Literature DB >> 3042661

Molecular genetics of Duchenne and Becker muscular dystrophy.

R G Worton1, A H Burghes.   

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Year:  1988        PMID： 3042661     DOI： 10.1016/s0074-7742(08)60083-5

Source DB:  PubMed          Journal:  Int Rev Neurobiol        ISSN： 0074-7742            Impact factor:   3.230


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  5 in total

1.  Carrier estimations in Duchenne muscular dystrophy families in Northern Ireland using RFLP analysis.

Authors:  E D Kelly; C A Graham; A J Hill; N C Nevin
Journal:  J Med Genet       Date:  1990-02       Impact factor: 6.318

2.  Lack of dystrophin but normal calcium homeostasis in smooth muscle from dystrophic mdx mice.

Authors:  B Boland; B Himpens; R Casteels; J M Gillis
Journal:  J Muscle Res Cell Motil       Date:  1993-02       Impact factor: 2.698

3.  Evidence for mutation by unequal sister chromatid exchange in the Duchenne muscular dystrophy gene.

Authors:  X Y Hu; A H Burghes; D E Bulman; P N Ray; R G Worton
Journal:  Am J Hum Genet       Date:  1989-06       Impact factor: 11.025

4.  Frameshift deletions of exons 3-7 and revertant fibers in Duchenne muscular dystrophy: mechanisms of dystrophin production.

Authors:  A V Winnard; J R Mendell; T W Prior; J Florence; A H Burghes
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

5.  Ixazomib, an oral proteasome inhibitor, exhibits potential effect in dystrophin-deficient mdx mice.

Authors:  Maria Laura Jorge Micheletto; Tulio de Almeida Hermes; Bruno Machado Bertassoli; Giuliana Petri; Matheus Moreira Perez; Fernando Luiz Affonso Fonseca; Alzira Alves de Siqueira Carvalho; David Feder
Journal:  Int J Exp Pathol       Date:  2020-12-09       Impact factor: 1.925
  5 in total

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