Literature DB >> 3804331

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

E Moustacchi, D Papadopoulo, C Diatloff-Zito, M Buchwald.   

Abstract

The two genetic complementation groups reported for Fanconi's anemia (FA) correspond to two phenotypic classes as characterized by measurements of the rate of DNA semiconservative synthesis after 8-methoxypsoralen photoaddition. This test allows a rapid genetic classification of FA patients which appears to be a prerequisite for investigations of the biochemical defect(s) in FA.

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Year:  1987        PMID: 3804331     DOI: 10.1007/bf00273837

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


  25 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.  Susceptibility of Fanconi's anaemia fibroblasts to chromosome damage by carcinogens.

Authors:  A D Auerbach; S R Wolman
Journal:  Nature       Date:  1976-06-10       Impact factor: 49.962

3.  Effects of mitomycin C on the rate of DNA synthesis in normal and Fanconi anaemia cells.

Authors:  E Claassen; H Kortbeek; F Arwert
Journal:  Mutat Res       Date:  1986-01       Impact factor: 2.433

4.  A high susceptibility of Fanconi's anemia to chromosome breakage by DNA cross-linking agents.

Authors:  M S Sasaki; A Tonomura
Journal:  Cancer Res       Date:  1973-08       Impact factor: 12.701

5.  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

6.  Defective repair of mitomycin C crosslinks in Fanconi's anemia and loss in confluent normal human and xeroderma pigmentosum cells.

Authors:  Y Fujiwara
Journal:  Biochim Biophys Acta       Date:  1982-12-31

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.  Repair of psoralen adducts in human DNA: differences among xeroderma pigmentosum complementation groups.

Authors:  J E Cleaver; D C Gruenert
Journal:  J Invest Dermatol       Date:  1984-04       Impact factor: 8.551

9.  The cell cycle of lymphocytes in Fanconi anemia.

Authors:  B Dutrillaux; A Aurias; A M Dutrillaux; D Buriot; M Prieur
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

10.  DNA repair in a Fanconi's anemia fibroblast cell strain.

Authors:  A J Fornace; J B Little; R R Weichselbaum
Journal:  Biochim Biophys Acta       Date:  1979-01-26
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  11 in total

1.  Hypomutability in Fanconi anemia cells is associated with increased deletion frequency at the HPRT locus.

Authors:  D Papadopoulo; C Guillouf; H Mohrenweiser; E Moustacchi
Journal:  Proc Natl Acad Sci U S A       Date:  1990-11       Impact factor: 11.205

2.  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

3.  Abnormal lymphokine production: a novel feature of the genetic disease Fanconi anemia. I. Involvement of interleukin-6.

Authors:  F Rosselli; J Sanceau; J Wietzerbin; E Moustacchi
Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

4.  Subtyping analysis of Fanconi anemia by immunoblotting and retroviral gene transfer.

Authors:  M Pulsipher; G M Kupfer; D Naf; A Suliman; J S Lee; P Jakobs; M Grompe; H Joenje; C Sieff; E Guinan; R Mulligan; A D D'Andrea
Journal:  Mol Med       Date:  1998-07       Impact factor: 6.354

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

Authors:  M Digweed; S Zakrzewski-Lüdcke; K Sperling
Journal:  Hum Genet       Date:  1988-01       Impact factor: 4.132

6.  Cocultivation of Fanconi anemia cells and of mouse lymphoma mutants leads to interspecies complementation of chromosomal hypersensitivity to DNA cross-linking agents.

Authors:  F Rosselli; E Moustacchi
Journal:  Hum Genet       Date:  1990-05       Impact factor: 4.132

7.  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

8.  Molecular cloning of SNM1, a yeast gene responsible for a specific step in the repair of cross-linked DNA.

Authors:  E Haase; D Riehl; M Mack; M Brendel
Journal:  Mol Gen Genet       Date:  1989-07

9.  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

10.  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

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