-
1
-
-
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., Endo, T., 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 (1997), 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
-
2
-
-
84941114402
-
Glycobiology of alpha-dystroglycan and muscular dystrophy
-
Endo, T., Glycobiology of alpha-dystroglycan and muscular dystrophy. J. Biochem. 157 (2015), 1–12.
-
(2015)
J. Biochem.
, vol.157
, pp. 1-12
-
-
Endo, T.1
-
3
-
-
84995802648
-
O-mannosyl glycan and muscular dystrophy
-
T. Suzuki K. Ohtsubo N. Taniguchi Springer Japan Tokyo
-
Manya, H., Endo, T., O-mannosyl glycan and muscular dystrophy. Suzuki, T., Ohtsubo, K., Taniguchi, N., (eds.) Sugar Chains: Decoding the Functions of Glycans, 2015, Springer Japan, Tokyo, 235–258.
-
(2015)
Sugar Chains: Decoding the Functions of Glycans
, pp. 235-258
-
-
Manya, H.1
Endo, T.2
-
4
-
-
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., Feizi, T., 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 (1997), 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
-
5
-
-
0031790636
-
Detection of O-mannosyl glycans in rabbit skeletal muscle alpha-dystroglycan
-
Sasaki, T., Yamada, H., Matsumura, K., Shimizu, T., Kobata, A., Endo, T., Detection of O-mannosyl glycans in rabbit skeletal muscle alpha-dystroglycan. Biochim. Biophys. Acta 1425 (1998), 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
-
6
-
-
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., Endo, T., Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1. Dev. Cell 1 (2001), 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
-
7
-
-
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., Endo, T., Demonstration of mammalian protein O-mannosyltransferase activity: coexpression of POMT1 and POMT2 required for enzymatic activity. Proc. Natl. Acad. Sci. U. S. A. 101 (2004), 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
-
8
-
-
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., Brunner, H.G., Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome. Am. J. Hum. Genet. 71 (2002), 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
-
9
-
-
0038392675
-
Loss-of-function of an N-acetylglucosaminyltransferase, POMGnT1, in muscle-eye-brain disease
-
Manya, H., Sakai, K., Kobayashi, K., Taniguchi, K., Kawakita, M., Toda, T., Endo, T., Loss-of-function of an N-acetylglucosaminyltransferase, POMGnT1, in muscle-eye-brain disease. Biochem. Biophys. Res. Commun. 306 (2003), 93–97.
-
(2003)
Biochem. Biophys. Res. Commun.
, vol.306
, pp. 93-97
-
-
Manya, H.1
Sakai, K.2
Kobayashi, K.3
Taniguchi, K.4
Kawakita, M.5
Toda, T.6
Endo, T.7
-
10
-
-
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., van Bokhoven, H., POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome. J. Med. Genet. 42 (2005), 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
-
11
-
-
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., Guicheney, P., Protein O-mannosyltransferase activities in lymphoblasts from patients with alpha-dystroglycanopathies. Neuromuscul. Disord. 18 (2008), 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
-
12
-
-
0037010428
-
Defective glycosylation in muscular dystrophy
-
Muntoni, F., Brockington, M., Blake, D.J., Torelli, S., Brown, S.C., Defective glycosylation in muscular dystrophy. Lancet 360 (2002), 1419–1421.
-
(2002)
Lancet
, vol.360
, pp. 1419-1421
-
-
Muntoni, F.1
Brockington, M.2
Blake, D.J.3
Torelli, S.4
Brown, S.C.5
-
13
-
-
0038182574
-
Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function
-
Michele, D.E., Campbell, K.P., Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function. J. Biol. Chem. 278 (2003), 15457–15460.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 15457-15460
-
-
Michele, D.E.1
Campbell, K.P.2
-
14
-
-
0029063024
-
Electron microscopic evidence for a mucin-like region in chick muscle alpha-dystroglycan
-
Brancaccio, A., Schulthess, T., Gesemann, M., Engel, J., Electron microscopic evidence for a mucin-like region in chick muscle alpha-dystroglycan. FEBS Lett. 368 (1995), 139–142.
-
(1995)
FEBS Lett.
, vol.368
, pp. 139-142
-
-
Brancaccio, A.1
Schulthess, T.2
Gesemann, M.3
Engel, J.4
-
15
-
-
0029664729
-
Characterization of dystroglycan-laminin interaction in peripheral nerve
-
Yamada, H., Chiba, A., Endo, T., Kobata, A., Anderson, L.V., Hori, H., Fukuta-Ohi, H., Kanazawa, I., Campbell, K.P., Shimizu, T., Matsumura, K., Characterization of dystroglycan-laminin interaction in peripheral nerve. J. Neurochem. 66 (1996), 1518–1524.
-
(1996)
J. Neurochem.
, vol.66
, pp. 1518-1524
-
-
Yamada, H.1
Chiba, A.2
Endo, T.3
Kobata, A.4
Anderson, L.V.5
Hori, H.6
Fukuta-Ohi, H.7
Kanazawa, I.8
Campbell, K.P.9
Shimizu, T.10
Matsumura, K.11
-
16
-
-
0030916837
-
The N-terminal region of alpha-dystroglycan is an autonomous globular domain
-
Brancaccio, A., Schulthess, T., Gesemann, M., Engel, J., The N-terminal region of alpha-dystroglycan is an autonomous globular domain. Eur. J. Biochem. 246 (1997), 166–172.
-
(1997)
Eur. J. Biochem.
, vol.246
, pp. 166-172
-
-
Brancaccio, A.1
Schulthess, T.2
Gesemann, M.3
Engel, J.4
-
17
-
-
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., Campbell, K.P., Molecular recognition by LARGE is essential for expression of functional dystroglycan. Cell 117 (2004), 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
-
18
-
-
84960448786
-
Identification of a post-translational modification with Ribitol-phosphate and its defect in muscular dystrophy
-
Kanagawa, M., Kobayashi, K., Tajiri, M., Manya, H., Kuga, A., Yamaguchi, Y., Akasaka-Manya, K., Furukawa, J., Mizuno, M., Kawakami, H., Shinohara, Y., Wada, Y., Endo, T., Toda, T., Identification of a post-translational modification with Ribitol-phosphate and its defect in muscular dystrophy. Cell Rep. 14 (2016), 2209–2223.
-
(2016)
Cell Rep.
, vol.14
, pp. 2209-2223
-
-
Kanagawa, M.1
Kobayashi, K.2
Tajiri, M.3
Manya, H.4
Kuga, A.5
Yamaguchi, Y.6
Akasaka-Manya, K.7
Furukawa, J.8
Mizuno, M.9
Kawakami, H.10
Shinohara, Y.11
Wada, Y.12
Endo, T.13
Toda, T.14
-
19
-
-
85028716431
-
The muscular dystrophy gene TMEM5 encodes a ribitol beta1-4 Xylosyltransferase required for the functional glycosylation of dystroglycan
-
Manya, H., Yamaguchi, Y., Kanagawa, M., Kobayashi, K., Tajiri, M., Akasaka-Manya, K., Kawakami, H., Mizuno, M., Wada, Y., Toda, T., Endo, T., The muscular dystrophy gene TMEM5 encodes a ribitol beta1-4 Xylosyltransferase required for the functional glycosylation of dystroglycan. J. Biol. Chem. 161 (2016), 99–111.
-
(2016)
J. Biol. Chem.
, vol.161
, pp. 99-111
-
-
Manya, H.1
Yamaguchi, Y.2
Kanagawa, M.3
Kobayashi, K.4
Tajiri, M.5
Akasaka-Manya, K.6
Kawakami, H.7
Mizuno, M.8
Wada, Y.9
Toda, T.10
Endo, T.11
-
20
-
-
85047290208
-
Carbohydrate-binding domain of the POMGnT1 stem region modulates O-mannosylation sites of alpha-dystroglycan
-
Kuwabara, N., Manya, H., Yamada, T., Tateno, H., Kanagawa, M., Kobayashi, K., Akasaka-Manya, K., Hirose, Y., Mizuno, M., Ikeguchi, M., Toda, T., Hirabayashi, J., Senda, T., Endo, T., Kato, R., Carbohydrate-binding domain of the POMGnT1 stem region modulates O-mannosylation sites of alpha-dystroglycan. Proc. Natl. Acad. Sci. U. S. A. 113 (2016), 9280–9285.
-
(2016)
Proc. Natl. Acad. Sci. U. S. A.
, vol.113
, pp. 9280-9285
-
-
Kuwabara, N.1
Manya, H.2
Yamada, T.3
Tateno, H.4
Kanagawa, M.5
Kobayashi, K.6
Akasaka-Manya, K.7
Hirose, Y.8
Mizuno, M.9
Ikeguchi, M.10
Toda, T.11
Hirabayashi, J.12
Senda, T.13
Endo, T.14
Kato, R.15
-
21
-
-
0242322005
-
Molecular cloning and characterization of human GnT-IX, a novel beta1,6-N-acetylglucosaminyltransferase that is specifically expressed in the brain
-
Inamori, K., Endo, T., Ide, Y., Fujii, S., Gu, J., Honke, K., Taniguchi, N., Molecular cloning and characterization of human GnT-IX, a novel beta1,6-N-acetylglucosaminyltransferase that is specifically expressed in the brain. J. Biol. Chem. 278 (2003), 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
-
22
-
-
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., Pierce, M., A novel beta(1,6)-N-acetylglucosaminyltransferase V (GnT-VB)(1). FEBS Lett. 554 (2003), 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
-
23
-
-
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 O-mannosyl glycan
-
Inamori, K., Endo, T., Gu, J., Matsuo, I., Ito, Y., Fujii, S., Iwasaki, H., Narimatsu, H., Miyoshi, E., Honke, K., Taniguchi, N., N-Acetylglucosaminyltransferase IX acts on the GlcNAc beta 1,2-Man alpha 1-Ser/Thr moiety, forming a 2,6-branched structure in brain O-mannosyl glycan. J. Biol. Chem. 279 (2004), 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
-
24
-
-
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., Campbell, K.P., O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding. Science 327 (2010), 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
-
25
-
-
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., Strahl, S., Protein O-mannosylation is crucial for E-cadherin-mediated cell adhesion. Proc. Natl. Acad. Sci. U. S. A. 110 (2013), 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
-
26
-
-
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., Clausen, H., Mining the O-mannose glycoproteome reveals cadherins as major O-mannosylated glycoproteins. Proc. Natl. Acad. Sci. U. S. A. 110 (2013), 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
-
27
-
-
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., Endo, T., A new beta-1,2-N-acetylglucosaminyltransferase that may play a role in the biosynthesis of mammalian O-mannosyl glycans. Glycobiology 11 (2001), 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
-
28
-
-
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., Taniguchi, N., Loss of branched O-mannosyl glycans in astrocytes accelerates remyelination. J. Neurosci. 33 (2013), 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
-
29
-
-
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., Oka, S., Structural and biochemical characterization of O-mannose-linked human natural killer-1 glycan expressed on phosphacan in developing mouse brains. Glycobiology 24 (2014), 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
-
30
-
-
84941047569
-
Major glycan structure underlying expression of the Lewis X epitope in the developing brain is O-mannose-linked glycans on phosphacan/RPTPbeta
-
Yaji, S., Manya, H., Nakagawa, N., Takematsu, H., Endo, T., Kannagi, R., Yoshihara, T., Asano, M., Oka, S., Major glycan structure underlying expression of the Lewis X epitope in the developing brain is O-mannose-linked glycans on phosphacan/RPTPbeta. Glycobiology 25 (2015), 376–385.
-
(2015)
Glycobiology
, vol.25
, pp. 376-385
-
-
Yaji, S.1
Manya, H.2
Nakagawa, N.3
Takematsu, H.4
Endo, T.5
Kannagi, R.6
Yoshihara, T.7
Asano, M.8
Oka, S.9
-
31
-
-
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., Geyer, R., O-glycosylation pattern of CD24 from mouse brain. Biol. Chem. 390 (2009), 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
-
32
-
-
84864763681
-
RPTPzeta/phosphacan is abnormally glycosylated in a model of muscle-eye-brain disease lacking functional POMGnT1
-
Dwyer, C.A., Baker, E., Hu, H., Matthews, R.T., RPTPzeta/phosphacan is abnormally glycosylated in a model of muscle-eye-brain disease lacking functional POMGnT1. Neuroscience 220 (2012), 47–61.
-
(2012)
Neuroscience
, vol.220
, pp. 47-61
-
-
Dwyer, C.A.1
Baker, E.2
Hu, H.3
Matthews, R.T.4
-
33
-
-
84864578742
-
Neurofascin 186 is O-mannosylated within and outside of the mucin domain
-
Pacharra, S., Hanisch, F.G., Breloy, I., Neurofascin 186 is O-mannosylated within and outside of the mucin domain. J. Proteome Res. 11 (2012), 3955–3964.
-
(2012)
J. Proteome Res.
, vol.11
, pp. 3955-3964
-
-
Pacharra, S.1
Hanisch, F.G.2
Breloy, I.3
-
34
-
-
84875912842
-
The lecticans of mammalian brain perineural net are O-mannosylated
-
Pacharra, S., Hanisch, F.G., Muhlenhoff, M., Faissner, A., Rauch, U., Breloy, I., The lecticans of mammalian brain perineural net are O-mannosylated. J. Proteome Res. 12 (2013), 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
-
35
-
-
84865229984
-
Developmental expression of the neuron-specific N-acetylglucosaminyltransferase Vb (GnT-Vb/IX) and identification of its in vivo glycan products in comparison with those of its paralog, GnT-V
-
Lee, J.K., Matthews, R.T., Lim, J.M., Swanier, K., Wells, L., Pierce, J.M., Developmental expression of the neuron-specific N-acetylglucosaminyltransferase Vb (GnT-Vb/IX) and identification of its in vivo glycan products in comparison with those of its paralog, GnT-V. J. Biol. Chem. 287 (2012), 28526–28536.
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 28526-28536
-
-
Lee, J.K.1
Matthews, R.T.2
Lim, J.M.3
Swanier, K.4
Wells, L.5
Pierce, J.M.6
-
36
-
-
84995377287
-
Direct mapping of additional modifications on phosphorylated O-glycans of alpha-dystroglycan by mass spectrometry analysis in conjunction with knocking out of causative genes for dystroglycanopathy
-
Yagi, H., Kuo, C.W., Obayashi, T., Ninagawa, S., Khoo, K.H., Kato, K., Direct mapping of additional modifications on phosphorylated O-glycans of alpha-dystroglycan by mass spectrometry analysis in conjunction with knocking out of causative genes for dystroglycanopathy. Mol. Cell. Proteomics 15 (2016), 3424–3434.
-
(2016)
Mol. Cell. Proteomics
, vol.15
, pp. 3424-3434
-
-
Yagi, H.1
Kuo, C.W.2
Obayashi, T.3
Ninagawa, S.4
Khoo, K.H.5
Kato, K.6
-
37
-
-
84970998096
-
ISPD produces CDP-ribitol used by FKTN and FKRP to transfer ribitol phosphate onto alpha-dystroglycan
-
Gerin, I., Ury, B., Breloy, I., Bouchet-Seraphin, C., Bolsee, J., Halbout, M., Graff, J., Vertommen, D., Muccioli, G.G., Seta, N., Cuisset, J.M., Dabaj, I., Quijano-Roy, S., Grahn, A., Van Schaftingen, E., Bommer, G.T., ISPD produces CDP-ribitol used by FKTN and FKRP to transfer ribitol phosphate onto alpha-dystroglycan. Nat. Commun., 7, 2016, 11534.
-
(2016)
Nat. Commun.
, vol.7
, pp. 11534
-
-
Gerin, I.1
Ury, B.2
Breloy, I.3
Bouchet-Seraphin, C.4
Bolsee, J.5
Halbout, M.6
Graff, J.7
Vertommen, D.8
Muccioli, G.G.9
Seta, N.10
Cuisset, J.M.11
Dabaj, I.12
Quijano-Roy, S.13
Grahn, A.14
Van Schaftingen, E.15
Bommer, G.T.16
-
38
-
-
84979503456
-
The functional O-mannose glycan on alpha-dystroglycan contains a phospho-ribitol primed for matriglycan addition
-
Praissman, J.L., Willer, T., Sheikh, M.O., Toi, A., Chitayat, D., Lin, Y.Y., Lee, H., Stalnaker, S.H., Wang, S., Prabhakar, P.K., Nelson, S.F., Stemple, D.L., Moore, S.A., Moremen, K.W., Campbell, K.P., Wells, L., The functional O-mannose glycan on alpha-dystroglycan contains a phospho-ribitol primed for matriglycan addition. elife, 5, 2016, e14473.
-
(2016)
elife
, vol.5
-
-
Praissman, J.L.1
Willer, T.2
Sheikh, M.O.3
Toi, A.4
Chitayat, D.5
Lin, Y.Y.6
Lee, H.7
Stalnaker, S.H.8
Wang, S.9
Prabhakar, P.K.10
Nelson, S.F.11
Stemple, D.L.12
Moore, S.A.13
Moremen, K.W.14
Campbell, K.P.15
Wells, L.16
-
39
-
-
0027275643
-
A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin
-
Ervasti, J.M., Campbell, K.P., A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin. J. Cell Biol. 122 (1993), 809–823.
-
(1993)
J. Cell Biol.
, vol.122
, pp. 809-823
-
-
Ervasti, J.M.1
Campbell, K.P.2
-
40
-
-
0028321841
-
Identification and purification of an agrin receptor from Torpedo postsynaptic membranes: a heteromeric complex related to the dystroglycans
-
Bowe, M.A., Deyst, K.A., Leszyk, J.D., Fallon, J.R., Identification and purification of an agrin receptor from Torpedo postsynaptic membranes: a heteromeric complex related to the dystroglycans. Neuron 12 (1994), 1173–1180.
-
(1994)
Neuron
, vol.12
, pp. 1173-1180
-
-
Bowe, M.A.1
Deyst, K.A.2
Leszyk, J.D.3
Fallon, J.R.4
-
41
-
-
0028178082
-
Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor
-
Gee, S.H., Montanaro, F., Lindenbaum, M.H., Carbonetto, S., Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor. Cell 77 (1994), 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., Smalheiser, N.R., The relationship between perlecan and dystroglycan and its implication in the formation of the neuromuscular junction. Cell Adhes. Commun. 5 (1998), 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
-
-
0033557707
-
Binding of the G domains of laminin alpha1 and alpha2 chains and perlecan to heparin, sulfatides, alpha-dystroglycan and several extracellular matrix proteins
-
Talts, J.F., Andac, Z., Gohring, W., Brancaccio, A., Timpl, R., Binding of the G domains of laminin alpha1 and alpha2 chains and perlecan to heparin, sulfatides, alpha-dystroglycan and several extracellular matrix proteins. EMBO J. 18 (1999), 863–870.
-
(1999)
EMBO J.
, vol.18
, pp. 863-870
-
-
Talts, J.F.1
Andac, Z.2
Gohring, W.3
Brancaccio, A.4
Timpl, R.5
-
44
-
-
0035939672
-
A stoichiometric complex of neurexins and dystroglycan in brain
-
Sugita, S., Saito, F., Tang, J., Satz, J., Campbell, K., Sudhof, T.C., A stoichiometric complex of neurexins and dystroglycan in brain. J. Cell Biol. 154 (2001), 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
-
45
-
-
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., Furukawa, T., Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation. Nat. Neurosci. 11 (2008), 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
-
46
-
-
84872696903
-
Dystroglycan organizes axon guidance cue localization and axonal pathfinding
-
Wright, K.M., Lyon, K.A., Leung, H., Leahy, D.J., Ma, L., Ginty, D.D., Dystroglycan organizes axon guidance cue localization and axonal pathfinding. Neuron 76 (2012), 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
-
47
-
-
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., Straub, V., Mathews, K.D., Moore, S.A., Campbell, K.P., Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies. Nature 418 (2002), 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
Straub, V.11
Mathews, K.D.12
Moore, S.A.13
Campbell, K.P.14
-
48
-
-
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., Campbell, K.P., Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy. Nature 418 (2002), 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
-
49
-
-
33344477191
-
Aberrant glycosylation of alpha-dystroglycan and congenital muscular dystrophies
-
Endo, T., Aberrant glycosylation of alpha-dystroglycan and congenital muscular dystrophies. Acta Myol. 24 (2005), 64–69.
-
(2005)
Acta Myol.
, vol.24
, pp. 64-69
-
-
Endo, T.1
-
50
-
-
84982146215
-
Structural basis of laminin binding to the LARGE glycans on dystroglycan
-
Briggs, D.C., Yoshida-Moriguchi, T., Zheng, T., Venzke, D., Anderson, M.E., Strazzulli, A., Moracci, M., Yu, L., Hohenester, E., Campbell, K.P., Structural basis of laminin binding to the LARGE glycans on dystroglycan. Nat. Chem. Biol. 12 (2016), 810–814.
-
(2016)
Nat. Chem. Biol.
, vol.12
, pp. 810-814
-
-
Briggs, D.C.1
Yoshida-Moriguchi, T.2
Zheng, T.3
Venzke, D.4
Anderson, M.E.5
Strazzulli, A.6
Moracci, M.7
Yu, L.8
Hohenester, E.9
Campbell, K.P.10
-
51
-
-
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., Endo, T., Role of N-glycans in maintaining the activity of protein O-mannosyltransferases POMT1 and POMT2. J. Biochem. 147 (2010), 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
-
52
-
-
34547093904
-
Regulation of mammalian protein O-mannosylation: preferential amino acid sequence for O-mannose modification
-
Manya, H., Suzuki, T., Akasaka-Manya, K., Ishida, H.K., Mizuno, M., Suzuki, Y., Inazu, T., Dohmae, N., Endo, T., Regulation of mammalian protein O-mannosylation: preferential amino acid sequence for O-mannose modification. J. Biol. Chem. 282 (2007), 20200–20206.
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 20200-20206
-
-
Manya, H.1
Suzuki, T.2
Akasaka-Manya, K.3
Ishida, H.K.4
Mizuno, M.5
Suzuki, Y.6
Inazu, T.7
Dohmae, N.8
Endo, T.9
-
53
-
-
33745817404
-
Physical and functional association of human protein O-mannosyltransferases 1 and 2
-
Akasaka-Manya, K., Manya, H., Nakajima, A., Kawakita, M., Endo, T., Physical and functional association of human protein O-mannosyltransferases 1 and 2. J. Biol. Chem. 281 (2006), 19339–19345.
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 19339-19345
-
-
Akasaka-Manya, K.1
Manya, H.2
Nakajima, A.3
Kawakita, M.4
Endo, T.5
-
54
-
-
80051572425
-
Different roles of the two components of human protein O-mannosyltransferase, POMT1 and POMT2
-
Akasaka-Manya, K., Manya, H., Hayashi, M., Endo, T., Different roles of the two components of human protein O-mannosyltransferase, POMT1 and POMT2. Biochem. Biophys. Res. Commun. 411 (2011), 721–725.
-
(2011)
Biochem. Biophys. Res. Commun.
, vol.411
, pp. 721-725
-
-
Akasaka-Manya, K.1
Manya, H.2
Hayashi, M.3
Endo, T.4
-
55
-
-
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., Muntoni, F., Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of alpha-dystroglycan. Am. J. Hum. Genet. 93 (2013), 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..
-
56
-
-
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., Wevers, R.A., Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation. PLoS Genet., 7, 2011, e1002427.
-
(2011)
PLoS Genet.
, vol.7
-
-
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..
-
57
-
-
0034213178
-
Human dolichol-phosphate-mannose synthase consists of three subunits, DPM1, DPM2 and DPM3
-
Maeda, Y., Tanaka, S., Hino, J., Kangawa, K., Kinoshita, T., Human dolichol-phosphate-mannose synthase consists of three subunits, DPM1, DPM2 and DPM3. EMBO J. 19 (2000), 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
-
58
-
-
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., Wevers, R.A., Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies. Am. J. Hum. Genet. 85 (2009), 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..
-
59
-
-
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., Lefeber, D.J., DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy. Ann. Neurol. 72 (2012), 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..
-
60
-
-
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., Mehta, L., Congenital disorder of glycosylation due to DPM1 mutations presenting with dystroglycanopathy-type congenital muscular dystrophy. Mol. Genet. Metab. 110 (2013), 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
-
61
-
-
0030721537
-
Expression cloning of a cDNA encoding a sulfotransferase involved in the biosynthesis of the HNK-1 carbohydrate epitope
-
Bakker, H., Friedmann, I., Oka, S., Kawasaki, T., Nifant'ev, N., Schachner, M., Mantei, N., Expression cloning of a cDNA encoding a sulfotransferase involved in the biosynthesis of the HNK-1 carbohydrate epitope. J. Biol. Chem. 272 (1997), 29942–29946.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 29942-29946
-
-
Bakker, H.1
Friedmann, I.2
Oka, S.3
Kawasaki, T.4
Nifant'ev, N.5
Schachner, M.6
Mantei, N.7
-
62
-
-
0030911792
-
Cloning and functional expression of a novel glucuronyltransferase involved in the biosynthesis of the carbohydrate epitope HNK-1
-
Terayama, K., Oka, S., Seiki, T., Miki, Y., Nakamura, A., Kozutsumi, Y., Takio, K., Kawasaki, T., Cloning and functional expression of a novel glucuronyltransferase involved in the biosynthesis of the carbohydrate epitope HNK-1. Proc. Natl. Acad. Sci. U. S. A. 94 (1997), 6093–6098.
-
(1997)
Proc. Natl. Acad. Sci. U. S. A.
, vol.94
, pp. 6093-6098
-
-
Terayama, K.1
Oka, S.2
Seiki, T.3
Miki, Y.4
Nakamura, A.5
Kozutsumi, Y.6
Takio, K.7
Kawasaki, T.8
-
63
-
-
0032586973
-
Alpha1,3-fucosyltransferase IX (Fuc-TIX) is very highly conserved between human and mouse; molecular cloning, characterization and tissue distribution of human Fuc-TIX
-
Kaneko, M., Kudo, T., Iwasaki, H., Ikehara, Y., Nishihara, S., Nakagawa, S., Sasaki, K., Shiina, T., Inoko, H., Saitou, N., Narimatsu, H., Alpha1,3-fucosyltransferase IX (Fuc-TIX) is very highly conserved between human and mouse; molecular cloning, characterization and tissue distribution of human Fuc-TIX. FEBS Lett. 452 (1999), 237–242.
-
(1999)
FEBS Lett.
, vol.452
, pp. 237-242
-
-
Kaneko, M.1
Kudo, T.2
Iwasaki, H.3
Ikehara, Y.4
Nishihara, S.5
Nakagawa, S.6
Sasaki, K.7
Shiina, T.8
Inoko, H.9
Saitou, N.10
Narimatsu, H.11
-
64
-
-
0033525021
-
Molecular cloning and expression of a second glucuronyltransferase involved in the biosynthesis of the HNK-1 carbohydrate epitope
-
Seiki, T., Oka, S., Terayama, K., Imiya, K., Kawasaki, T., Molecular cloning and expression of a second glucuronyltransferase involved in the biosynthesis of the HNK-1 carbohydrate epitope. Biochem. Biophys. Res. Commun. 255 (1999), 182–187.
-
(1999)
Biochem. Biophys. Res. Commun.
, vol.255
, pp. 182-187
-
-
Seiki, T.1
Oka, S.2
Terayama, K.3
Imiya, K.4
Kawasaki, T.5
-
65
-
-
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., Nishihara, S., beta4GalT-II is a key regulator of glycosylation of the proteins involved in neuronal development. Biochem. Biophys. Res. Commun. 333 (2005), 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
-
66
-
-
33845588130
-
Mice lacking alpha1,3-fucosyltransferase IX demonstrate disappearance of Lewis x structure in brain and increased anxiety-like behaviors
-
Kudo, T., Fujii, T., Ikegami, S., Inokuchi, K., Takayama, Y., Ikehara, Y., Nishihara, S., Togayachi, A., Takahashi, S., Tachibana, K., Yuasa, S., Narimatsu, H., Mice lacking alpha1,3-fucosyltransferase IX demonstrate disappearance of Lewis x structure in brain and increased anxiety-like behaviors. Glycobiology 17 (2007), 1–9.
-
(2007)
Glycobiology
, vol.17
, pp. 1-9
-
-
Kudo, T.1
Fujii, T.2
Ikegami, S.3
Inokuchi, K.4
Takayama, Y.5
Ikehara, Y.6
Nishihara, S.7
Togayachi, A.8
Takahashi, S.9
Tachibana, K.10
Yuasa, S.11
Narimatsu, H.12
-
67
-
-
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., Oka, S., Human natural killer-1 sulfotransferase (HNK-1ST)-induced sulfate transfer regulates laminin-binding glycans on alpha-dystroglycan. J. Biol. Chem. 287 (2012), 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
-
68
-
-
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., Campbell, K.P., SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function. Science 341 (2013), 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
-
69
-
-
85012050403
-
Protein O-linked mannose beta-1,4-N-Acetylglucosaminyl-transferase 2 (POMGNT2) is a gatekeeper enzyme for functional glycosylation of alpha-Dystroglycan
-
Halmo, S.M., Singh, D., Patel, S., Wang, S., Edlin, M., Boons, G.J., Moremen, K.W., Live, D., Wells, L., Protein O-linked mannose beta-1,4-N-Acetylglucosaminyl-transferase 2 (POMGNT2) is a gatekeeper enzyme for functional glycosylation of alpha-Dystroglycan. J. Biol. Chem. 292 (2017), 2101–2109.
-
(2017)
J. Biol. Chem.
, vol.292
, pp. 2101-2109
-
-
Halmo, S.M.1
Singh, D.2
Patel, S.3
Wang, S.4
Edlin, M.5
Boons, G.J.6
Moremen, K.W.7
Live, D.8
Wells, L.9
-
70
-
-
85016162643
-
B4GAT1 is the priming enzyme for the LARGE-dependent functional glycosylation of alpha-dystroglycan
-
Praissman, J.L., Live, D.H., Wang, S., Ramiah, A., Chinoy, Z.S., Boons, G.J., Moremen, K.W., Wells, L., B4GAT1 is the priming enzyme for the LARGE-dependent functional glycosylation of alpha-dystroglycan. elife, 3, 2014, e03943.
-
(2014)
elife
, vol.3
-
-
Praissman, J.L.1
Live, D.H.2
Wang, S.3
Ramiah, A.4
Chinoy, Z.S.5
Boons, G.J.6
Moremen, K.W.7
Wells, L.8
-
71
-
-
85001799433
-
The glucuronyltransferase B4GAT1 is required for initiation of LARGE-mediated alpha-dystroglycan functional glycosylation
-
Willer, T., Inamori, K., Venzke, D., Harvey, C., Morgensen, G., Hara, Y., Beltran Valero de Bernabe, D., Yu, L., Wright, K.M., Campbell, K.P., The glucuronyltransferase B4GAT1 is required for initiation of LARGE-mediated alpha-dystroglycan functional glycosylation. elife, 3, 2014, e03941.
-
(2014)
elife
, vol.3
-
-
Willer, T.1
Inamori, K.2
Venzke, D.3
Harvey, C.4
Morgensen, G.5
Hara, Y.6
Beltran Valero de Bernabe, D.7
Yu, L.8
Wright, K.M.9
Campbell, K.P.10
-
72
-
-
84855515852
-
Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE
-
Inamori, K., Yoshida-Moriguchi, T., Hara, Y., Anderson, M.E., Yu, L., Campbell, K.P., Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE. Science 335 (2012), 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
-
73
-
-
84875730533
-
LARGE2 generates the same xylose- and glucuronic acid-containing glycan structures as LARGE
-
Ashikov, A., Buettner, F.F., Tiemann, B., Gerardy-Schahn, R., Bakker, H., LARGE2 generates the same xylose- and glucuronic acid-containing glycan structures as LARGE. Glycobiology 23 (2013), 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
-
74
-
-
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., Campbell, K.P., Xylosyl- and glucuronyltransferase functions of LARGE in alpha-dystroglycan modification are conserved in LARGE2. Glycobiology 23 (2013), 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
-
75
-
-
84999131369
-
LARGE2-dependent glycosylation confers laminin-binding ability on proteoglycans
-
Inamori, K.I., Beedle, A.M., de Bernabe, D.B., Wright, M.E., Campbell, K.P., LARGE2-dependent glycosylation confers laminin-binding ability on proteoglycans. Glycobiology 26 (2016), 1284–1296.
-
(2016)
Glycobiology
, vol.26
, pp. 1284-1296
-
-
Inamori, K.I.1
Beedle, A.M.2
de Bernabe, D.B.3
Wright, M.E.4
Campbell, K.P.5
-
76
-
-
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., Campbell, K.P., Like-acetylglucosaminyltransferase (LARGE)-dependent modification of dystroglycan at Thr-317/319 is required for laminin binding and arenavirus infection. Proc. Natl. Acad. Sci. U. S. A. 108 (2011), 17426–17431.
-
(2011)
Proc. Natl. Acad. Sci. U. S. A.
, 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
-
77
-
-
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., Campbell, K.P., A dystroglycan mutation associated with limb-girdle muscular dystrophy. N. Engl. J. Med. 364 (2011), 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
-
78
-
-
84884512916
-
Wall teichoic acids of gram-positive bacteria
-
Brown, S., Santa Maria, J.P. Jr., Walker, S., Wall teichoic acids of gram-positive bacteria. Annu. Rev. Microbiol. 67 (2013), 313–336.
-
(2013)
Annu. Rev. Microbiol.
, vol.67
, pp. 313-336
-
-
Brown, S.1
Santa Maria, J.P.2
Walker, S.3
-
79
-
-
84860322514
-
Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of alpha-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., 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., van Bokhoven, H., Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of alpha-dystroglycan. Nat. Genet. 44 (2012), 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..
-
80
-
-
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., Muntoni, F., Loder, A.S., Dobyns, W.B., Winder, T.L., Strahl, S., Mathews, K.D., Nelson, S.F., Moore, S.A., Campbell, K.P., ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome. Nat. Genet. 44 (2012), 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
-
81
-
-
84951569890
-
Human ISPD is a Cytidyltransferase required for Dystroglycan O-Mannosylation
-
Riemersma, M., Froese, D.S., van Tol, W., Engelke, U.F., Kopec, J., van Scherpenzeel, M., Ashikov, A., Krojer, T., von Delft, F., Tessari, M., Buczkowska, A., Swiezewska, E., Jae, L.T., Brummelkamp, T.R., Manya, H., Endo, T., van Bokhoven, H., Yue, W.W., Lefeber, D.J., Human ISPD is a Cytidyltransferase required for Dystroglycan O-Mannosylation. Chem. Biol. 22 (2015), 1643–1652.
-
(2015)
Chem. Biol.
, vol.22
, pp. 1643-1652
-
-
Riemersma, M.1
Froese, D.S.2
van Tol, W.3
Engelke, U.F.4
Kopec, J.5
van Scherpenzeel, M.6
Ashikov, A.7
Krojer, T.8
von Delft, F.9
Tessari, M.10
Buczkowska, A.11
Swiezewska, E.12
Jae, L.T.13
Brummelkamp, T.R.14
Manya, H.15
Endo, T.16
van Bokhoven, H.17
Yue, W.W.18
Lefeber, D.J.19
-
82
-
-
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., Toda, T., An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy. Nature 394 (1998), 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
-
83
-
-
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., Muntoni, F., 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 (2001), 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
-
84
-
-
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., Fallet, S., Romero, N., Fardeau, M., Straub, V., Storey, G., Pollitt, C., Richard, I., Sewry, C.A., Bushby, K., Voit, T., Blake, D.J., Muntoni, F., 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 (2001), 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..
-
85
-
-
0036291325
-
Deficiency of alpha-dystroglycan in muscle-eye-brain disease
-
Kano, H., Kobayashi, K., Herrmann, R., Tachikawa, M., Manya, H., Nishino, I., Nonaka, I., Straub, V., Talim, B., Voit, T., Topaloglu, H., Endo, T., Yoshikawa, H., Toda, T., Deficiency of alpha-dystroglycan in muscle-eye-brain disease. Biochem. Biophys. Res. Commun. 291 (2002), 1283–1286.
-
(2002)
Biochem. Biophys. Res. Commun.
, vol.291
, pp. 1283-1286
-
-
Kano, H.1
Kobayashi, K.2
Herrmann, R.3
Tachikawa, M.4
Manya, H.5
Nishino, I.6
Nonaka, I.7
Straub, V.8
Talim, B.9
Voit, T.10
Topaloglu, H.11
Endo, T.12
Yoshikawa, H.13
Toda, T.14
-
86
-
-
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., Endo, T., Structure-function analysis of human protein O-linked mannose b1,2-N-acetylglucosaminyltransferase 1, POMGnT1. Biochem. Biophys. Res. Commun. 320 (2004), 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
-
87
-
-
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., Toda, T., Molecular interaction between fukutin and POMGnT1 in the glycosylation pathway of alpha-dystroglycan. Biochem. Biophys. Res. Commun. 350 (2006), 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
-
88
-
-
84963739524
-
Mutations in POMGNT1 cause non-syndromic retinitis pigmentosa
-
Xu, M., Yamada, T., Sun, Z., Eblimit, A., Lopez, I., Wang, F., Manya, H., Xu, S., Zhao, L., Li, Y., Kimchi, A., Sharon, D., Sui, R., Endo, T., Koenekoop, R.K., Chen, R., Mutations in POMGNT1 cause non-syndromic retinitis pigmentosa. Hum. Mol. Genet. 25 (2016), 1479–1488.
-
(2016)
Hum. Mol. Genet.
, vol.25
, pp. 1479-1488
-
-
Xu, M.1
Yamada, T.2
Sun, Z.3
Eblimit, A.4
Lopez, I.5
Wang, F.6
Manya, H.7
Xu, S.8
Zhao, L.9
Li, Y.10
Kimchi, A.11
Sharon, D.12
Sui, R.13
Endo, T.14
Koenekoop, R.K.15
Chen, R.16
-
89
-
-
0034975777
-
Mutant glycosyltransferase and altered glycosylation of alpha-dystroglycan in the myodystrophy mouse
-
Grewal, P.K., Holzfeind, P.J., Bittner, R.E., Hewitt, J.E., Mutant glycosyltransferase and altered glycosylation of alpha-dystroglycan in the myodystrophy mouse. Nat. Genet. 28 (2001), 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
-
90
-
-
33645971589
-
A genetic model for muscle-eye-brain disease in mice lacking protein O-mannose 1,2-N-acetylglucosaminyltransferase (POMGnT1)
-
Liu, J., Ball, S.L., Yang, Y., Mei, P., Zhang, L., Shi, H., Kaminski, H.J., Lemmon, V.P., Hu, H., A genetic model for muscle-eye-brain disease in mice lacking protein O-mannose 1,2-N-acetylglucosaminyltransferase (POMGnT1). Mech. Dev. 123 (2006), 228–240.
-
(2006)
Mech. Dev.
, vol.123
, pp. 228-240
-
-
Liu, J.1
Ball, S.L.2
Yang, Y.3
Mei, P.4
Zhang, L.5
Shi, H.6
Kaminski, H.J.7
Lemmon, V.P.8
Hu, H.9
-
91
-
-
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., Pierce, M., Receptor tyrosine phosphatase beta (RPTPbeta) activity and signaling are attenuated by glycosylation and subsequent cell surface galectin-1 binding. J. Biol. Chem. 283 (2008), 33026–33035.
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 33026-33035
-
-
Abbott, K.L.1
Matthews, R.T.2
Pierce, M.3
-
92
-
-
71049182589
-
HNK-1 glyco-epitope regulates the stability of the glutamate receptor subunit GluR2 on the neuronal cell surface
-
Morita, I., Kakuda, S., Takeuchi, Y., Itoh, S., Kawasaki, N., Kizuka, Y., Kawasaki, T., Oka, S., HNK-1 glyco-epitope regulates the stability of the glutamate receptor subunit GluR2 on the neuronal cell surface. J. Biol. Chem. 284 (2009), 30209–30217.
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 30209-30217
-
-
Morita, I.1
Kakuda, S.2
Takeuchi, Y.3
Itoh, S.4
Kawasaki, N.5
Kizuka, Y.6
Kawasaki, T.7
Oka, S.8
-
93
-
-
70449526388
-
HNK-1 (human natural killer-1) glyco-epitope is essential for normal spine morphogenesis in developing hippocampal neurons
-
Morita, I., Kakuda, S., Takeuchi, Y., Kawasaki, T., Oka, S., HNK-1 (human natural killer-1) glyco-epitope is essential for normal spine morphogenesis in developing hippocampal neurons. Neuroscience 164 (2009), 1685–1694.
-
(2009)
Neuroscience
, vol.164
, pp. 1685-1694
-
-
Morita, I.1
Kakuda, S.2
Takeuchi, Y.3
Kawasaki, T.4
Oka, S.5
-
94
-
-
79955537997
-
Structurally distinct LewisX glycans distinguish subpopulations of neural stem/progenitor cells
-
Hennen, E., Czopka, T., Faissner, A., Structurally distinct LewisX glycans distinguish subpopulations of neural stem/progenitor cells. J. Biol. Chem. 286 (2011), 16321–16331.
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 16321-16331
-
-
Hennen, E.1
Czopka, T.2
Faissner, A.3
|