-
1
-
-
68749120840
-
Mutational and functional analysis of Large in a novel CHO glycosylation mutant
-
Aguilan JT, Sundaram S, Nieves E, Stanley P. 2009. Mutational and functional analysis of Large in a novel CHO glycosylation mutant. Glycobiology. 19:971-986.
-
(2009)
Glycobiology.
, vol.19
, pp. 971-986
-
-
Aguilan, J.T.1
Sundaram, S.2
Nieves, E.3
Stanley, P.4
-
2
-
-
0033605915
-
Analysis of heparin, α-dystroglycan and sulfatide binding to the G domain of the laminin α1 chain by site-directed mutagenesis
-
DOI 10.1006/jmbi.1999.2606
-
Andac Z, Sasaki T, Mann K, Brancaccio A, Deutzmann R, Timpl R. 1999. Analysis of heparin, alpha-dystroglycan and sulfatide binding to the G domain of the laminin alpha1 chain by site-directed mutagenesis. J Mol Biol. 287:253-264. (Pubitemid 29141285)
-
(1999)
Journal of Molecular Biology
, vol.287
, Issue.2
, pp. 253-264
-
-
Andac, Z.1
Sasaki, T.2
Mann, K.3
Brancaccio, A.4
Deutzmann, R.5
Timpl, R.6
-
3
-
-
22844449331
-
The human solute carrier gene SLC35B4 encodes a bifunctional nucleotide sugar transporter with specificity for UDP-xylose and UDP-N-acetylglucosamine
-
DOI 10.1074/jbc.M504783200
-
Ashikov A, Routier F, Fuhlrott J, Helmus Y, Wild M, Gerardy-Schahn R, Bakker H. 2005. The human solute carrier gene SLC35B4 encodes a bifunctional nucleotide sugar transporter with specificity for UDP-xylose and UDP-N-acetylglucosamine. J Biol Chem. 280:27230-27235. (Pubitemid 41040762)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.29
, pp. 27230-27235
-
-
Ashikov, A.1
Routier, F.2
Fuhlrott, J.3
Helmus, Y.4
Wild, M.5
Gerardy-Schahn, R.6
Bakker, H.7
-
4
-
-
0030721537
-
Expression cloning of a cDNA encoding a sulfotransferase involved in the biosynthesis of the HNK-1 carbohydrate epitope
-
DOI 10.1074/jbc.272.47.29942
-
Bakker H, Friedmann I, Oka S, Kawasaki T, Nifant'ev N, Schachner M, Mantei N. 1997. Expression cloning of a cDNA encoding a sulfotransferase involved in the biosynthesis of the HNK-1 carbohydrate epitope. J Biol Chem. 272:29942-29946. (Pubitemid 27508096)
-
(1997)
Journal of Biological Chemistry
, vol.272
, Issue.47
, pp. 29942-29946
-
-
Bakker, H.1
Friedmann, I.2
Oka, S.3
Kawasaki, T.4
Nifant'Ev, N.5
Schachnerfl, M.6
Mantei, N.7
-
5
-
-
59049092970
-
Functional UDP-xylose transport across the endoplasmic reticulum/Golgi membrane in a Chinese hamster ovary cell mutant defective in UDP-xylose Synthase
-
Bakker H, Oka T, Ashikov A, Yadav A, Berger M, Rana NA, Bai X, Jigami Y, Haltiwanger RS, Esko JD, Gerardy-Schahn R. 2009. Functional UDP-xylose transport across the endoplasmic reticulum/Golgi membrane in a Chinese hamster ovary cell mutant defective in UDP-xylose Synthase. J Biol Chem. 284:2576-2583.
-
(2009)
J Biol Chem.
, vol.284
, pp. 2576-2583
-
-
Bakker, H.1
Oka, T.2
Ashikov, A.3
Yadav, A.4
Berger, M.5
Rana, N.A.6
Bai, X.7
Jigami, Y.8
Haltiwanger, R.S.9
Esko, J.D.10
Gerardy-Schahn, R.11
-
6
-
-
3142731311
-
LARGE can functionally bypass α-dystroglycan glycosylation defects in distinct congenital muscular dystrophies
-
DOI 10.1038/nm1059
-
Barresi R, Michele DE, Kanagawa M, Harper HA, Dovico SA, Satz JS, Moore SA, Zhang W, Schachter H, Dumanski JP, Cohn RD, Nishino I, Campbell KP. 2004. LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies. Nat Med. 10:696-703. (Pubitemid 38937634)
-
(2004)
Nature Medicine
, vol.10
, Issue.7
, pp. 696-703
-
-
Barresi, R.1
Michele, D.E.2
Kanagawa, M.3
Harper, H.A.4
Dovico, S.A.5
Satz, J.S.6
Moore, S.A.7
Zhang, W.8
Schachter, H.9
Dumanski, J.P.10
Cohn, R.D.11
Nishino, I.12
Campbell, K.P.13
-
7
-
-
0025815479
-
Membrane organization of the dystrophinglycoprotein complex
-
Ervasti JM, Campbell KP. 1991. Membrane organization of the dystrophinglycoprotein complex. Cell. 66:1121-1131.
-
(1991)
Cell.
, vol.66
, pp. 1121-1131
-
-
Ervasti, J.M.1
Campbell, K.P.2
-
8
-
-
14844299322
-
LARGE2 facilitates the maturation of α-dystroglycan more effectively than LARGE
-
DOI 10.1016/j.bbrc.2005.02.082
-
Fujimura K, Sawaki H, Sakai T, Hiruma T, Nakanishi N, Sato T, Ohkura T, Narimatsu H. 2005. LARGE2 facilitates the maturation of alphadystroglycan more effectively than LARGE. Biochem Biophys Res Commun. 329:1162-1171. (Pubitemid 40341397)
-
(2005)
Biochemical and Biophysical Research Communications
, vol.329
, Issue.3
, pp. 1162-1171
-
-
Fujimura, K.1
Sawaki, H.2
Sakai, T.3
Hiruma, T.4
Nakanishi, N.5
Sato, T.6
Ohkura, T.7
Narimatsu, H.8
-
10
-
-
0034975777
-
Mutant glycosyltransferase and altered glycosylation of α-dystroglycan in the myodystrophy mouse
-
DOI 10.1038/88865
-
Grewal PK, Holzfeind PJ, Bittner RE, Hewitt JE. 2001. Mutant glycosyltransferase and altered glycosylation of alpha-dystroglycan in the myodystrophy mouse. Nat Genet. 28:151-154. (Pubitemid 32538060)
-
(2001)
Nature Genetics
, vol.28
, Issue.2
, pp. 151-154
-
-
Grewal, P.K.1
Holzfeind, P.J.2
Bittner, R.E.3
Hewitt, J.E.4
-
11
-
-
27244440999
-
Characterization of the LARGE family of putative glycosyltransferases associated with dystroglycanopathies
-
DOI 10.1093/glycob/cwi094
-
Grewal PK, McLaughlan JM, Moore CJ, Browning CA, Hewitt JE. 2005. Characterization of the LARGE family of putative glycosyltransferases associated with dystroglycanopathies. Glycobiology. 15:912-923. (Pubitemid 41511487)
-
(2005)
Glycobiology
, vol.15
, Issue.10
, pp. 912-923
-
-
Grewal, P.K.1
McLaughlan, J.M.2
Moore, C.J.3
Browning, C.A.4
Hewitt, J.E.5
-
12
-
-
79951782427
-
Large induces functional glycans in an O-mannosylation dependent manner and targets GlcNAc terminals on alpha-dystroglycan
-
Hu Y, Li ZF, Wu X, Lu Q. 2011. Large induces functional glycans in an O-mannosylation dependent manner and targets GlcNAc terminals on alpha-dystroglycan. PLoS One. 6:e16866.
-
(2011)
PLoS One.
, vol.6
-
-
Hu, Y.1
Li, Z.F.2
Wu, X.3
Lu, Q.4
-
13
-
-
84855515852
-
Dystroglycan function requires xylosyl-and glucuronyltransferase activities of LARGE
-
Inamori K, Yoshida-Moriguchi T, Hara Y, Anderson ME, Yu L, Campbell KP. 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
-
14
-
-
2942733346
-
Molecular recognition by LARGE is essential for expression of functional dystroglycan
-
DOI 10.1016/j.cell.2004.06.003, PII S0092867404005434
-
Kanagawa M, Saito F, Kunz S, Yoshida-Moriguchi T, Barresi R, Kobayashi YM, Muschler J, Dumanski JP, Michele DE, Oldstone MB, Campbell KP. 2004. Molecular recognition by LARGE is essential for expression of functional dystroglycan. Cell. 117:953-964. (Pubitemid 38798860)
-
(2004)
Cell
, vol.117
, Issue.7
, 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.A.10
Campbell, K.P.11
-
15
-
-
0033657768
-
Complex carbohydrate synthesis tools for glycobiologists: Enzyme-based approach and programmable one-pot strategies
-
Koeller KM, Wong CH. 2000. Complex carbohydrate synthesis tools for glycobiologists: Enzyme-based approach and programmable one-pot strategies. Glycobiology. 10:1157-1169.
-
(2000)
Glycobiology.
, vol.10
, pp. 1157-1169
-
-
Koeller, K.M.1
Wong, C.H.2
-
16
-
-
10744226857
-
Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of α-dystroglycan
-
DOI 10.1093/hmg/ddg307
-
Longman C, Brockington M, Torelli S, Jimenez-Mallebrera C, Kennedy C, Khalil N, Feng L, Saran RK, Voit T, Merlini L, Sewry CA, Brown SC, 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. (Pubitemid 37407122)
-
(2003)
Human Molecular Genetics
, vol.12
, Issue.21
, 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
-
17
-
-
0038182574
-
Dystrophin-glycoprotein complex: Post-translational processing and dystroglycan function
-
DOI 10.1074/jbc.R200031200
-
Michele DE, Campbell KP. 2003. Dystrophin-glycoprotein complex: Post-translational processing and dystroglycan function. J Biol Chem. 278:15457-15460. (Pubitemid 36799650)
-
(2003)
Journal of Biological Chemistry
, vol.278
, Issue.18
, pp. 15457-15460
-
-
Michele, D.E.1
Campbell, K.P.2
-
18
-
-
62449178402
-
Dystroglycan glycosylation and muscular dystrophy
-
Moore CJ, Hewitt JE. 2009. Dystroglycan glycosylation and muscular dystrophy. Glycoconj J. 26:349-357.
-
(2009)
Glycoconj J.
, vol.26
, pp. 349-357
-
-
Moore, C.J.1
Hewitt, J.E.2
-
19
-
-
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. 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
-
20
-
-
0030026572
-
Differential heparin inhibition of skeletal muscle α-dystroglycan binding to laminins
-
DOI 10.1074/jbc.271.7.3817
-
Pall EA, Bolton KM, Ervasti JM. 1996. Differential heparin inhibition of skeletal muscle alpha-dystroglycan binding to laminins. J Biol Chem. 271:3817-3821. (Pubitemid 26069683)
-
(1996)
Journal of Biological Chemistry
, vol.271
, Issue.7
, pp. 3817-3821
-
-
Pall, E.A.1
Bolton, K.M.2
Ervasti, J.M.3
-
21
-
-
20144366896
-
Mouse large can modify complex N- and mucin O-glycans on α-dystroglycan to induce laminin binding
-
DOI 10.1074/jbc.M500069200
-
Patnaik SK, Stanley P. 2005. Mouse large can modify complex N-and mucin O-glycans on alpha-dystroglycan to induce laminin binding. J Biol Chem. 280:20851-20859. (Pubitemid 40776790)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.21
, pp. 20851-20859
-
-
Patnaik, S.K.1
Stanley, P.2
-
22
-
-
84856070820
-
Molecular cloning of a xylosyltransferase that transfers the second xylose to O-glucosylated epidermal growth factor repeats of notch
-
Sethi MK, Buettner FF, Ashikov A, Krylov VB, Takeuchi H, Nifantiev NE, Haltiwanger RS, Gerardy-Schahn R, Bakker H. 2012. Molecular cloning of a xylosyltransferase that transfers the second xylose to O-glucosylated epidermal growth factor repeats of notch. J Biol Chem. 287:2739-2748.
-
(2012)
J Biol Chem.
, vol.287
, pp. 2739-2748
-
-
Sethi, M.K.1
Buettner, F.F.2
Ashikov, A.3
Krylov, V.B.4
Takeuchi, H.5
Nifantiev, N.E.6
Haltiwanger, R.S.7
Gerardy-Schahn, R.8
Bakker, H.9
-
23
-
-
76249087224
-
Identification of glycosyltransferase 8 family members as xylosyltransferases acting on O-glucosylated notch epidermal growth factor repeats
-
Sethi MK, Buettner FF, Krylov VB, Takeuchi H, Nifantiev NE, Haltiwanger RS, Gerardy-Schahn R, Bakker H. 2010. Identification of glycosyltransferase 8 family members as xylosyltransferases acting on O-glucosylated notch epidermal growth factor repeats. J Biol Chem. 285:1582-1586.
-
(2010)
J Biol Chem.
, vol.285
, pp. 1582-1586
-
-
Sethi, M.K.1
Buettner, F.F.2
Krylov, V.B.3
Takeuchi, H.4
Nifantiev, N.E.5
Haltiwanger, R.S.6
Gerardy-Schahn, R.7
Bakker, H.8
-
24
-
-
33745885289
-
Tyramide signal amplification for DNA and mRNA in situ hybridization
-
Speel EJ, Hopman AH, Komminoth P. 2006. Tyramide signal amplification for DNA and mRNA in situ hybridization. Methods Mol Biol. 326:33-60.
-
(2006)
Methods Mol Biol.
, vol.326
, pp. 33-60
-
-
Speel, E.J.1
Hopman, A.H.2
Komminoth, P.3
-
25
-
-
80053572638
-
Mammalian O-mannosylation: Unsolved questions of structure/function
-
Stalnaker SH, Stuart R, Wells L. 2011. Mammalian O-mannosylation: Unsolved questions of structure/function. Curr Opin Struct Biol. 21:603-609.
-
(2011)
Curr Opin Struct Biol.
, vol.21
, pp. 603-609
-
-
Stalnaker, S.H.1
Stuart, R.2
Wells, L.3
-
26
-
-
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 DB, Venzke D, Cirak S, Schachter H, Vajsar J, Voit T, Muntoni F, Loder AS, Dobyns WB, Winder TL, Strahl S, Mathews KD, Nelson SF, Moore SA, Campbell KP. 2012. ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome. Nat Genet. 44:575-580.
-
(2012)
Nat Genet.
, vol.44
, pp. 575-580
-
-
Willer, T.1
Lee, H.2
Lommel, M.3
Yoshida-Moriguchi, T.4
De Bernabe, D.B.5
Venzke, D.6
Cirak, S.7
Schachter, H.8
Vajsar, J.9
Voit, T.10
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
-
27
-
-
74849131820
-
O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding
-
Yoshida-Moriguchi T, Yu L, Stalnaker SH, Davis S, Kunz S, Madson M, Oldstone MB, Schachter H, Wells L, Campbell KP. 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
-
28
-
-
84855889400
-
Differential glycosylation of alpha-dystroglycan and proteins other than alpha-dystroglycan by like-glycosyltransferase
-
Zhang P, Hu H. 2012. Differential glycosylation of alpha-dystroglycan and proteins other than alpha-dystroglycan by like-glycosyltransferase. Glycobiology. 22:235-247.
-
(2012)
Glycobiology.
, vol.22
, pp. 235-247
-
-
Zhang, P.1
Hu, H.2
|