Pages that link to "Q28254849"

The following pages link to Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor (Q28254849):

Displaying 50 items.

• Gamma1- and gamma2-syntrophins, two novel dystrophin-binding proteins localized in neuronal cells (Q22253448) ‎ (← links)
• Caveolin-3 directly interacts with the C-terminal tail of beta -dystroglycan. Identification of a central WW-like domain within caveolin family members (Q24290252) ‎ (← links)
• Tight junctions of the blood-brain barrier: development, composition and regulation (Q24292730) ‎ (← links)
• Nitric oxide synthase complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy (Q24307833) ‎ (← links)
• β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12 (Q24312878) ‎ (← links)
• Characterization of an Importin alpha/beta-recognized nuclear localization signal in beta-dystroglycan (Q24316092) ‎ (← links)
• Agrin is a high-affinity binding protein of dystroglycan in non-muscle tissue (Q24317041) ‎ (← links)
• Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy (Q24317764) ‎ (← links)
• Agrin binds to the nerve-muscle basal lamina via laminin (Q24321436) ‎ (← links)
• Human adhalin is alternatively spliced and the gene is located on chromosome 17q21 (Q24324815) ‎ (← links)
• Increasing complexity of the dystrophin-associated protein complex (Q24564140) ‎ (← links)
• Pikachurin interaction with dystroglycan is diminished by defective O-mannosyl glycosylation in congenital muscular dystrophy models and rescued by LARGE overexpression (Q24602380) ‎ (← links)
• Mouse fukutin deletion impairs dystroglycan processing and recapitulates muscular dystrophy (Q24611333) ‎ (← links)
• Visual impairment in the absence of dystroglycan (Q24622370) ‎ (← links)
• Biglycan binds to alpha- and gamma-sarcoglycan and regulates their expression during development (Q24623422) ‎ (← links)
• Post-translational Maturation of Dystroglycan Is Necessary for Pikachurin Binding and Ribbon Synaptic Localization (Q24634095) ‎ (← links)
• The dystroglycan complex is necessary for stabilization of acetylcholine receptor clusters at neuromuscular junctions and formation of the synaptic basement membrane (Q24670500) ‎ (← links)
• The small leucine-rich repeat proteoglycan biglycan binds to alpha-dystroglycan and is upregulated in dystrophic muscle (Q24680849) ‎ (← links)
• Mechanistic distinctions between agrin and laminin-1 induced aggregation of acetylcholine receptors (Q24803293) ‎ (← links)
• A stoichiometric complex of neurexins and dystroglycan in brain (Q26269938) ‎ (← links)
• The biochemical and mass spectrometric profiling of the dystrophin complexome from skeletal muscle (Q26770343) ‎ (← links)
• Mammalian O-mannosylation: unsolved questions of structure/function (Q26860991) ‎ (← links)
• O-Mannosylation and human disease (Q27014986) ‎ (← links)
• The crystal structure of a laminin G-like module reveals the molecular basis of alpha-dystroglycan binding to laminins, perlecan, and agrin (Q27620848) ‎ (← links)
• Interactions between beta 2-syntrophin and a family of microtubule-associated serine/threonine kinases (Q28139505) ‎ (← links)
• Chimaeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapses (Q28141198) ‎ (← links)
• Adhesion of cultured bovine aortic endothelial cells to laminin-1 mediated by dystroglycan (Q28141804) ‎ (← links)
• Induction, assembly, maturation and maintenance of a postsynaptic apparatus (Q28206352) ‎ (← links)
• A role of dystroglycan in schwannoma cell adhesion to laminin (Q28238357) ‎ (← links)
• Dystroglycan is a binding protein of laminin and merosin in peripheral nerve (Q28238540) ‎ (← links)
• Gephyrin clusters are absent from small diameter primary afferent terminals despite the presence of GABA(A) receptors (Q28241834) ‎ (← links)
• Characterization of the LARGE family of putative glycosyltransferases associated with dystroglycanopathies (Q28256756) ‎ (← links)
• Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins (Q28257712) ‎ (← links)
• Agrin receptors at the skeletal neuromuscular junction (Q28276814) ‎ (← links)
• Characterization of Gas6, a member of the superfamily of G domain-containing proteins, as a ligand for Rse and Axl (Q28277798) ‎ (← links)
• The receptor tyrosine kinase MuSK is required for neuromuscular junction formation in vivo (Q28280767) ‎ (← links)
• Agrin acts via a MuSK receptor complex (Q28280777) ‎ (← links)
• The complete cDNA sequence of laminin alpha 4 and its relationship to the other human laminin alpha chains (Q28284795) ‎ (← links)
• Agrin is a heparan sulfate proteoglycan (Q28307146) ‎ (← links)
• Expression of agrin, dystroglycan, and utrophin in normal renal tissue and in experimental glomerulopathies (Q28344242) ‎ (← links)
• A high throughput screen identifies chemical modulators of the laminin-induced clustering of dystroglycan and aquaporin-4 in primary astrocytes (Q28477344) ‎ (← links)
• Lrp4 is a receptor for Agrin and forms a complex with MuSK (Q28505665) ‎ (← links)
• Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation (Q28507319) ‎ (← links)
• LRP4 serves as a coreceptor of agrin (Q28508023) ‎ (← links)
• Agrin (Q28560915) ‎ (← links)
• The COOH-terminal domain of agrin signals via a synaptic receptor in central nervous system neurons (Q28564406) ‎ (← links)
• Laminin-alpha2 chain-like antigens in CNS dendritic spines (Q28565855) ‎ (← links)
• A set of genes expressed in response to light in the adult cerebral cortex and regulated during development (Q28566011) ‎ (← links)
• Increased expression of dystrophin, beta-dystroglycan and adhalin in denervated rat muscles (Q28567784) ‎ (← links)
• Evidence that dystroglycan is associated with dynamin and regulates endocytosis (Q28569266) ‎ (← links)