(Q34989520)

5 August 2017

1 reference

title

Mutation of Large, which encodes a putative glycosyltransferase, in an animal model of muscular dystrophy (English)

1 reference

5 August 2017

Prabhjit K Grewal

1

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5 August 2017

Jane E Hewitt

series ordinal

2

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5 August 2017

language of work or name

English

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publication date

1 December 2002

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5 August 2017

number of pages

9

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Biochimica et Biophysica Acta

inferred from page(s)

published in

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5 August 2017

volume

1573

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5 August 2017

issue

3

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5 August 2017

page(s)

216-224

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cDNA Cloning and Expression of a Family of UDP-N-acetyl-dgalactosamine:PolypeptideN-Acetylgalactosaminyltransferase Sequence Homologs fromCaenorhabditis elegans

5 August 2017

cites work

1 reference

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7 January 2021

Expression of three Caenorhabditis elegans N-acetylglucosaminyltransferase I genes during development

1 reference

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7 January 2021

Animal models for muscular dystrophy: valuable tools for the development of therapies

1 reference

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7 January 2021

Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q

1 reference

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7 January 2021

Genetic mapping near the myd locus on mouse chromosome 8

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

A syntrophin gene maps to mouse chromosome 8 and is not the myodystrophy gene

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

The Ant1 gene maps near Klk3 on proximal mouse chromosome 8

1 reference

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7 January 2021

Genetic and Physical Mapping of a Voltage-Dependent Chloride Channel Gene to Human 4q32 and to Mouse 8

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8.

1 reference

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7 January 2021

High-resolution mapping of mouse chromosome 8 identifies an evolutionary chromosomal breakpoint

1 reference

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7 January 2021

The DNA sequence of human chromosome 22

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Human chromosome 19 and related regions in mouse: conservative and lineage-specific evolution

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

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

1 reference

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7 January 2021

Molecular basis for structural diversity in the core regions of the lipopolysaccharides of Escherichia coli and Salmonella enterica

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Myodystrophy, a new myopathy on chromosome 8 of the mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Naked axons in myodystrophic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Identification of a novel mutant transcript of laminin α2 chain gene responsible for muscular dystrophy and dysmyelination in dy2J mice

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Dystroglycan in development and disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Assembly of the sarcoglycan complex. Insights for muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Biosynthesis of dystroglycan: processing of a precursor propeptide

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Membrane organization of the dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Dystroglycan binds nerve and muscle agrin

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Chimaeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapses

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Binding of the G domains of laminin alpha1 and alpha2 chains and perlecan to heparin, sulfatides, alpha-dystroglycan and several extracellular matrix proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

A role for dystroglycan in basement membrane assembly

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Dystroglycan inside and out.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Identification and purification of an agrin receptor from Torpedo postsynaptic membranes: a heteromeric complex related to the dystroglycans

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

A role for dystrophin-associated glycoproteins and utrophin in agrin-induced AChR clustering

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

The relationship between perlecan and dystroglycan and its implication in the formation of the neuromuscular junction.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

A stoichiometric complex of neurexins and dystroglycan in brain

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

The complexities of dystroglycan

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Identification of alpha-dystroglycan as a receptor for lymphocytic choriomeningitis virus and Lassa fever virus

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Role of alpha-dystroglycan as a Schwann cell receptor for Mycobacterium leprae

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Molecular basis for the peripheral nerve predilection of Mycobacterium leprae

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Murine muscular dystrophy caused by a mutation in the laminin alpha 2 (Lama2) gene

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Congenital muscular dystrophy: from rags to riches

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Non-muscle alpha-dystroglycan is involved in epithelial development

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Structure/function studies of glycosyltransferases

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

The fukutin protein family--predicted enzymes modifying cell-surface molecules

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Cloning and expression of a novel UDP-GlcNAc:α-d-mannoside β1,2-N-acetylglucosaminyltransferase homologous to UDP-GlcNAc:α-3-d-mannoside β1,2-N-acetylglucosaminyltransferase I

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Glycoprotein structure determination by mass spectrometry

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Genetic remodeling of protein glycosylation in vivo induces autoimmune disease

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

In vitro interactions of Caenorhabditis elegans dystrophin with dystrobrevin and syntrophin.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

Mutations in the dystrophin-like dys-1 gene of Caenorhabditis elegans result in reduced acetylcholinesterase activity.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900387-2

7 January 2021

10.1016/S0304-4165(02)00387-2

Identifiers

DOI

1 reference

5 August 2017

1 reference