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Items: 1 to 20 of 210

1.

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.

PLoS One. 2011 Feb 9;6(2):e16866. doi: 10.1371/journal.pone.0016866.

2.

Mouse large can modify complex N- and mucin O-glycans on alpha-dystroglycan to induce laminin binding.

Patnaik SK, Stanley P.

J Biol Chem. 2005 May 27;280(21):20851-9. Epub 2005 Mar 23.

3.

Differential glycosylation of α-dystroglycan and proteins other than α-dystroglycan by like-glycosyltransferase.

Zhang P, Hu H.

Glycobiology. 2012 Feb;22(2):235-47. doi: 10.1093/glycob/cwr131. Epub 2011 Sep 19.

4.

Mammalian O-mannosylation of cadherins and plexins is independent of protein O-mannosyltransferases 1 and 2.

Larsen ISB, Narimatsu Y, Joshi HJ, Yang Z, Harrison OJ, Brasch J, Shapiro L, Honig B, Vakhrushev SY, Clausen H, Halim A.

J Biol Chem. 2017 Jul 7;292(27):11586-11598. doi: 10.1074/jbc.M117.794487. Epub 2017 May 16.

5.

[Recent Advances in α-dystroglycanopathy].

Kuga A, Kanagawa M, Toda T.

Brain Nerve. 2011 Nov;63(11):1189-95. Review. Japanese.

PMID:
22068471
6.

AGO61-dependent GlcNAc modification primes the formation of functional glycans on α-dystroglycan.

Yagi H, Nakagawa N, Saito T, Kiyonari H, Abe T, Toda T, Wu SW, Khoo KH, Oka S, Kato K.

Sci Rep. 2013 Nov 21;3:3288. doi: 10.1038/srep03288.

7.

GTDC2 modifies O-mannosylated α-dystroglycan in the endoplasmic reticulum to generate N-acetyl glucosamine epitopes reactive with CTD110.6 antibody.

Ogawa M, Nakamura N, Nakayama Y, Kurosaka A, Manya H, Kanagawa M, Endo T, Furukawa K, Okajima T.

Biochem Biophys Res Commun. 2013 Oct 11;440(1):88-93. doi: 10.1016/j.bbrc.2013.09.022. Epub 2013 Sep 13.

PMID:
24041696
8.

Mutational and functional analysis of Large in a novel CHO glycosylation mutant.

Aguilan JT, Sundaram S, Nieves E, Stanley P.

Glycobiology. 2009 Sep;19(9):971-86. doi: 10.1093/glycob/cwp074. Epub 2009 May 21.

9.

Small molecules enhance functional O-mannosylation of Alpha-dystroglycan.

Lv F, Li ZF, Hu W, Wu X.

Bioorg Med Chem. 2015 Dec 15;23(24):7661-70. doi: 10.1016/j.bmc.2015.11.011. Epub 2015 Nov 12.

PMID:
26652968
10.

Drosophila Dystroglycan is a target of O-mannosyltransferase activity of two protein O-mannosyltransferases, Rotated Abdomen and Twisted.

Nakamura N, Stalnaker SH, Lyalin D, Lavrova O, Wells L, Panin VM.

Glycobiology. 2010 Mar;20(3):381-94. doi: 10.1093/glycob/cwp189. Epub 2009 Dec 7.

11.

O Mannosylation of alpha-dystroglycan is essential for lymphocytic choriomeningitis virus receptor function.

Imperiali M, Thoma C, Pavoni E, Brancaccio A, Callewaert N, Oxenius A.

J Virol. 2005 Nov;79(22):14297-308.

12.

O-Mannose and O-N-acetyl galactosamine glycosylation of mammalian α-dystroglycan is conserved in a region-specific manner.

Gomez Toledo A, Raducu M, Cruces J, Nilsson J, Halim A, Larson G, Rüetschi U, Grahn A.

Glycobiology. 2012 Nov;22(11):1413-23. doi: 10.1093/glycob/cws109. Epub 2012 Jul 9.

PMID:
22781125
13.
14.

HNK-1 sulfotransferase-dependent sulfation regulating laminin-binding glycans occurs in the post-phosphoryl moiety on α-dystroglycan.

Nakagawa N, Takematsu H, Oka S.

Glycobiology. 2013 Sep;23(9):1066-74. doi: 10.1093/glycob/cwt043. Epub 2013 May 30.

15.

Glycomic analyses of mouse models of congenital muscular dystrophy.

Stalnaker SH, Aoki K, Lim JM, Porterfield M, Liu M, Satz JS, Buskirk S, Xiong Y, Zhang P, Campbell KP, Hu H, Live D, Tiemeyer M, Wells L.

J Biol Chem. 2011 Jun 17;286(24):21180-90. doi: 10.1074/jbc.M110.203281. Epub 2011 Apr 1.

16.

Human natural killer-1 sulfotransferase (HNK-1ST)-induced sulfate transfer regulates laminin-binding glycans on α-dystroglycan.

Nakagawa N, Manya H, Toda T, Endo T, Oka S.

J Biol Chem. 2012 Aug 31;287(36):30823-32. doi: 10.1074/jbc.M112.363036. Epub 2012 Jul 16.

17.

LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies.

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.

Nat Med. 2004 Jul;10(7):696-703. Epub 2004 Jun 6.

18.

Mammalian O-mannosylation: unsolved questions of structure/function.

Stalnaker SH, Stuart R, Wells L.

Curr Opin Struct Biol. 2011 Oct;21(5):603-9. doi: 10.1016/j.sbi.2011.09.001. Epub 2011 Sep 22. Review.

19.

Disease mutations in CMP-sialic acid transporter SLC35A1 result in abnormal α-dystroglycan O-mannosylation, independent from sialic acid.

Riemersma M, Sandrock J, Boltje TJ, Büll C, Heise T, Ashikov A, Adema GJ, van Bokhoven H, Lefeber DJ.

Hum Mol Genet. 2015 Apr 15;24(8):2241-6. doi: 10.1093/hmg/ddu742. Epub 2014 Dec 30.

PMID:
25552652

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