Literature DB >> 6206393

Evaluations of wasted mouse fibroblasts and SV-40 transformed human fibroblasts as models of ataxia telangiectasia in vitro.

S K Nordeen, V G Schaefer, M H Edgell, C A Hutchison, L D Shultz, M Swift.   

Abstract

Fibroblast cultures from wasted mice have been derived and the responses of these cultures to bleomycin treatment or gamma-irradiation have been examined. No differences were observed between wasted fibroblasts and littermate controls in the post-treatment inhibition of DNA replication. In contrast, a human SV-40 transformed ataxia telangiectasia fibroblast line mimicked the abnormal response of primary ataxia telangiectasia fibroblasts to gamma-rays or bleomycin and thus appears to be a useful in vitro model of ataxia telangiectasia.

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Year:  1984        PMID: 6206393     DOI: 10.1016/0165-7992(84)90081-2

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  2 in total

1.  The lethal mutation of the mouse wasted (wst) is a deletion that abolishes expression of a tissue-specific isoform of translation elongation factor 1alpha, encoded by the Eef1a2 gene.

Authors:  D M Chambers; J Peters; C M Abbott
Journal:  Proc Natl Acad Sci U S A       Date:  1998-04-14       Impact factor: 11.205

2.  Deficiency of adenosine deaminase in the wasted mouse.

Authors:  C M Abbott; C J Skidmore; A G Searle; J Peters
Journal:  Proc Natl Acad Sci U S A       Date:  1986-02       Impact factor: 11.205

  2 in total

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