Enhanced laminin binding by alpha-dystroglycan after enzymatic deglycosylation.
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Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGEO-Mannosylation and human diseaseCrystal Structure and Cell Surface Anchorage Sites of Laminin 1LG4-5Identification of new dystroglycan complexes in skeletal muscleBrain alpha-dystroglycan displays unique glycoepitopes and preferential binding to laminin-10/11Structural basis of laminin binding to the LARGE glycans on dystroglycan.Identification of alpha-dystroglycan binding sequences in the laminin alpha2 chain LG4-5 moduleThe dystroglycanopathies: the new disorders of O-linked glycosylationAdeno-associated virus-mediated overexpression of LARGE rescues α-dystroglycan function in dystrophic mice with mutations in the fukutin-related protein.Site mapping and characterization of O-glycan structures on alpha-dystroglycan isolated from rabbit skeletal muscle.O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding.Glycoproteomic characterization of recombinant mouse α-dystroglycan.Like-acetylglucosaminyltransferase (LARGE)-dependent modification of dystroglycan at Thr-317/319 is required for laminin binding and arenavirus infection.miRNA-based buffering of the cobblestone-lissencephaly-associated extracellular matrix receptor dystroglycan via its alternative 3'-UTR.Phosphorylation within the cysteine-rich region of dystrophin enhances its association with β-dystroglycan and identifies a potential novel therapeutic target for skeletal muscle wasting.Mutational and functional analysis of Large in a novel CHO glycosylation mutant.Glycomic analyses of mouse models of congenital muscular dystrophyIncreased sialylation as a phenomenon in accommodation of the parasitic nematode Trichinella spiralis (Owen, 1835) in skeletal muscle fibres.Absence of post-phosphoryl modification in dystroglycanopathy mouse models and wild-type tissues expressing non-laminin binding form of α-dystroglycan.Old World and clade C New World arenaviruses mimic the molecular mechanism of receptor recognition used by alpha-dystroglycan's host-derived ligands.Dystroglycan Depletion Impairs Actin-Dependent Functions of Differentiated Kasumi-1 CellsMechanisms of disease: congenital muscular dystrophies-glycosylation takes center stage.The o-mannosylation pathway: glycosyltransferases and proteins implicated in congenital muscular dystrophy.ISPD produces CDP-ribitol used by FKTN and FKRP to transfer ribitol phosphate onto α-dystroglycan.Muscular dystrophies due to glycosylation defects.Deciphering the glycosylome of dystroglycanopathies using haploid screens for lassa virus entry.Integrin and dystroglycan compensate each other to mediate laminin-dependent basement membrane assembly and epiblast polarization.Vertebrate protein glycosylation: diversity, synthesis and function.Protein O-mannosylation in animal development and physiology: from human disorders to Drosophila phenotypesBiological role of dystroglycan in Schwann cell function and its implications in peripheral nervous system diseases.Lissencephaly with brainstem and cerebellar hypoplasia and congenital cataracts.Mammalian O-mannosylation pathway: glycan structures, enzymes, and protein substrates.Finding the sweet spot: assembly and glycosylation of the dystrophin-associated glycoprotein complex.Matriglycan: a novel polysaccharide that links dystroglycan to the basement membrane.Disease mutations in CMP-sialic acid transporter SLC35A1 result in abnormal α-dystroglycan O-mannosylation, independent from sialic acid.Initiation of mammalian O-mannosylation in vivo is independent of a consensus sequence and controlled by peptide regions within and upstream of the alpha-dystroglycan mucin domain.Dystroglycan and protein O-mannosyltransferases 1 and 2 are required to maintain integrity of Drosophila larval muscles.Alterations of dystrophin-associated glycoproteins in the heart lacking dystrophin or dystrophin and utrophin.LARGE enzyme activity deciphered: a new therapeutic target for muscular dystrophies.Characterization of site-specific O-glycan structures within the mucin-like domain of alpha-dystroglycan from human skeletal muscle.
P2860
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P2860
Enhanced laminin binding by alpha-dystroglycan after enzymatic deglycosylation.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh
2005年學術文章
@zh-hant
name
Enhanced laminin binding by alpha-dystroglycan after enzymatic deglycosylation.
@en
type
label
Enhanced laminin binding by alpha-dystroglycan after enzymatic deglycosylation.
@en
prefLabel
Enhanced laminin binding by alpha-dystroglycan after enzymatic deglycosylation.
@en
P2860
P356
P1433
P1476
Enhanced laminin binding by alpha-dystroglycan after enzymatic deglycosylation.
@en
P2093
Ariana C Combs
James M Ervasti
P2860
P304
P356
10.1042/BJ20050375
P407
P577
2005-08-01T00:00:00Z