(Q48123207)

8 February 2018

title

New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophin. (English)

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8 February 2018

author name string

Cox GA

1

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8 February 2018

Phelps SF

2

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8 February 2018

Chapman VM

3

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8 February 2018

Chamberlain JS

4

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8 February 2018

language of work or name

English

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publication date

1 May 1993

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8 February 2018

published in

Nature Genetics

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8 February 2018

volume

4

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8 February 2018

page(s)

87-93

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8 February 2018

issue

1

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8 February 2018

https://scigraph.springernature.com/pub.10.1038/ng0593-87

exact match

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cites work

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

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Duchenne muscular dystrophy gene product is not identical in muscle and brain.

21 January 2018

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21 January 2018

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Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes

21 January 2018

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Expression of recombinant dystrophin and its localization to the cell membrane

21 January 2018

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Multiple cis-acting sequence elements are required for efficient splicing of simian virus 40 small-t antigen pre-mRNA

21 January 2018

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Scanning from an independently specified branch point defines the 3' splice site of mammalian introns

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Transcriptional regulation of the muscle creatine kinase gene and regulated expression in transfected mouse myoblasts

21 January 2018

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A new, simple myelin stain

21 January 2018

1 reference

Alternative splicing of human dystrophin mRNA generates isoforms at the carboxy terminus

21 January 2018

1 reference

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

21 January 2018

1 reference

The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy

21 January 2018

1 reference

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

21 January 2018

1 reference

7 January 2021

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

1 reference

7 January 2021

X chromosome-linked muscular dystrophy (mdx) in the mouse

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7 January 2021

Expression of the murine Duchenne muscular dystrophy gene in muscle and brain.

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7 January 2021

The molecular basis of muscular dystrophy in the mdx mouse: a point mutation

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7 January 2021

Human and murine dystrophin mRNA transcripts are differentially expressed during skeletal muscle, heart, and brain development

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7 January 2021

Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice

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7 January 2021

PCR analysis of dystrophin gene mutation and expression

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7 January 2021

Determination of the exon structure of the distal portion of the dystrophin gene by vectorette PCR.

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7 January 2021

The frequency of revertants in mdx mouse genetic models for Duchenne muscular dystrophy

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7 January 2021

Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy

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7 January 2021

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

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7 January 2021

Increased activity of calcium leak channels in myotubes of Duchenne human and mdx mouse origin

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7 January 2021

Is the carboxyl-terminus of dystrophin required for membrane association? A novel, severe case of duchenne muscular dystrophy

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7 January 2021

Point mutations in the dystrophin gene

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7 January 2021

Characterization of patients with glycerol kinase deficiency utilizing cDNA probes for the Duchenne muscular dystrophy locus

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7 January 2021

Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

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7 January 2021

Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer

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7 January 2021

Dystrophin expression and somatic reversion in prednisone-treated and untreated Duchenne dystrophy. CIDD Study Group

1 reference

7 January 2021

Sequence analysis of two exons from the murine dystrophin locus.

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG0593-87

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8 February 2018

PubMed ID

8099842

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8 February 2018