Literature DB >> 3659917

Conservation of the Duchenne muscular dystrophy gene in mice and humans.

E P Hoffman1, A P Monaco, C C Feener, L M Kunkel.   

Abstract

A portion of the Duchenne muscular dystrophy (DMD) gene transcript from human fetal skeletal muscle and mouse adult heart was sequenced, representing approximately 25 percent of the total, 14-kb DMD transcript. The nucleic acid and predicted amino acid sequences from the two species are nearly 90 percent homologous. The amino acid sequence that is predicted from this portion of the DMD gene indicates that the protein product might serve a structural role in muscle, but the abundance and tissue distribution of the messenger RNA suggests that the DMD protein is not nebulin.

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Year:  1987        PMID: 3659917     DOI: 10.1126/science.3659917

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  59 in total

1.  Resting calcium concentrations in isolated skeletal muscle fibres of dystrophic mice.

Authors:  D A Williams; S I Head; A J Bakker; D G Stephenson
Journal:  J Physiol       Date:  1990-09       Impact factor: 5.182

Review 2.  The muscular dystrophies.

Authors:  V Dubowitz
Journal:  Postgrad Med J       Date:  1992-07       Impact factor: 2.401

3.  Inhibition of the IKK/NF-κB pathway by AAV gene transfer improves muscle regeneration in older mdx mice.

Authors:  Y Tang; D P Reay; M N Salay; M Y Mi; P R Clemens; D C Guttridge; P D Robbins; J Huard; B Wang
Journal:  Gene Ther       Date:  2010-08-19       Impact factor: 5.250

4.  Characterization of WWP1 protein expression in skeletal muscle of muscular dystrophy chickens.

Authors:  Michihiro Imamura; Akinori Nakamura; Hideyuki Mannen; Shin'ichi Takeda
Journal:  J Biochem       Date:  2015-08-26       Impact factor: 3.387

5.  Hexose transport in human myoblasts.

Authors:  O T Mesmer; T C Lo
Journal:  Biochem J       Date:  1989-08-15       Impact factor: 3.857

Review 6.  The Cinderella story of metabolic profiling: does metabolomics get to go to the functional genomics ball?

Authors:  Julian L Griffin
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2006-01-29       Impact factor: 6.237

7.  Dystrophin expression and genotypic analysis of two cases of benign X linked myopathy (McLeod's syndrome).

Authors:  N D Carter; J E Morgan; A P Monaco; M S Schwartz; S Jeffery
Journal:  J Med Genet       Date:  1990-06       Impact factor: 6.318

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

Authors:  V M Chapman; D R Miller; D Armstrong; C T Caskey
Journal:  Proc Natl Acad Sci U S A       Date:  1989-02       Impact factor: 11.205

9.  Sequence analysis of two exons from the murine dystrophin locus.

Authors:  M K Maconochie; S D Brown; A J Greenfield
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

10.  Dystrophin As a Molecular Shock Absorber.

Authors:  Shimin Le; Miao Yu; Ladislav Hovan; Zhihai Zhao; James Ervasti; Jie Yan
Journal:  ACS Nano       Date:  2018-11-27       Impact factor: 15.881

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