Mutant glycosyltransferase and altered glycosylation of alpha-dystroglycan in the myodystrophy mouse (Q28589172)

31 January 2017

title

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

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LARGE xylosyl- and glucuronyltransferase 1

31 January 2017

main subject

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GOA release 2020-03-11

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P. K. Grewal

1

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31 January 2017

P. J. Holzfeind

series ordinal

2

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31 January 2017

R. E. Bittner

series ordinal

3

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31 January 2017

J. E. Hewitt

series ordinal

4

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31 January 2017

language of work or name

English

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publication date

1 June 2001

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31 January 2017

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31 January 2017

volume

28

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31 January 2017

issue

2

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31 January 2017

page(s)

151–154

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Direct interaction of Smn with dp103, a putative RNA helicase: a role for Smn in transcription regulation?

31 January 2017

cites work

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7 January 2021

Myodystrophy, a new myopathy on chromosome 8 of the mouse

1 reference

7 January 2021

Phenotypic and pathologic evaluation of the myd mouse. A candidate model for facioscapulohumeral dystrophy.

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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

7 January 2021

Genetic mapping near the myd locus on mouse chromosome 8

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7 January 2021

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

1 reference

7 January 2021

FRG1, a gene in the FSH muscular dystrophy region on human chromosome 4q35, is highly conserved in vertebrates and invertebrates

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7 January 2021

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

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7 January 2021

Cloning of the murine unconventional myosin gene Myo9b and identification of alternative splicing

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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

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7 January 2021

Structure/function studies of glycosyltransferases

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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

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7 January 2021

Dystroglycan in development and disease.

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7 January 2021

Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophy

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7 January 2021

Membrane organization of the dystrophin-glycoprotein complex

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

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7 January 2021

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

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7 January 2021

CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

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7 January 2021

Dystroglycan is a binding protein of laminin and merosin in peripheral nerve

1 reference

7 January 2021