Cormand, B.11
Lehesjoki, A.E.12
Cruces, J.13
Voit, T.14
Walsh, C.A.15
Van Bokhoven, H.16
Brunner, H.G.17
-
56
-
-
26944438148
-
POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome
-
van Reeuwijk, J., Janssen, M., van den Elzen, C., Beltran-Valero de Bernabe, D., Sabatelli, P., Merlini, L., Boon, M., Scheffer, H., Brockington, M., Muntoni, F., Huynen, M.A., Verrips, A., Walsh, C.A., Barth, P.G., Brunner, H.G., and van Bokhoven, H. (2005) POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome. J. Med. Genet. 42, 907-912
-
(2005)
J. Med. Genet
, vol.42
, pp. 907-912
-
-
Van Reeuwijk, J.1
Janssen, M.2
Van Den Elzen, C.3
Beltran-Valero De Bernabe, D.4
Sabatelli, P.5
Merlini, L.6
Boon, M.7
Scheffer, H.8
Brockington, M.9
Muntoni, F.10
Huynen, M.A.11
Verrips, A.12
Walsh, C.A.13
Barth, P.G.14
Brunner, H.G.15
Van Bokhoven, H.16
-
57
-
-
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., Hamano, K., Sakakihara, Y., Nonaka, I., Nakagome, Y., Kanazawa, I., Nakamura, Y., Tokunaga, K., and Toda, T. (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
Hamano, K.11
Sakakihara, Y.12
Nonaka, I.13
Nakagome, Y.14
Kanazawa, I.15
Nakamura, Y.16
Tokunaga, K.17
Toda, T.18
-
58
-
-
0035212037
-
Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency 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., Voit, T., Sewry, C.A., Guicheney, P., and Muntoni, F. (2001) Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency 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
Voit, T.11
Sewry, C.A.12
Guicheney, P.13
Muntoni, F.14
-
59
-
-
18244375299
-
Mutations in the fukutinrelated 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., Fallet, S., Romero, N., Fardeau, M., Straub, V., Storey, G., Pollitt, C., Richard, I., Sewry, C.A., Bushby, K., Voit, T., Blake, D.J., and Muntoni, F. (2001) Mutations in the fukutinrelated 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
Fallet, S.11
Romero, N.12
Fardeau, M.13
Straub, V.14
Storey, G.15
Pollitt, C.16
Richard, I.17
Sewry, C.A.18
Bushby, K.19
Voit, T.20
Blake, D.J.21
Muntoni, F.22
more..
-
60
-
-
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., Sewry, C.A., Brown, S.C., and Muntoni, F. (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
Sewry, C.A.11
Brown, S.C.12
Muntoni, F.13
-
61
-
-
84866063186
-
Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome
-
Manzini, M.C., Tambunan, D.E., Hill, R.S., Yu, T.W., Maynard, T.M., Heinzen, E.L., Shianna, K.V., Stevens, C.R., Partlow, J.N., Barry, B.J., Rodriguez, J., Gupta, V.A., Al-Qudah, A.K., Eyaid, W.M., Friedman, J.M., Salih, M.A., Clark, R., Moroni, I., Mora, M., Beggs, A.H., Gabriel, S.B., and Walsh, C.A. (2012) Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome. Am. J. Hum. Genet. 91, 541-547
-
(2012)
Am. J. Hum. Genet
, vol.91
, pp. 541-547
-
-
Manzini, M.C.1
Tambunan, D.E.2
Hill, R.S.3
Yu, T.W.4
Maynard, T.M.5
Heinzen, E.L.6
Shianna, K.V.7
Stevens, C.R.8
Partlow, J.N.9
Barry, B.J.10
Rodriguez, J.11
Gupta, V.A.12
Al-Qudah, A.K.13
Eyaid, W.M.14
Friedman, J.M.15
Salih, M.A.16
Clark, R.17
Moroni, I.18
Mora, M.19
Beggs, A.H.20
Gabriel, S.B.21
Walsh, C.A.22
more..
-
62
-
-
84876414078
-
Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of alpha-dystroglycan
-
Stevens, E., Carss, K.J., Cirak, S., Foley, A.R., Torelli, S., Willer, T., Tambunan, D.E., Yau, S., Brodd, L., Sewry, C.A., Feng, L., Haliloglu, G., Orhan, D., Dobyns, W.B., Enns, G.M., Manning, M., Krause, A., Salih, M.A., Walsh, C.A., Hurles, M., Campbell, K.P., Manzini, M.C., Stemple, D., Lin, Y.Y., and Muntoni, F. (2013) Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of alpha-dystroglycan. Am. J. Hum. Genet. 92, 354-365
-
(2013)
Am. J. Hum. Genet
, vol.92
, pp. 354-365
-
-
Stevens, E.1
Carss, K.J.2
Cirak, S.3
Foley, A.R.4
Torelli, S.5
Willer, T.6
Tambunan, D.E.7
Yau, S.8
Brodd, L.9
Sewry, C.A.10
Feng, L.11
Haliloglu, G.12
Orhan, D.13
Dobyns, W.B.14
Enns, G.M.15
Manning, M.16
Krause, A.17
Salih, M.A.18
Walsh, C.A.19
Hurles, M.20
Campbell, K.P.21
Manzini, M.C.22
Stemple, D.23
Lin, Y.Y.24
Muntoni, F.25
more..
-
63
-
-
1842639492
-
A novel human beta1,3-N-acetylgalactosaminyltransferase that synthesizes a unique carbohydrate structure, GalNAcbeta1-3GlcNAc
-
Hiruma, T., Togayachi, A., Okamura, K., Sato, T., Kikuchi, N., Kwon, Y.D., Nakamura, A., Fujimura, K., Gotoh, M., Tachibana, K., Ishizuka, Y., Noce, T., Nakanishi, H., and Narimatsu, H. (2004) A novel human beta1,3-N-acetylgalactosaminyltransferase that synthesizes a unique carbohydrate structure, GalNAcbeta1-3GlcNAc. J. Biol. Chem. 279, 14087-14095
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 14087-14095
-
-
Hiruma, T.1
Togayachi, A.2
Okamura, K.3
Sato, T.4
Kikuchi, N.5
Kwon, Y.D.6
Nakamura, A.7
Fujimura, K.8
Gotoh, M.9
Tachibana, K.10
Ishizuka, Y.11
Noce, T.12
Nakanishi, H.13
Narimatsu, H.14
-
64
-
-
84875953109
-
Missense mutations in beta-1,3-N-acetylglucosaminyltransferase 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., Babul-Hirji, R., Halliday, W., Wright, G.J., Stemple, D.L., Lin, Y.Y., Lefeber, D.J., and van Bokhoven, H. (2013) Missense mutations in beta-1,3-N-acetylglucosaminyltransferase 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
Babul-Hirji, R.11
Halliday, W.12
Wright, G.J.13
Stemple, D.L.14
Lin, Y.Y.15
Lefeber, D.J.16
Van Bokhoven, H.17
-
65
-
-
0031445110
-
Expression cloning of cDNA encoding a human beta-1,3-N-acetylglucosaminyltransferase that is essential for poly-N-acetyllactosamine synthesis
-
Sasaki, K., Kurata-Miura, K., Ujita, M., Angata, K., Nakagawa, S., Sekine, S., Nishi, T., and Fukuda, M. (1997) Expression cloning of cDNA encoding a human beta-1,3-N-acetylglucosaminyltransferase that is essential for poly-N-acetyllactosamine synthesis. Proc. Natl. Acad. Sci. U.S.A. 94, 14294-14299
-
(1997)
Proc. Natl. Acad. Sci. U.S.A
, vol.94
, pp. 14294-14299
-
-
Sasaki, K.1
Kurata-Miura, K.2
Ujita, M.3
Angata, K.4
Nakagawa, S.5
Sekine, S.6
Nishi, T.7
Fukuda, M.8
-
66
-
-
84876664165
-
Deciphering the glycosylome of dystroglycanopathies using haploid screens for lassa virus entry
-
Jae, L.T., Raaben, M., Riemersma, M., van Beusekom, E., Blomen, V.A., Velds, A., Kerkhoven, R.M., Carette, J.E., Topaloglu, H., Meinecke, P., Wessels, M.W., Lefeber, D.J., Whelan, S.P., van Bokhoven, H., and Brummelkamp, T.R. (2013) Deciphering the glycosylome of dystroglycanopathies using haploid screens for lassa virus entry. Science 340, 479-483
-
(2013)
Science
, vol.340
, pp. 479-483
-
-
Jae, L.T.1
Raaben, M.2
Riemersma, M.3
Van Beusekom, E.4
Blomen, V.A.5
Velds, A.6
Kerkhoven, R.M.7
Carette, J.E.8
Topaloglu, H.9
Meinecke, P.10
Wessels, M.W.11
Lefeber, D.J.12
Whelan, S.P.13
Van Bokhoven, H.14
Brummelkamp, T.R.15
-
67
-
-
84870935092
-
Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephaly
-
Vuillaumier-Barrot, S., Bouchet-Seraphin, C., Chelbi, M., Devisme, L., Quentin, S., Gazal, S., Laquerriere, A., Fallet-Bianco, C., Loget, P., Odent, S., Carles, D., Bazin, A., Aziza, J., Clemenson, A., Guimiot, F., Bonniere, M., Monnot, S., Bole-Feysot, C., Bernard, J.P., Loeuillet, L., Gonzales, M., Socha, K., Grandchamp, B., Attie-Bitach, T., Encha-Razavi, F., and Seta, N. (2012) Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephaly. Am. J. Hum. Genet. 91, 1135-1143
-
(2012)
Am. J. Hum. Genet
, vol.91
, pp. 1135-1143
-
-
Vuillaumier-Barrot, S.1
Bouchet-Seraphin, C.2
Chelbi, M.3
Devisme, L.4
Quentin, S.5
Gazal, S.6
Laquerriere, A.7
Fallet-Bianco, C.8
Loget, P.9
Odent, S.10
Carles, D.11
Bazin, A.12
Aziza, J.13
Clemenson, A.14
Guimiot, F.15
Bonniere, M.16
Monnot, S.17
Bole-Feysot, C.18
Bernard, J.P.19
Loeuillet, L.20
Gonzales, M.21
Socha, K.22
Grandchamp, B.23
Attie-Bitach, T.24
Encha-Razavi, F.25
Seta, N.26
more..
-
68
-
-
84880285119
-
Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of alpha-dystroglycan
-
Carss, K.J., Stevens, E., Foley, A.R., Cirak, S., Riemersma, M., Torelli, S., Hoischen, A., Willer, T., van Scherpenzeel, M., Moore, S.A., Messina, S., Bertini, E., Bonnemann, C.G., Abdenur, J.E., Grosmann, C.M., Kesari, A., Punetha, J., Quinlivan, R., Waddell, L.B., Young, H.K., Wraige, E., Yau, S., Brodd, L., Feng, L., Sewry, C., MacArthur, D.G., North, K.N., Hoffman, E., Stemple, D.L., Hurles, M.E., van Bokhoven, H., Campbell, K.P., Lefeber, D.J., Lin, Y.Y., and Muntoni, F. (2013) Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of alpha-dystroglycan. Am. J. Hum. Genet. 93, 29-41
-
(2013)
Am. J. Hum. Genet
, vol.93
, pp. 29-41
-
-
Carss, K.J.1
Stevens, E.2
Foley, A.R.3
Cirak, S.4
Riemersma, M.5
Torelli, S.6
Hoischen, A.7
Willer, T.8
Van Scherpenzeel, M.9
Moore, S.A.10
Messina, S.11
Bertini, E.12
Bonnemann, C.G.13
Abdenur, J.E.14
Grosmann, C.M.15
Kesari, A.16
Punetha, J.17
Quinlivan, R.18
Waddell, L.B.19
Young, H.K.20
Wraige, E.21
Yau, S.22
Brodd, L.23
Feng, L.24
Sewry, C.25
MacArthur, D.G.26
North, K.N.27
Hoffman, E.28
Stemple, D.L.29
Hurles, M.E.30
Van Bokhoven, H.31
Campbell, K.P.32
Lefeber, D.J.33
Lin, Y.Y.34
Muntoni, F.35
more..
-
69
-
-
0033695039
-
Cloning, expression and characterization of the pig liver GDP-mannose pyrophosphorylase,Evidence that GDP-mannose and GDP-Glc pyrophosphorylases are different proteins
-
Ning, B. and Elbein, A.D. (2000) Cloning, expression and characterization of the pig liver GDP-mannose pyrophosphorylase. Evidence that GDP-mannose and GDP-Glc pyrophosphorylases are different proteins. Eur. J. Biochem. 267, 6866-6874
-
(2000)
Eur. J. Biochem.
, vol.267
, pp. 6866-6874
-
-
Ning, B.1
Elbein, A.D.2
-
70
-
-
84885421942
-
Congenital disorder of glycosylation due to DPM1 mutations presenting with dystroglycanopathy-type congenital muscular dystrophy
-
Yang, A.C., Ng, B.G., Moore, S.A., Rush, J., Waechter, C.J., Raymond, K.M., Willer, T., Campbell, K.P., Freeze, H.H., and Mehta, L. (2013) Congenital disorder of glycosylation due to DPM1 mutations presenting with dystroglycanopathy-type congenital muscular dystrophy. Mol. Genet. Metab. 110, 345-351
-
(2013)
Mol. Genet. Metab
, vol.110
, pp. 345-351
-
-
Yang, A.C.1
Ng, B.G.2
Moore, S.A.3
Rush, J.4
Waechter, C.J.5
Raymond, K.M.6
Willer, T.7
Campbell, K.P.8
Freeze, H.H.9
Mehta, L.10
-
71
-
-
0034213178
-
Human dolichol-phosphate-mannose synthase consists of three subunits, DPM1, DPM2 and DPM3
-
Maeda, Y., Tanaka, S., Hino, J., Kangawa, K., and Kinoshita, T. (2000) Human dolichol-phosphate-mannose synthase consists of three subunits, DPM1, DPM2 and DPM3. EMBO J. 19, 2475-2482
-
(2000)
EMBO J.
, vol.19
, pp. 2475-2482
-
-
Maeda, Y.1
Tanaka, S.2
Hino, J.3
Kangawa, K.4
Kinoshita, T.5
-
72
-
-
84867904131
-
DPM2-CDG: A muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy
-
Barone, R., Aiello, C., Race, V., Morava, E., Foulquier, F., Riemersma, M., Passarelli, C., Concolino, D., Carella, M., Santorelli, F., Vleugels, W., Mercuri, E., Garozzo, D., Sturiale, L., Messina, S., Jaeken, J., Fiumara, A., Wevers, R.A., Bertini, E., Matthijs, G., and Lefeber, D.J. (2012) DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy. Ann. Neurol. 72, 550-558
-
(2012)
Ann. Neurol.
, vol.72
, pp. 550-558
-
-
Barone, R.1
Aiello, C.2
Race, V.3
Morava, E.4
Foulquier, F.5
Riemersma, M.6
Passarelli, C.7
Concolino, D.8
Carella, M.9
Santorelli, F.10
Vleugels, W.11
Mercuri, E.12
Garozzo, D.13
Sturiale, L.14
Messina, S.15
Jaeken, J.16
Fiumara, A.17
Wevers, R.A.18
Bertini, E.19
Matthijs, G.20
Lefeber, D.J.21
more..
-
73
-
-
67649584051
-
Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies
-
Lefeber, D.J., Schonberger, J., Morava, E., Guillard, M., Huyben, K.M., Verrijp, K., Grafakou, O., Evangeliou, A., Preijers, F.W., Manta, P., Yildiz, J., Grunewald, S., Spilioti, M., van den Elzen, C., Klein, D., Hess, D., Ashida, H., Hofsteenge, J., Maeda, Y., van den Heuvel, L., Lammens, M., Lehle, L., and Wevers, R.A. (2009) Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies. Am. J. Hum. Genet. 85, 76-86
-
(2009)
Am. J. Hum. Genet
, vol.85
, pp. 76-86
-
-
Lefeber, D.J.1
Schonberger, J.2
Morava, E.3
Guillard, M.4
Huyben, K.M.5
Verrijp, K.6
Grafakou, O.7
Evangeliou, A.8
Preijers, F.W.9
Manta, P.10
Yildiz, J.11
Grunewald, S.12
Spilioti, M.13
Van Den Elzen, C.14
Klein, D.15
Hess, D.16
Ashida, H.17
Hofsteenge, J.18
Maeda, Y.19
Van Den Heuvel, L.20
Lammens, M.21
Lehle, L.22
Wevers, R.A.23
more..
-
74
-
-
84855283452
-
Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation
-
Lefeber, D.J., de Brouwer, A.P., Morava, E., Riemersma, M., Schuurs-Hoeijmakers, J.H., Absmanner, B., Verrijp, K., van den Akker, W.M., Huijben, K., Steenbergen, G., van Reeuwijk, J., Jozwiak, A., Zucker, N., Lorber, A., Lammens, M., Knopf, C., van Bokhoven, H., Grunewald, S., Lehle, L., Kapusta, L., Mandel, H., and Wevers, R.A. (2011) Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation. PLoS Genet. 7, e1002427
-
(2011)
PLoS Genet
, vol.7
, pp. e1002427
-
-
Lefeber, D.J.1
De Brouwer, A.P.2
Morava, E.3
Riemersma, M.4
Schuurs-Hoeijmakers, J.H.5
Absmanner, B.6
Verrijp, K.7
Van Den Akker, W.M.8
Huijben, K.9
Steenbergen, G.10
Van Reeuwijk, J.11
Jozwiak, A.12
Zucker, N.13
Lorber, A.14
Lammens, M.15
Knopf, C.16
Van Bokhoven, H.17
Grunewald, S.18
Lehle, L.19
Kapusta, L.20
Mandel, H.21
Wevers, R.A.22
more..
-
75
-
-
0036744488
-
Expression and characterization of a human cDNA that complements the temperaturesensitive defect in dolichol kinase activity in the yeast sec59-1 mutant: The enzymatic phosphorylation of dolichol and diacylglycerol are catalyzed by separate CTPmediated kinase activities in Saccharomyces cerevisiae
-
Fernandez, F., Shridas, P., Jiang, S., Aebi, M., and Waechter, C.J. (2002) Expression and characterization of a human cDNA that complements the temperaturesensitive defect in dolichol kinase activity in the yeast sec59-1 mutant: the enzymatic phosphorylation of dolichol and diacylglycerol are catalyzed by separate CTPmediated kinase activities in Saccharomyces cerevisiae. Glycobiology 12, 555-562
-
(2002)
Glycobiology
, vol.12
, pp. 555-562
-
-
Fernandez, F.1
Shridas, P.2
Jiang, S.3
Aebi, M.4
Waechter, C.J.5
-
76
-
-
84860348118
-
ISPD lossof-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., Muntoni, F., Loder, A.S., Dobyns, W.B., Winder, T.L., Strahl, S., Mathews, K.D., Nelson, S.F., Moore, S.A., and Campbell, K.P. (2012) ISPD lossof-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
Muntoni, F.11
Loder, A.S.12
Dobyns, W.B.13
Winder, T.L.14
Strahl, S.15
Mathews, K.D.16
Nelson, S.F.17
Moore, S.A.18
Campbell, K.P.19
-
77
-
-
84860322514
-
Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of alphadystroglycan
-
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., Schraders, M., Altunoglu, U., Buckley, M.F., Brunner, H.G., Grisart, B., Zhou, H., Veltman, J.A., Gilissen, C., Mancini, G.M., Delree, P., Willemsen, M.A., Ramadza, D.P., Chitayat, D., Bennett, C., Sheridan, E., Peeters, E.A., Tan-Sindhunata, G.M., de Die-Smulders, C.E., Devriendt, K., Kayserili, H., El-Hashash, O.A., Stemple, D.L., Lefeber, D.J., Lin, Y.Y., and van Bokhoven, H. (2012) Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of alphadystroglycan. 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
Schraders, M.11
Altunoglu, U.12
Buckley, M.F.13
Brunner, H.G.14
Grisart, B.15
Zhou, H.16
Veltman, J.A.17
Gilissen, C.18
Mancini, G.M.19
Delree, P.20
Willemsen, M.A.21
Ramadza, D.P.22
Chitayat, D.23
Bennett, C.24
Sheridan, E.25
Peeters, E.A.26
Tan-Sindhunata, G.M.27
De Die-Smulders, C.E.28
Devriendt, K.29
Kayserili, H.30
El-Hashash, O.A.31
Stemple, D.L.32
Lefeber, D.J.33
Lin, Y.Y.34
Van Bokhoven, H.35
more..
-
78
-
-
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., Kunz, S., Oldstone, M.B., Accardi, A., Talim, B., Muntoni, F., Topaloglu, H., Dincer, P., and Campbell, K.P. (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
Kunz, S.11
Oldstone, M.B.12
Accardi, A.13
Talim, B.14
Muntoni, F.15
Topaloglu, H.16
Dincer, P.17
Campbell, K.P.18
-
79
-
-
38749138169
-
Protein O-mannosyltransferase activities in lymphoblasts from patients with alpha-dystroglycanopathies
-
Manya, H., Bouchet, C., Yanagisawa, A., Vuillaumier-Barrot, S., Quijano-Roy, S., Suzuki, Y., Maugenre, S., Richard, P., Inazu, T., Merlini, L., Romero, N.B., Leturcq, F., Bezier, I., Topaloglu, H., Estournet, B., Seta, N., Endo, T., and Guicheney, P. (2008) Protein O-mannosyltransferase activities in lymphoblasts from patients with alpha-dystroglycanopathies. Neuromuscul. Disord. 18, 45-51
-
(2008)
Neuromuscul. Disord.
, vol.18
, pp. 45-51
-
-
Manya, H.1
Bouchet, C.2
Yanagisawa, A.3
Vuillaumier-Barrot, S.4
Quijano-Roy, S.5
Suzuki, Y.6
Maugenre, S.7
Richard, P.8
Inazu, T.9
Merlini, L.10
Romero, N.B.11
Leturcq, F.12
Bezier, I.13
Topaloglu, H.14
Estournet, B.15
Seta, N.16
Endo, T.17
Guicheney, P.18
-
80
-
-
7444229243
-
Mutations of the POMT1 gene found in patients with Walker-Warburg syndrome lead to a defect of protein O-mannosylation
-
Akasaka-Manya, K., Manya, H., and Endo, T. (2004) Mutations of the POMT1 gene found in patients with Walker-Warburg syndrome lead to a defect of protein O-mannosylation. Biochem. Biophys. Res. Commun. 325, 75-79
-
(2004)
Biochem. Biophys. Res. Commun.
, vol.325
, pp. 75-79
-
-
Akasaka-Manya, K.1
Manya, H.2
Endo, T.3
-
81
-
-
67749098053
-
Tumor suppressor function of laminin-binding alpha-dystroglycan requires a distinct beta3-N-acetylglucosaminyltransferase
-
Bao, X., Kobayashi, M., Hatakeyama, S., Angata, K., Gullberg, D., Nakayama, J., Fukuda, M.N., and Fukuda, M. (2009) Tumor suppressor function of laminin-binding alpha-dystroglycan requires a distinct beta3-N-acetylglucosaminyltransferase. Proc. Natl. Acad. Sci. U.S.A. 106, 12109-12114
-
(2009)
Proc. Natl. Acad. Sci. U.S.A
, vol.106
, pp. 12109-12114
-
-
Bao, X.1
Kobayashi, M.2
Hatakeyama, S.3
Angata, K.4
Gullberg, D.5
Nakayama, J.6
Fukuda, M.N.7
Fukuda, M.8
-
82
-
-
84888068025
-
A truncating mutation in B3GNT1 causes severe Walker-Warburg syndrome
-
Shaheen, R., Faqeih, E., Ansari, S., and Alkuraya, F.S. (2013) A truncating mutation in B3GNT1 causes severe Walker-Warburg syndrome. Neurogenetics 14, 243-245
-
(2013)
Neurogenetics
, vol.14
, pp. 243-245
-
-
Shaheen, R.1
Faqeih, E.2
Ansari, S.3
Alkuraya, F.S.4
-
83
-
-
33750081100
-
Molecular interaction between fukutin and POMGnT1 in the glycosylation pathway of alpha-dystroglycan
-
Xiong, H., Kobayashi, K., Tachikawa, M., Manya, H., Takeda, S., Chiyonobu, T., Fujikake, N., Wang, F., Nishimoto, A., Morris, G.E., Nagai, Y., Kanagawa, M., Endo, T., and Toda, T. (2006) Molecular interaction between fukutin and POMGnT1 in the glycosylation pathway of alpha-dystroglycan. Biochem. Biophys. Res. Commun. 350, 935-941
-
(2006)
Biochem. Biophys. Res. Commun.
, vol.350
, pp. 935-941
-
-
Xiong, H.1
Kobayashi, K.2
Tachikawa, M.3
Manya, H.4
Takeda, S.5
Chiyonobu, T.6
Fujikake, N.7
Wang, F.8
Nishimoto, A.9
Morris, G.E.10
Nagai, Y.11
Kanagawa, M.12
Endo, T.13
Toda, T.14
|