Dystroglycan mRNA expression during normal and mdx mouse embryogenesis: a comparison with utrophin and the apo-dystrophins. (Q52205517)

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15 October 2019

title

Dystroglycan mRNA expression during normal and mdx mouse embryogenesis: a comparison with utrophin and the apo-dystrophins (English)

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15 October 2019

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2

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15 October 2019

author name string

Schofield JN

1

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15 October 2019

Blake DJ

3

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15 October 2019

Davies K

4

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15 October 2019

Edwards YH

5

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15 October 2019

publication date

1 October 1995

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15 October 2019

published in

Developmental Dynamics

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15 October 2019

volume

204

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15 October 2019

issue

2

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15 October 2019

page(s)

178-185

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The structural and functional diversity of dystrophin

15 October 2019

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A novel product of the Duchenne muscular dystrophy gene which greatly differs from the known isoforms in its structure and tissue distribution

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Characterization of a 4.8kb transcript from the Duchenne muscular dystrophy locus expressed in Schwannoma cells

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G-utrophin, the autosomal homologue of dystrophin Dp116, is expressed in sensory ganglia and brain.

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An alternative dystrophin transcript specific to peripheral nerve

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New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophin

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Distal transcript of the dystrophin gene initiated from an alternative first exon and encoding a 75-kDa protein widely distributed in nonmuscle tissues

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

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

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A 71-kilodalton protein is a major product of the Duchenne muscular dystrophy gene in brain and other nonmuscle tissues

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Tissue distribution of the dystrophin-related gene product and expression in the mdx and dy mouse

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Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle

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Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice

21 January 2018

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Apo-dystrophin-1 and apo-dystrophin-2, products of the Duchenne muscular dystrophy locus: expression during mouse embryogenesis and in cultured cell lines

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Primary structure of dystrophin-related protein

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Increasing complexity of the dystrophin-associated protein complex

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

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