scholarly article | Q13442814 |
P50 | author | Geert-Jan Boons | Q38318328 |
Kelley W Moremen | Q56917016 | ||
P2093 | author name string | Shuo Wang | |
Lance Wells | |||
Zoeisha S Chinoy | |||
David H Live | |||
Annapoorani Ramiah | |||
Jeremy L Praissman | |||
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Missense mutations in β-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker-Warburg syndrome. | Q36731388 | ||
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Loss of alpha-dystroglycan laminin binding in epithelium-derived cancers is caused by silencing of LARGE. | Q37160880 | ||
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Protein O-mannosylation is crucial for E-cadherin-mediated cell adhesion | Q37421256 | ||
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Suppression of B3GNT7 gene expression in colon adenocarcinoma and its potential effect in the metastasis of colon cancer cells | Q39034783 | ||
B3GNT3 expression suppresses cell migration and invasion and predicts favorable outcomes in neuroblastoma | Q39080654 | ||
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O-glycosylation of the non-canonical T-cadherin from rabbit skeletal muscle by single mannose residues | Q43528757 | ||
160 kb deletion in ISPD unmasking a recessive mutation in a patient with Walker-Warburg syndrome | Q46105701 | ||
A truncating mutation in B3GNT1 causes severe Walker-Warburg syndrome | Q47956367 | ||
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Impaired sexual behavior in male mice deficient for the beta1-3 N-acetylglucosaminyltransferase-I gene. | Q51727809 | ||
??? | Q22009535 | ||
P407 | language of work or name | English | Q1860 |
P921 | main subject | poly-N-acetyllactosamine biosynthetic process | Q21108245 |
Beta-1,4-glucuronyltransferase 1 | Q21108246 | ||
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 | Q21109547 | ||
LARGE xylosyl- and glucuronyltransferase 1 | Q21117620 | ||
glycosylation | Q898365 | ||
P577 | publication date | 2014-01-01 | |
P1433 | published in | eLife | Q2000008 |
P1476 | title | B4GAT1 is the priming enzyme for the LARGE-dependent functional glycosylation of α-dystroglycan | |
P478 | volume | 3 |
Q42506388 | 3D structural analysis of protein O-mannosyl kinase, POMK, a causative gene product of dystroglycanopathy. |
Q90362813 | A new patient-derived iPSC model for dystroglycanopathies validates a compound that increases glycosylation of α-dystroglycan |
Q57458034 | A two-phase model for the non-processive biosynthesis of homogalacturonan polysaccharides by the GAUT1:GAUT7 complex |
Q89047205 | CDP-glycerol inhibits the synthesis of the functional O-mannosyl glycan of α-dystroglycan |
Q37709546 | Clear differences in cerebrospinal fluid proteome between women with chronic widespread pain and healthy women - a multivariate explorative cross-sectional study |
Q92711724 | Crystal structures of fukutin-related protein (FKRP), a ribitol-phosphate transferase related to muscular dystrophy |
Q41642554 | Differentiation-related glycan epitopes identify discrete domains of the muscle glycocalyx |
Q35709549 | Ectopic clustering of Cajal-Retzius and subplate cells is an initial pathological feature in Pomgnt2-knockout mice, a model of dystroglycanopathy. |
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Q36919737 | ISPD produces CDP-ribitol used by FKTN and FKRP to transfer ribitol phosphate onto α-dystroglycan |
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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 |
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Q32884430 | The Muscular Dystrophy Gene TMEM5 Encodes a Ribitol β1,4-Xylosyltransferase Required for the Functional Glycosylation of Dystroglycan |
Q28546951 | The Structure of the T190M Mutant of Murine α-Dystroglycan at High Resolution: Insight into the Molecular Basis of a Primary Dystroglycanopathy |
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Q32884479 | The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan addition |
Q28085305 | The secretory pathway kinases |
Q38796983 | What Have We Learned from Glycosyltransferase Knockouts in Mice? |
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