| scholarly article | Q13442814 |
| P356 | DOI | 10.1074/JBC.M103843200 |
| P698 | PubMed publication ID | 11459841 |
| P2093 | author name string | Ervasti JM | |
| Combs AC | |||
| McDearmon EL | |||
| P2860 | cites work | Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy | Q24310537 |
| epsilon-Sarcoglycan, a broadly expressed homologue of the gene mutated in limb-girdle muscular dystrophy 2D | Q24314855 | ||
| The dystroglycan complex is necessary for stabilization of acetylcholine receptor clusters at neuromuscular junctions and formation of the synaptic basement membrane | Q24670500 | ||
| The small leucine-rich repeat proteoglycan biglycan binds to alpha-dystroglycan and is upregulated in dystrophic muscle | Q24680849 | ||
| Interactions between beta 2-syntrophin and a family of microtubule-associated serine/threonine kinases | Q28139505 | ||
| Chimaeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapses | Q28141198 | ||
| Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix | Q28296676 | ||
| Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle | Q28510608 | ||
| Alternative splicing of agrin regulates its binding to heparin alpha-dystroglycan, and the cell surface | Q28574863 | ||
| Differential Association of Syntrophin Pairs with the Dystrophin Complex | Q28584710 | ||
| Distinct phenotypes of mutant mice lacking agrin, MuSK, or rapsyn | Q28584895 | ||
| Membrane organization of the dystrophin-glycoprotein complex | Q29615149 | ||
| Dystroglycan inside and out. | Q33744965 | ||
| Muscular dystrophies and the dystrophin-glycoprotein complex | Q34425741 | ||
| A postsynaptic Mr 58,000 (58K) protein concentrated at acetylcholine receptor-rich sites in Torpedo electroplaques and skeletal muscle | Q36216287 | ||
| A novel 87,000-Mr protein associated with acetylcholine receptors in Torpedo electric organ and vertebrate skeletal muscle | Q36221592 | ||
| A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin. | Q36232550 | ||
| A functional role for specific spliced variants of the alpha7beta1 integrin in acetylcholine receptor clustering | Q36255897 | ||
| Laminin-induced acetylcholine receptor clustering: an alternative pathway | Q36273941 | ||
| Differential membrane localization and intermolecular associations of alpha-dystrobrevin isoforms in skeletal muscle | Q36290588 | ||
| Localization of the DMDL gene-encoded dystrophin-related protein using a panel of nineteen monoclonal antibodies: presence at neuromuscular junctions, in the sarcolemma of dystrophic skeletal muscle, in vascular and other smooth muscles, and in prol | Q36530515 | ||
| Acetylcholine receptor distribution on myotubes in culture correlated to acetylcholine sensitivity | Q36835480 | ||
| Differentiation markers of mouse C2C12 and rat L6 myogenic cell lines and the effect of the differentiation medium | Q40930406 | ||
| Role for a synapse-specific carbohydrate in agrin-induced clustering of acetylcholine receptors | Q41354044 | ||
| Maturation and maintenance of the neuromuscular synapse: genetic evidence for roles of the dystrophin--glycoprotein complex | Q42485105 | ||
| Characterization of dp6troglycan-laminin interaction in peripheral nerve. | Q42517423 | ||
| Dystrophin-glycoprotein complex is highly enriched in isolated skeletal muscle sarcolemma | Q43107646 | ||
| Tissue-specific heterogeneity in alpha-dystroglycan sialoglycosylation. Skeletal muscle alpha-dystroglycan is a latent receptor for Vicia villosa agglutinin b4 masked by sialic acid modification | Q48634703 | ||
| Immunolocalization and developmental expression of dystrophin related protein in skeletal muscle. | Q52238869 | ||
| Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle | Q59089242 | ||
| epsilon-sarcoglycan replaces alpha-sarcoglycan in smooth muscle to form a unique dystrophin-glycoprotein complex | Q64381267 | ||
| Dystrophin-related protein is localized to neuromuscular junctions of adult skeletal muscle | Q68255626 | ||
| Neural regulation of alpha-dystroglycan biosynthesis and glycosylation in skeletal muscle | Q73315875 | ||
| A mechanism for acetylcholine receptor clustering distinct from agrin signaling | Q73368357 | ||
| Skeletal and cardiac myopathies in mice lacking utrophin and dystrophin: a model for Duchenne muscular dystrophy | Q73677664 | ||
| The formation of neuromuscular synapses | Q74070428 | ||
| Agrin-independent activation of the agrin signal transduction pathway | Q78107668 | ||
| Biochemical characterization of the epithelial dystroglycan complex | Q78208215 | ||
| P433 | issue | 37 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Vicia villosa | Q159752 |
| P304 | page(s) | 35078-35086 | |
| P577 | publication date | 2001-07-17 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Differential Vicia villosa agglutinin reactivity identifies three distinct dystroglycan complexes in skeletal muscle | |
| P478 | volume | 276 |
| Q24321993 | A comparative study of alpha-dystroglycan glycosylation in dystroglycanopathies suggests that the hypoglycosylation of alpha-dystroglycan does not consistently correlate with clinical severity |
| Q28589413 | Brain alpha-dystroglycan displays unique glycoepitopes and preferential binding to laminin-10/11 |
| Q43052323 | Characterization of site-specific O-glycan structures within the mucin-like domain of alpha-dystroglycan from human skeletal muscle |
| Q38350844 | Core 1 glycans on alpha-dystroglycan mediate laminin-induced acetylcholine receptor clustering but not laminin binding |
| Q48259349 | Defective peripheral nerve myelination and neuromuscular junction formation in fukutin-deficient chimeric mice |
| Q41642554 | Differentiation-related glycan epitopes identify discrete domains of the muscle glycocalyx |
| Q24791187 | Diversity of the Brain Dystrophin-Glycoprotein Complex. |
| Q38326990 | Enhanced laminin binding by alpha-dystroglycan after enzymatic deglycosylation |
| Q48114812 | Formation of multiple complexes between beta-dystroglycan and dystrophin family products |
| Q36581125 | ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies |
| Q30476990 | Induction of myasthenia by immunization against muscle-specific kinase |
| Q28206352 | Induction, assembly, maturation and maintenance of a postsynaptic apparatus |
| Q37329563 | Muscular dystrophies due to glycosylation defects |
| Q34983110 | Mutational and functional analysis of Large in a novel CHO glycosylation mutant |
| Q46703440 | Versican in the developing brain: lamina-specific expression in interneuronal subsets and role in presynaptic maturation. |
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