| scholarly article | Q13442814 |
| P50 | author | Doron Betel | Q28914806 |
| P2093 | author name string | Doron BETEL | |
| Harry SCHACHTER | |||
| Wenli ZHANG | |||
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| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 153 | |
| P577 | publication date | 2002-01-01 | |
| P1433 | published in | Biochemical Journal | Q864221 |
| P1476 | title | Cloning and expression of a novel UDP-GlcNAc:α-d-mannoside β1,2-N-acetylglucosaminyltransferase homologous to UDP-GlcNAc:α-3-d-mannoside β1,2-N-acetylglucosaminyltransferase I | |
| P478 | volume | 361 |
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| Q33566548 | Comparison of the substrate specificities and catalytic properties of the sister N-acetylglucosaminyltransferases, GnT-V and GnT-Vb (IX). |
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| Q36855555 | Congenital muscular dystrophies involving the O-mannose pathway |
| Q36217346 | Developmental expression of the neuron-specific N-acetylglucosaminyltransferase Vb (GnT-Vb/IX) and identification of its in vivo glycan products in comparison with those of its paralog, GnT-V |
| Q34217566 | Differential glycosylation of α-dystroglycan and proteins other than α-dystroglycan by like-glycosyltransferase |
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| Q94570299 | Eyes shut homolog (EYS) interacts with matriglycan of O-mannosyl glycans whose deficiency results in EYS mislocalization and degeneration of photoreceptors |
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| Q38647928 | Novel copy number variation of POMGNT1 associated with muscle-eye-brain disease detected by next-generation sequencing |
| Q24602380 | Pikachurin interaction with dystroglycan is diminished by defective O-mannosyl glycosylation in congenital muscular dystrophy models and rescued by LARGE overexpression |
| Q37723603 | Protein O-mannosylation in animal development and physiology: from human disorders to Drosophila phenotypes |
| Q34980261 | Protein O-mannosylation: conserved from bacteria to humans |
| Q36981050 | Receptor tyrosine phosphatase beta (RPTPbeta) activity and signaling are attenuated by glycosylation and subsequent cell surface galectin-1 binding |
| Q34032485 | Retinal ectopias and mechanically weakened basement membrane in a mouse model of muscle-eye-brain (MEB) disease congenital muscular dystrophy |
| Q35222634 | Synthetic, structural, and biosynthetic studies of an unusual phospho-glycopeptide derived from α-dystroglycan |
| Q35824015 | The role of defective glycosylation in congenital muscular dystrophy |
| Q34989555 | The role of the GlcNAc(beta)1,2Man(alpha)- moiety in mammalian development. Null mutations of the genes encoding UDP-N-acetylglucosamine:alpha-3-D-mannoside beta-1,2-N-acetylglucosaminyltransferase I and UDP-N-acetylglucosamine:alpha-D-mannoside bet |
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