Literature DB >> 1910092

Sister chromatid exchange evaluation as an aid to the diagnosis and exclusion of Fanconi's anaemia by induced chromosome damage analysis.

R T Howell1.   

Abstract

Evaluation of chromatid aberrations induced in culture by DNA cross linking agents provides the most reliable method currently available for the diagnosis and exclusion of Fanconi's anaemia. However, at appropriate concentrations of clastogenic agent the aberration frequency in an unaffected subject may be very low and thus it may be difficult to confirm that the treatment was effective. Data are presented to show that sister chromatid exchange analysis can be used to monitor the effectiveness of the clastogen treatment and thereby increase the reliability and efficiency of the assay.

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Year:  1991        PMID: 1910092      PMCID: PMC1016957          DOI: 10.1136/jmg.28.7.468

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  12 in total

1.  International Fanconi Anemia Registry: relation of clinical symptoms to diepoxybutane sensitivity.

Authors:  A D Auerbach; A Rogatko; T M Schroeder-Kurth
Journal:  Blood       Date:  1989-02       Impact factor: 22.113

2.  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

3.  Fanconi's anaemia in the genetics of neoplasia.

Authors:  M Swift
Journal:  Nature       Date:  1971-04-09       Impact factor: 49.962

4.  Prenatal and postnatal diagnosis and carrier detection of Fanconi anemia by a cytogenetic method.

Authors:  A D Auerbach; B Adler; R S Chaganti
Journal:  Pediatrics       Date:  1981-01       Impact factor: 7.124

5.  Cytological detection of mutagen-carcinogen exposure by sister chromatid exchange.

Authors:  P Perry; H J Evans
Journal:  Nature       Date:  1975-11-13       Impact factor: 49.962

6.  Chromosome abnormalities in constitutional aplastic anemia.

Authors:  G E Bloom; S Warner; P S Gerald; L K Diamond
Journal:  N Engl J Med       Date:  1966-01-06       Impact factor: 91.245

7.  Mitomycin C induced chromosome damage in fetal blood cultures and prenatal diagnosis of Fanconi's anaemia.

Authors:  J Shipley; C H Rodeck; C Garrett; J Galbraith; F Giannelli
Journal:  Prenat Diagn       Date:  1984 May-Jun       Impact factor: 3.050

8.  Clinical and cytogenetic diversity in Fanconi's anaemia.

Authors:  G Duckworth-Rysiecki; M Hultén; J Mann; A M Taylor
Journal:  J Med Genet       Date:  1984-06       Impact factor: 6.318

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.  Clastogen-induced chromosomal breakage as a marker for first trimester prenatal diagnosis of Fanconi anemia.

Authors:  A D Auerbach; Z Min; R Ghosh; E Pergament; Y Verlinsky; H Nicolas; J Boué
Journal:  Hum Genet       Date:  1986-05       Impact factor: 4.132

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  1 in total

1.  Reduced FANCD2 influences spontaneous SCE and RAD51 foci formation in uveal melanoma and Fanconi anaemia.

Authors:  P Gravells; L Hoh; S Solovieva; A Patil; E Dudziec; I G Rennie; K Sisley; H E Bryant
Journal:  Oncogene       Date:  2013-01-14       Impact factor: 9.867

  1 in total

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