scholarly article | Q13442814 |
P50 | author | Liping Yu | Q55189535 |
Kevin P Campbell | Q58144660 | ||
Stanley F Nelson | Q90679187 | ||
Takako Yoshida-Moriguchi | Q105623621 | ||
P2093 | author name string | Mary E Anderson | |
Hane Lee | |||
Tobias Willer | |||
Francesco Muntoni | |||
David Venzke | |||
Tamieka Whyte | |||
P2860 | cites work | Missense mutations in β-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker-Warburg syndrome. | Q36731388 |
Deciphering the glycosylome of dystroglycanopathies using haploid screens for lassa virus entry | Q37572562 | ||
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 | Q38349218 | ||
Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies | Q42524150 | ||
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LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies. | Q47375901 | ||
Presenilin 1 regulates the processing of beta-amyloid precursor protein C-terminal fragments and the generation of amyloid beta-protein in endoplasmic reticulum and Golgi | Q48334621 | ||
Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE | Q24301093 | ||
Demonstration of mammalian protein O-mannosyltransferase activity: coexpression of POMT1 and POMT2 required for enzymatic activity | Q24303491 | ||
ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome | Q24316024 | ||
Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan | Q24321692 | ||
The protein kinase complement of the human genome | Q24324497 | ||
A novel human beta1,3-N-acetylgalactosaminyltransferase that synthesizes a unique carbohydrate structure, GalNAcbeta1-3GlcNAc | Q28511795 | ||
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O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding. | Q34090655 | ||
Like-acetylglucosaminyltransferase (LARGE)-dependent modification of dystroglycan at Thr-317/319 is required for laminin binding and arenavirus infection. | Q34223029 | ||
Glycomic analyses of mouse models of congenital muscular dystrophy | Q35065134 | ||
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Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome | Q36439344 | ||
Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephaly | Q36451494 | ||
P433 | issue | 6148 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | glycosylation | Q898365 |
carbohydrate phosphorylation | Q14863084 | ||
Beta-1,3-N-acetylgalactosaminyltransferase 2 | Q21109542 | ||
Protein O-mannose kinase | Q21121418 | ||
Protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-) | Q21123155 | ||
Protein-O-mannose kinase | Q21986759 | ||
Protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2 | Q21990911 | ||
P304 | page(s) | 896-899 | |
P577 | publication date | 2013-08-08 | |
P1433 | published in | Science | Q192864 |
P1476 | title | SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function | |
P478 | volume | 341 |
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Q46448834 | Protein O-Linked Mannose β-1,4-N-Acetylglucosaminyl-transferase 2 (POMGNT2) Is a Gatekeeper Enzyme for Functional Glycosylation of α-Dystroglycan |
Q37698536 | Protein O-mannosylation in metazoan organisms |
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Q34469573 | Secretome analysis identifies novel signal Peptide peptidase-like 3 (Sppl3) substrates and reveals a role of Sppl3 in multiple Golgi glycosylation pathways |
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Q38186249 | Solving glycosylation disorders: fundamental approaches reveal complicated pathways |
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Q32884430 | The Muscular Dystrophy Gene TMEM5 Encodes a Ribitol β1,4-Xylosyltransferase Required for the Functional Glycosylation of Dystroglycan |
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Q32884479 | The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan addition |
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Q57562533 | Third International Workshop for Glycosylation Defects in Muscular Dystrophies, 18-19 April 2013, Charlotte, USA |
Q28115432 | Xylose phosphorylation functions as a molecular switch to regulate proteoglycan biosynthesis |
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