Literature DB >> 492197

A seventh complementation group in excision-deficient xeroderma pigmentosum.

W Keijzer, N G Jaspers, P J Abrahams, A M Taylor, C F Arlett, B Zelle, H Takebe, P D Kinmont, D Bootsma.   

Abstract

Cells from a xeroderma pigmentosum patient XP2BI who has reached 17 years of age with no keratoses or skin tumours constitute a new, 7th complementation group G. These cells exhibit a low residual level of excision repair, 2% of normal after a UV dose of 5 J/m2 and an impairment of post-replication repair characteristic of excision-defective XPs. They are also sensitive to the lethal effects of UV and defective in host-cell reactivation of UV-irradiated SV40 DNA.

Entities:  

Mesh:

Substances:

Year:  1979        PMID: 492197     DOI: 10.1016/0027-5107(79)90231-8

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


  29 in total

1.  Mfd is required for rapid recovery of transcription following UV-induced DNA damage but not oxidative DNA damage in Escherichia coli.

Authors:  Brandy J Schalow; Charmain T Courcelle; Justin Courcelle
Journal:  J Bacteriol       Date:  2012-03-16       Impact factor: 3.490

2.  Complementation of the xeroderma pigmentosum DNA repair synthesis defect with Escherichia coli UvrABC proteins in a cell-free system.

Authors:  J Hansson; L Grossman; T Lindahl; R D Wood
Journal:  Nucleic Acids Res       Date:  1990-01-11       Impact factor: 16.971

3.  ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs.

Authors:  K W Brookman; J E Lamerdin; M P Thelen; M Hwang; J T Reardon; A Sancar; Z Q Zhou; C A Walter; C N Parris; L H Thompson
Journal:  Mol Cell Biol       Date:  1996-11       Impact factor: 4.272

4.  Complementation studies between Fanconi's anemia cells with different DNA repair characteristics.

Authors:  S Zakrzewski; M Koch; K Sperling
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

5.  Genetic heterogeneity in ataxia-telangiectasia studied by cell fusion.

Authors:  N G Jaspers; D Bootsma
Journal:  Proc Natl Acad Sci U S A       Date:  1982-04       Impact factor: 11.205

6.  Human chromosome 13 compensates a DNA repair defect in UV-sensitive mouse cells by mouse--human cell hybridization.

Authors:  T Hori; T Shiomi; K Sato
Journal:  Proc Natl Acad Sci U S A       Date:  1983-09       Impact factor: 11.205

7.  Clinical and biological studies of 26 cases of xeroderma pigmentosum in northeast district of Japan.

Authors:  T Kato; H Akiba; M Seiji; H Tohda; A Oikawa
Journal:  Arch Dermatol Res       Date:  1985       Impact factor: 3.017

8.  Formation of a ternary complex by human XPA, ERCC1, and ERCC4(XPF) excision repair proteins.

Authors:  C H Park; A Sancar
Journal:  Proc Natl Acad Sci U S A       Date:  1994-05-24       Impact factor: 11.205

Review 9.  XPG: its products and biological roles.

Authors:  Orlando D Schärer
Journal:  Adv Exp Med Biol       Date:  2008       Impact factor: 2.622

10.  Xeroderma pigmentosum patients from Germany: clinical symptoms and DNA repair characteristics.

Authors:  E Fischer; H W Thielmann; B Neundörfer; F J Rentsch; L Edler; E G Jung
Journal:  Arch Dermatol Res       Date:  1982       Impact factor: 3.017

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.