Mouse large can modify complex N- and mucin O-glycans on alpha-dystroglycan to induce laminin binding (Q34405965)

2 August 2017

Mouse large can modify complex N- and mucin O-glycans on alpha-dystroglycan to induce laminin binding (English)

1 reference

2 August 2017

Santosh K Patnaik

1

1 reference

PubMed ID

15788414

2 August 2017

Pamela Stanley

series ordinal

2

1 reference

PubMed ID

15788414

2 August 2017

language of work or name

English

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publication date

23 March 2005

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Journal of Biological Chemistry

2 August 2017

9

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based on heuristic

inferred from page(s)

published in

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2 August 2017

280

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2 August 2017

20851-20859

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2 August 2017

21

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The human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene family

2 August 2017

1 reference

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Mutant glycosyltransferase and altered glycosylation of alpha-dystroglycan in the myodystrophy mouse

21 January 2018

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Skeletal, cardiac and tongue muscle pathology, defective retinal transmission, and neuronal migration defects in the Large(myd) mouse defines a natural model for glycosylation-deficient muscle - eye - brain disorders

21 January 2018

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Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1

21 January 2018

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Loss-of-function of an N-acetylglucosaminyltransferase, POMGnT1, in muscle-eye-brain disease

21 January 2018

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Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

21 January 2018

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Cranin: a laminin-binding protein of cell membranes

21 January 2018

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Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor

21 January 2018

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A stoichiometric complex of neurexins and dystroglycan in brain

21 January 2018

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Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization

21 January 2018

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Influence of core protein sequence on glycosaminoglycan assembly

21 January 2018

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A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin.

21 January 2018

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Purification of cranin, a laminin binding membrane protein. Identity with dystroglycan and reassessment of its carbohydrate moieties

21 January 2018

1 reference

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LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies.

21 January 2018

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Membrane organization of the dystrophin-glycoprotein complex

21 January 2018

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Core 1 glycans on alpha-dystroglycan mediate laminin-induced acetylcholine receptor clustering but not laminin binding

21 January 2018

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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.

21 January 2018

1 reference

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Molecular recognition by LARGE is essential for expression of functional dystroglycan

21 January 2018

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The role of defective glycosylation in congenital muscular dystrophy

21 January 2018

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Defective glycosylation in congenital muscular dystrophies

21 January 2018

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Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies

21 January 2018

1 reference

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Demonstration of mammalian protein O-mannosyltransferase activity: coexpression of POMT1 and POMT2 required for enzymatic activity

21 January 2018

1 reference

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Mutations of the POMT1 gene found in patients with Walker-Warburg syndrome lead to a defect of protein O-mannosylation

21 January 2018

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Phenotypic spectrum associated with mutations in the fukutin-related protein gene.

21 January 2018

1 reference

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New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families

21 January 2018

1 reference

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An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

21 January 2018

1 reference

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A homozygous nonsense mutation in the fukutin gene causes a Walker-Warburg syndrome phenotype

21 January 2018

1 reference

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Mutations in the FKRP gene can cause muscle-eye-brain disease and Walker-Warburg syndrome.

21 January 2018

1 reference

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Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan

21 January 2018

1 reference

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Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy

21 January 2018

1 reference

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Chinese hamster ovary cells selected for resistance to the cytotoxicity of phytohemagglutinin are deficient in a UDP-N-acetylglucosamine--glycoprotein N-acetylglucosaminyltransferase activity

21 January 2018

1 reference

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Chinese hamster ovary cell mutants with multiple glycosylation defects for production of glycoproteins with minimal carbohydrate heterogeneity

21 January 2018

1 reference

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Two Chinese hamster ovary glycosylation mutants affected in the conversion of GDP-mannose to GDP-fucose

21 January 2018

1 reference

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Mutant of Chinese hamster ovary cells with altered mannose 6-phosphate receptor activity is unable to synthesize mannosylphosphoryldolichol

21 January 2018

1 reference

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HUNT: launch of a full-length cDNA database from the Helix Research Institute

21 January 2018

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The Lec4A CHO glycosylation mutant arises from miscompartmentalization of a Golgi glycosyltransferase

21 January 2018

1 reference

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Molecular analysis of the interaction of LCMV with its cellular receptor [alpha]-dystroglycan.

21 January 2018

1 reference

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Prediction, conservation analysis, and structural characterization of mammalian mucin-type O-glycosylation sites

21 January 2018

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ELM server: A new resource for investigating short functional sites in modular eukaryotic proteins

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Cloning and characterization of mammalian UDP-glucose glycoprotein: glucosyltransferase and the development of a specific substrate for this enzyme

21 January 2018

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Two homologues encoding human UDP-glucose:glycoprotein glucosyltransferase differ in mRNA expression and enzymatic activity

21 January 2018

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Expression cloning of cDNA encoding a human beta-1,3-N-acetylglucosaminyltransferase that is essential for poly-N-acetyllactosamine synthesis

21 January 2018

1 reference

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Temporal and spatial appearance of alpha-dystroglycan in differentiated mouse myoblasts in culture

21 January 2018

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Five Lec1 CHO cell mutants have distinct Mgat1 gene mutations that encode truncated N-acetylglucosaminyltransferase I.

21 January 2018

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Differential involvement of cell surface sialic acid residues in wheat germ agglutinin binding to parental and wheat germ agglutinin-resistant Chinese hamster ovary cells

21 January 2018

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Mutants of the CMP-sialic acid transporter causing the Lec2 phenotype.

21 January 2018

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Point mutations identified in Lec8 Chinese hamster ovary glycosylation mutants that inactivate both the UDP-galactose and CMP-sialic acid transporters

21 January 2018

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alpha(1,3)fucosyltransferases expressed by the gain-of-function Chinese hamster ovary glycosylation mutants LEC12, LEC29, and LEC30.

21 January 2018

1 reference

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Molecular cloning and expression of GDP-D-mannose-4,6-dehydratase, a key enzyme for fucose metabolism defective in Lec13 cells

21 January 2018

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Molecular cloning of human GDP-mannose 4,6-dehydratase and reconstitution of GDP-fucose biosynthesis in vitro

21 January 2018

1 reference

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Structural analysis of sequences O-linked to mannose reveals a novel Lewis X structure in cranin (dystroglycan) purified from sheep brain.

21 January 2018

1 reference

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Molecular characterization of eukaryotic polysialyltransferase-1

21 January 2018

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Lec3 Chinese Hamster Ovary Mutants Lack UDP-N-acetylglucosamine 2-Epimerase Activity Because of Mutations in the Epimerase Domain of the Gne Gene

21 January 2018

1 reference

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A single point mutation resulting in an adversely reduced expression of DPM2 in the Lec15.1 cells

21 January 2018

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Protein C-mannosylation is enzyme-catalysed and uses dolichyl-phosphate-mannose as a precursor

21 January 2018

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Molecular cloning and expression of a novel beta-1, 6-N-acetylglucosaminyltransferase that forms core 2, core 4, and I branches

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Dystrophin and the membrane skeleton

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Specific disruption of a schwann cell dystrophin-related protein complex in a demyelinating neuropathy

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The dystrophin-glycoprotein complex, cellular signaling, and the regulation of cell survival in the muscular dystrophies

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Dystroglycan complex in cancer

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CDD: a database of conserved domain alignments with links to domain three-dimensional structure

21 January 2018

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Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve alpha-dystroglycan. The role of a novel O-mannosyl-type oligosaccharide in the binding of alpha-dystroglycan with laminin

21 January 2018

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Detection of O-mannosyl glycans in rabbit skeletal muscle alpha-dystroglycan

21 January 2018

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A Japanese patient with distal myopathy with rimmed vacuoles: missense mutations in the epimerase domain of the UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) gene accompanied by hyposialylation of skeletal muscle glycoproteins

21 January 2018

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High prevalence of 2-mono- and 2,6-di-substituted manol-terminating sequences among O-glycans released from brain glycopeptides by reductive alkaline hydrolysis.

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Molecular cloning and characterization of human GnT-IX, a novel beta1,6-N-acetylglucosaminyltransferase that is specifically expressed in the brain.

21 January 2018

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N-Acetylglucosaminyltransferase IX acts on the GlcNAc beta 1,2-Man alpha 1-Ser/Thr moiety, forming a 2,6-branched structure in brain O-mannosyl glycan.

21 January 2018

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Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia

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Deletions on chromosome 22 in sporadic meningioma

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Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle

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Identifiers

DOI

10.1074/JBC.M500069200

1 reference

2 August 2017

1 reference

PubMed ID

15788414