| scholarly article | Q13442814 |
| P2093 | author name string | Erhard Hohenester | |
| P2860 | cites work | 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 | ||
| B4GAT1 is the priming enzyme for the LARGE-dependent functional glycosylation of α-dystroglycan | Q24305043 | ||
| The glucuronyltransferase B4GAT1 is required for initiation of LARGE-mediated α-dystroglycan functional glycosylation | Q24305058 | ||
| Identification of a 2 Mb human ortholog of Drosophila eyes shut/spacemaker that is mutated in patients with retinitis pigmentosa | Q24310728 | ||
| SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function | Q24316126 | ||
| EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa | Q24319794 | ||
| Structure of the C-terminal laminin G-like domain pair of the laminin alpha2 chain harbouring binding sites for alpha-dystroglycan and heparin | Q24630865 | ||
| Post-translational Maturation of Dystroglycan Is Necessary for Pikachurin Binding and Ribbon Synaptic Localization | Q24634095 | ||
| A stoichiometric complex of neurexins and dystroglycan in brain | Q26269938 | ||
| Crystal structure of the second LNS/LG domain from neurexin 1alpha: Ca2+ binding and the effects of alternative splicing | Q26269940 | ||
| The crystal structure of a laminin G-like module reveals the molecular basis of alpha-dystroglycan binding to laminins, perlecan, and agrin | Q27620848 | ||
| Distinct requirements for heparin and alpha-dystroglycan binding revealed by structure-based mutagenesis of the laminin alpha2 LG4-LG5 domain pair | Q27641994 | ||
| Structure of a C-type mannose-binding protein complexed with an oligosaccharide | Q27642164 | ||
| Crystal Structure and Cell Surface Anchorage Sites of Laminin 1LG4-5 | Q27643849 | ||
| Human ISPD Is a Cytidyltransferase Required for Dystroglycan O-Mannosylation | Q27703190 | ||
| Xylose phosphorylation functions as a molecular switch to regulate proteoglycan biosynthesis | Q28115432 | ||
| Modulation of agrin function by alternative splicing and Ca2+ binding | Q28249942 | ||
| Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation | Q28507319 | ||
| LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy | Q28512184 | ||
| Dystroglycan organizes axon guidance cue localization and axonal pathfinding | Q28593913 | ||
| Laminins during muscle development and in muscular dystrophies | Q30654764 | ||
| Structural basis of laminin binding to the LARGE glycans on dystroglycan | Q31121747 | ||
| The Muscular Dystrophy Gene TMEM5 Encodes a Ribitol β1,4-Xylosyltransferase Required for the Functional Glycosylation of Dystroglycan | Q32884430 | ||
| The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan addition | Q32884479 | ||
| Site mapping and characterization of O-glycan structures on alpha-dystroglycan isolated from rabbit skeletal muscle. | Q34042753 | ||
| O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding. | Q34090655 | ||
| Glycoproteomic characterization of recombinant mouse α-dystroglycan | Q34126184 | ||
| Like-acetylglucosaminyltransferase (LARGE)-dependent modification of dystroglycan at Thr-317/319 is required for laminin binding and arenavirus infection. | Q34223029 | ||
| Differential heparin inhibition of skeletal muscle alpha-dystroglycan binding to laminins | Q34379897 | ||
| Heparin modulation of laminin polymerization | Q34433284 | ||
| Glycomic analyses of mouse models of congenital muscular dystrophy | Q35065134 | ||
| A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin. | Q36232550 | ||
| Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome | Q36439344 | ||
| Laminins in basement membrane assembly | Q36531811 | ||
| ISPD produces CDP-ribitol used by FKTN and FKRP to transfer ribitol phosphate onto α-dystroglycan | Q36919737 | ||
| Carbohydrate-binding domain of the POMGnT1 stem region modulates O-mannosylation sites of α-dystroglycan | Q37200133 | ||
| Mining the O-mannose glycoproteome reveals cadherins as major O-mannosylated glycoproteins | Q37421355 | ||
| LARGE2-dependent glycosylation confers laminin-binding ability on proteoglycans. | Q37472546 | ||
| Eyes shut homolog is required for maintaining the ciliary pocket and survival of photoreceptors in zebrafish | Q37502243 | ||
| Deciphering the glycosylome of dystroglycanopathies using haploid screens for lassa virus entry | Q37572562 | ||
| Ablation of EYS in zebrafish causes mislocalisation of outer segment proteins, F-actin disruption and cone-rod dystrophy | Q37737834 | ||
| Heparan sulfate biosynthesis: regulation and variability | Q38050077 | ||
| Biosynthesis and function of chondroitin sulfate | Q38115113 | ||
| Molecular dissection of the alpha-dystroglycan- and integrin-binding sites within the globular domain of human laminin-10. | Q38346410 | ||
| Matriglycan: a novel polysaccharide that links dystroglycan to the basement membrane. | Q38424785 | ||
| Recent insights into structures and functions of C-type lectins in the immune system | Q38545140 | ||
| Crystal Structure of the Heterotrimeric Integrin-Binding Region of Laminin-111. | Q38718919 | ||
| Glycosylation with ribitol-phosphate in mammals: New insights into the O-mannosyl glycan | Q39437022 | ||
| Recent advancements in understanding mammalian O-mannosylation | Q40092479 | ||
| Building synapses: agrin and dystroglycan stick together | Q40397631 | ||
| Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage. | Q40612428 | ||
| Mechanistic basis for the recognition of laminin-511 by α6β1 integrin. | Q41591759 | ||
| Dystroglycan binding to α-neurexin competes with neurexophilin-1 and neuroligin in the brain. | Q41987606 | ||
| Binding of the G domains of laminin alpha1 and alpha2 chains and perlecan to heparin, sulfatides, alpha-dystroglycan and several extracellular matrix proteins | Q42001102 | ||
| Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies | Q42524150 | ||
| Direct Mapping of Additional Modifications on Phosphorylated O-glycans of α-Dystroglycan by Mass Spectrometry Analysis in Conjunction with Knocking Out of Causative Genes for Dystroglycanopathy | Q42687793 | ||
| Protein O-Linked Mannose β-1,4-N-Acetylglucosaminyl-transferase 2 (POMGNT2) Is a Gatekeeper Enzyme for Functional Glycosylation of α-Dystroglycan | Q46448834 | ||
| Muscular Dystrophy with Ribitol-Phosphate Deficiency: A Novel Post-Translational Mechanism in Dystroglycanopathy | Q47168266 | ||
| EYS mutation update: In silico assessment of 271 reported and 26 novel variants in patients with retinitis pigmentosa. | Q47380003 | ||
| Laminin-binding protein 120 from brain is closely related to the dystrophin-associated glycoprotein, dystroglycan, and binds with high affinity to the major heparin binding domain of laminin | Q48249023 | ||
| Identification of a Post-translational Modification with Ribitol-Phosphate and Its Defect in Muscular Dystrophy | Q48873234 | ||
| Activation of muscle-specific receptor tyrosine kinase and binding to dystroglycan are regulated by alternative mRNA splicing of agrin | Q79165764 | ||
| O-Mannose and O-N-acetyl galactosamine glycosylation of mammalian α-dystroglycan is conserved in a region-specific manner | Q84558838 | ||
| Muscular dystrophies | Q86291937 | ||
| CDP-glycerol inhibits the synthesis of the functional O-mannosyl glycan of α-dystroglycan | Q89047205 | ||
| P304 | page(s) | 56-63 | |
| P577 | publication date | 2018-12-06 | |
| P1433 | published in | Current Opinion in Structural Biology | Q15758416 |
| P1476 | title | Laminin G-like domains: dystroglycan-specific lectins | |
| P478 | volume | 56 |
| Q90245857 | An improved method for culturing myotubes on laminins for the robust clustering of postsynaptic machinery |
| Q90154126 | HNK-1 Sulfotransferase modulates α-dystroglycan glycosylation by 3-O-sulfation of glucuronic acid on matriglycan |
| Q92535136 | Linker Protein Repair of LAMA2 Dystrophic Neuromuscular Basement Membranes |
| Q99716328 | POMK regulates dystroglycan function via LARGE-mediated elongation of matriglycan |
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