Detalhe da pesquisa
1.
Functional Consequences of Mannose and Asialoglycoprotein Receptor Ablation.
J Biol Chem
; 291(36): 18700-17, 2016 09 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27405760
2.
The glycan-specific sulfotransferase (R77W)GalNAc-4-ST1 putatively responsible for peeling skin syndrome has normal properties consistent with a simple sequence polymorphisim.
Glycobiology
; 27(5): 450-456, 2017 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28204496
3.
Modulation of mannose and asialoglycoprotein receptor expression determines glycoprotein hormone half-life at critical points in the reproductive cycle.
J Biol Chem
; 289(17): 12157-12167, 2014 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-24619407
4.
Molecular basis for protein-specific transfer of N-acetylgalactosamine to N-linked glycans by the glycosyltransferases ß1,4-N-acetylgalactosaminyl transferase 3 (ß4GalNAc-T3) and ß4GalNAc-T4.
J Biol Chem
; 287(34): 29194-203, 2012 Aug 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-22722937
5.
Peptide-specific transfer of N-acetylgalactosamine to O-linked glycans by the glycosyltransferases ß1,4-N-acetylgalactosaminyl transferase 3 (ß4GalNAc-T3) and ß4GalNAc-T4.
J Biol Chem
; 287(34): 29204-12, 2012 Aug 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-22722940
6.
Loss of dermatan-4-sulfotransferase 1 function results in adducted thumb-clubfoot syndrome.
Am J Hum Genet
; 85(6): 873-82, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20004762
7.
Not so sweet malignant transformation.
Proc Natl Acad Sci U S A
; 111(39): 14009-10, 2014 Sep 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-25228771
8.
Ablation of GalNAc-4-sulfotransferase-1 enhances reproduction by altering the carbohydrate structures of luteinizing hormone in mice.
J Clin Invest
; 118(5): 1815-24, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18431515
9.
O-mannosylation of cadherins.
Proc Natl Acad Sci U S A
; 110(52): 20858-9, 2013 Dec 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-24344310
10.
Moving the O-glycoproteome from form to function.
Proc Natl Acad Sci U S A
; 109(25): 9672-3, 2012 Jun 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-22660927
11.
Regulation of lutropin circulatory half-life by the mannose/N-acetylgalactosamine-4-SO4 receptor is critical for implantation in vivo.
J Clin Invest
; 109(2): 269-76, 2002 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-11805139
12.
Loss of dermatan-4-sulfotransferase 1 (D4ST1/CHST14) function represents the first dermatan sulfate biosynthesis defect, "dermatan sulfate-deficient adducted thumb-clubfoot syndrome".
Hum Mutat
; 32(4): 484-5, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21309034
13.
Congenital disorders of glycosylation with emphasis on loss of dermatan-4-sulfotransferase.
Prog Mol Biol Transl Sci
; 93: 289-307, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20807649
14.
The Man/GalNAc-4-SO4-receptor: relating specificity to function.
Methods Enzymol
; 363: 121-33, 2003.
Artigo
em Inglês
| MEDLINE | ID: mdl-14579572
15.
The asialoglycoprotein receptor regulates levels of plasma glycoproteins terminating with sialic acid alpha2,6-galactose.
J Biol Chem
; 284(6): 3777-83, 2009 Feb 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-19075021
16.
A necessary and sufficient determinant for protein-selective glycosylation in vivo.
J Biol Chem
; 283(4): 1985-91, 2008 Jan 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-18048353
17.
N-linked oligosaccharides on the low density lipoprotein receptor homolog SorLA/LR11 are modified with terminal GalNAc-4-SO4 in kidney and brain.
J Biol Chem
; 282(3): 1873-81, 2007 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-17121844
18.
The asialoglycoprotein receptor clears glycoconjugates terminating with sialic acid alpha 2,6GalNAc.
Proc Natl Acad Sci U S A
; 102(47): 17125-9, 2005 Nov 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-16286643
19.
Differential expression and enzymatic properties of GalNAc-4-sulfotransferase-1 and GalNAc-4-sulfotransferase-2.
Glycobiology
; 15(12): 1349-58, 2005 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-16079414
20.
A major step on the road to understanding a unique posttranslational modification and its role in a genetic disease.
Cell
; 113(4): 421-2, 2003 May 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-12757700