Literature DB >> 2693617

Dystrophin in skeletal muscle. I. Western blot analysis using a monoclonal antibody.

L V Nicholson1, K Davison, G Falkous, C Harwood, E O'Donnell, C R Slater, J B Harris.   

Abstract

The value of analysing dystrophin on Western blots of skeletal muscle for the differential diagnosis of Xp21 muscular dystrophies is now fairly well established. Here we describe a sensitive system based on monoclonal antibodies to dystrophin. The specificity of the antibodies was established and experiments were undertaken to identify the source of dystrophin-related protein bands which were detected on blots of normal skeletal muscle. These investigations formed a necessary preliminary study to the application of the assay to samples of muscle obtained at biopsy from patients with Duchenne and Becker muscular dystrophy.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2693617     DOI: 10.1016/0022-510x(89)90223-2

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  59 in total

1.  Physiological characterization of muscle strength with variable levels of dystrophin restoration in mdx mice following local antisense therapy.

Authors:  Paul S Sharp; Hema Bye-a-Jee; Dominic J Wells
Journal:  Mol Ther       Date:  2010-10-05       Impact factor: 11.454

2.  Muscle fibre breakdown in venom-induced muscle degeneration.

Authors:  J B Harris; R Vater; M Wilson; M J Cullen
Journal:  J Anat       Date:  2003-04       Impact factor: 2.610

Review 3.  Molecular biology of neurological diseases.

Authors:  W J Cumming
Journal:  Postgrad Med J       Date:  1992-04       Impact factor: 2.401

Review 4.  Genetic and clinical correlations of Xp21 muscular dystrophy.

Authors:  K M Bushby
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

5.  Are cysteine-rich and COOH-terminal domains of dystrophin critical for sarcolemmal localization?

Authors:  D Récan; P Chafey; F Leturcq; J P Hugnot; N Vincent; F Tomé; H Collin; D Simon; P Czernichow; L V Nicholson
Journal:  J Clin Invest       Date:  1992-02       Impact factor: 14.808

6.  A normal male with an inherited deletion of one exon within the DMD gene.

Authors:  M Nordenskjöld; L Nicholson; L Edström; M Anvret; M Eiserman; C Slater; L Stolpe
Journal:  Hum Genet       Date:  1990-01       Impact factor: 4.132

7.  Immunoblot analysis of sarcoplasmic calcium binding proteins in Duchenne muscular dystrophy.

Authors:  I Niebrój-Dobosz; M Lukasiuk
Journal:  J Neurol       Date:  1995-01       Impact factor: 4.849

8.  Point mutations in the dystrophin gene.

Authors:  R G Roberts; M Bobrow; D R Bentley
Journal:  Proc Natl Acad Sci U S A       Date:  1992-03-15       Impact factor: 11.205

9.  Abnormal dystrophin expression in patients with limb girdle syndromes.

Authors:  S Beyenburg; S Zierz; K Arahata; R R Mundegar; W Friedl; F Jerusalem
Journal:  J Neurol       Date:  1994-02       Impact factor: 4.849

10.  Functional significance of dystrophin positive fibres in Duchenne muscular dystrophy.

Authors:  L V Nicholson; M A Johnson; K M Bushby; D Gardner-Medwin
Journal:  Arch Dis Child       Date:  1993-05       Impact factor: 3.791

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.