Literature DB >> 7207483

DNA repair in Bloom's syndrome fibroblasts after UV irradiation or treatment with mitomycin C.

K Ishizaki, T Yagi, M Inoue, O Nikaido, H Takebe.   

Abstract

Sensitivities to UV and mitomycin C (MC) of fibroblasts obtained from 3 Japanese patients with Bloom's syndrome (BS) were studied. One BS strain was more sensitive to UV than normal cells only in colony-forming ability. Other responses to UV, such as unscheduled DNA synthesis, host-cell reactivation and removal of UV-endonuclease-susceptible sites, were normal in all 3 strains. These BS strains were more sensitive to MC than were normal cells. However, the amounts of unscheduled DNA synthesis after treatment with MC in BS cells did not differ from those in normal cells.

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Year:  1981        PMID: 7207483     DOI: 10.1016/0027-5107(81)90189-5

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


  9 in total

1.  A multiprotein nuclear complex connects Fanconi anemia and Bloom syndrome.

Authors:  Amom Ruhikanta Meetei; Salvatore Sechi; Michael Wallisch; Dafeng Yang; Mary K Young; Hans Joenje; Maureen E Hoatlin; Weidong Wang
Journal:  Mol Cell Biol       Date:  2003-05       Impact factor: 4.272

Review 2.  Human DNA repair defects.

Authors:  C F Arlett
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

3.  Evolution of the RECQ family of helicases: A drosophila homolog, Dmblm, is similar to the human bloom syndrome gene.

Authors:  K Kusano; M E Berres; W R Engels
Journal:  Genetics       Date:  1999-03       Impact factor: 4.562

4.  Presence of abnormally high incidences of sister chromatid exchanges in three successive cell cycles in Bloom's syndrome lymphocytes.

Authors:  H Tsuji; T Kojima
Journal:  Chromosoma       Date:  1985       Impact factor: 4.316

5.  Chromosomal breakage, endomitosis, endoreduplication, and hypersensitivity toward radiomimetric and alkylating agents: a possible new autosomal recessive mutation in a girl with craniosynostosis and microcephaly.

Authors:  N Tommerup; E Mortensen; M H Nielsen; R D Wegner; D Schindler; M Mikkelsen
Journal:  Hum Genet       Date:  1993-10       Impact factor: 4.132

6.  Bloom syndrome: a single complementation group defines patients of diverse ethnic origin.

Authors:  R Weksberg; C Smith; L Anson-Cartwright; K Maloney
Journal:  Am J Hum Genet       Date:  1988-06       Impact factor: 11.025

7.  Cell cycle parameters in radiation sensitive strains of Saccharomyces cerevisiae.

Authors:  R Fingerhut; J Kiefer; F Otto
Journal:  Mol Gen Genet       Date:  1984

8.  Bloom syndrome: an analysis of consanguineous families assigns the locus mutated to chromosome band 15q26.1.

Authors:  J German; A M Roe; M F Leppert; N A Ellis
Journal:  Proc Natl Acad Sci U S A       Date:  1994-07-05       Impact factor: 11.205

9.  Bloom syndrome complex promotes FANCM recruitment to stalled replication forks and facilitates both repair and traverse of DNA interstrand crosslinks.

Authors:  Chen Ling; Jing Huang; Zhijiang Yan; Yongjiang Li; Mioko Ohzeki; Masamichi Ishiai; Dongyi Xu; Minoru Takata; Michael Seidman; Weidong Wang
Journal:  Cell Discov       Date:  2016-12-20       Impact factor: 10.849

  9 in total

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