Literature DB >> 3338794

Fanconi's anaemia: correlation of genetic complementation group with psoralen/UVA response.

M Digweed1, S Zakrzewski-Lüdcke, K Sperling.   

Abstract

The correlation found by Moustacchi (1987) between cellular response to a crosslinking challenge and genetic heterogeneity in Fanconi's anaemia is confirmed for an earlier set of complementation groups (Zakrzewski and Sperling 1980). This allows the matching of the two independently established complementation groupings and better characterization of their DNA repair-related biochemical properties.

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Year:  1988        PMID： 3338794     DOI： 10.1007/bf00291234

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  21 in total

1.  Cross-link repair in human cells and its possible defect in Fanconi's anemia cells.

Authors:  Y Fujiwara; M Tatsumi
Journal:  J Mol Biol       Date:  1977-07-15       Impact factor: 5.469

2.  Formal genetics of Fanconi's anemia.

Authors:  T M Schroeder; D Tilgen; J Krüger; F Vogel
Journal:  Hum Genet       Date:  1976-06-29       Impact factor: 4.132

3.  Two complementation groups of Fanconi's anemia differ in their phenotypic response to a DNA-crosslinking treatment.

Authors:  E Moustacchi; D Papadopoulo; C Diatloff-Zito; M Buchwald
Journal:  Hum Genet       Date:  1987-01       Impact factor: 4.132

4.  Repair of psoralen-induced cross-links and monoadducts in normal and repair-deficient human fibroblasts.

Authors:  D C Gruenert; J E Cleaver
Journal:  Cancer Res       Date:  1985-11       Impact factor: 12.701

5.  Analysis of heterogeneity in Fanconi's anemia patients of different ethnic origin.

Authors:  S Zakrzewski; K Sperling
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

6.  Deficiency of DNA ligase activity in Fanconi's anemia.

Authors:  M Hirsch-Kauffmann; M Schweiger; E F Wagner; K Sperling
Journal:  Hum Genet       Date:  1978-11-24       Impact factor: 4.132

7.  DNA repair in human cells containing photoadducts of 8-methoxypsoralen or angelicin.

Authors:  J Kaye; C A Smith; P C Hanawalt
Journal:  Cancer Res       Date:  1980-03       Impact factor: 12.701

8.  Rejoining of DNA double-strand breaks in human fibroblasts and its impairment in one ataxia telangiectasia and two Fanconi strains.

Authors:  T M Coquerelle; K F Weibezahn
Journal:  J Supramol Struct Cell Biochem       Date:  1981

9.  Genetic heterogeneity of Fanconi's anemia demonstrated by somatic cell hybrids.

Authors:  S Zakrzewski; K Sperling
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

10.  DNA repair dependent NAD+ metabolism is impaired in cells from patients with Fanconi's anemia.

Authors:  H Klocker; B Auer; M Hirsch-Kauffmann; H Altmann; H J Burtscher; M Schweiger
Journal:  EMBO J       Date:  1983       Impact factor: 11.598
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  4 in total

1.  Partial complementation of the Fanconi anemia defect upon transfection by heterologous DNA. Phenotypic dissociation of chromosomal and cellular hypersensitivity to DNA cross-linking agents.

Authors:  C Diatloff-Zito; F Rosselli; J Heddle; E Moustacchi
Journal:  Hum Genet       Date:  1990-12       Impact factor: 4.132

2.  Irreversible repression of DNA synthesis in Fanconi anemia cells is alleviated by the product of a novel cyclin-related gene.

Authors:  M Digweed; U Günthert; R Schneider; H Seyschab; R Friedl; K Sperling
Journal:  Mol Cell Biol       Date:  1995-01       Impact factor: 4.272

3.  Localization of Fanconi anemia C protein to the cytoplasm of mammalian cells.

Authors:  H Youssoufian
Journal:  Proc Natl Acad Sci U S A       Date:  1994-08-16       Impact factor: 11.205

4.  A damage-recognition protein which binds to DNA containing interstrand cross-links is absent or defective in Fanconi anemia, complementation group A, cells.

Authors:  B Hang; A T Yeung; M W Lambert
Journal:  Nucleic Acids Res       Date:  1993-09-11       Impact factor: 16.971
  4 in total

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