Literature DB >> 1248828

Nonrandom distribution of chromosome breaks in cultured lymphocytes of normal subjects.

S Aymé, J F Mattei, M G Mattei, Y Aurran, F Giraud.   

Abstract

Breakpoint distribution was studied from cultured lymphocytes on 7653 metaphases from 524 subjects whose karyotypes were normal. The mean break rate was 5% in both sexes. The frequency increased significantly after 40 years and varied during the year. The location of the breaks was very different from the expected random distribution. The break frequency for each chromosome was different according to the type of break (chromatid, simple chromosomal and chromosomal involving rearrangements). The location of the breaks was also studied according to type of band and with respect to the centromere. A comparison between spontaneous breaks, X-ray induced breaks, breaks in Fanconi's anemia had in congenital rearrangements, show very significant differences.

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Year:  1976        PMID: 1248828     DOI: 10.1007/bf00296144

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


  10 in total

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Journal:  J Med Genet       Date:  1974-03       Impact factor: 6.318

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Journal:  Cytogenet Cell Genet       Date:  1973

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Journal:  Humangenetik       Date:  1974

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Journal:  Mutat Res       Date:  1973-06       Impact factor: 2.433

6.  High resolution studies on the pattern of induced exchanges in the human karyotype.

Authors:  M Seabright
Journal:  Chromosoma       Date:  1973       Impact factor: 4.316

7.  Radiation-induced non-random chromosome breakage.

Authors:  T Caspersson; U Haglund; B Lindell; L Zech
Journal:  Exp Cell Res       Date:  1972-12       Impact factor: 3.905

8.  Inter- and intrachromosomal distribution of achromatic lesions and chromatid breaks in human chromosomes.

Authors:  G Obe; H Lüers
Journal:  Mutat Res       Date:  1972-11       Impact factor: 2.433

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Journal:  Nature       Date:  1968-02-10       Impact factor: 49.962

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Authors:  P A Jacobs; W M Court BROWN
Journal:  Nature       Date:  1966-11-19       Impact factor: 49.962

  10 in total
  23 in total

1.  Determination of the number of conserved chromosomal segments between species.

Authors:  S Kumar; S R Gadagkar; A Filipski; X Gu
Journal:  Genetics       Date:  2001-03       Impact factor: 4.562

2.  Cartographic study: breakpoints in 1574 families carrying human reciprocal translocations.

Authors:  O Cohen; C Cans; M Cuillel; J L Gilardi; H Roth; M A Mermet; P Jalbert; J Demongeot
Journal:  Hum Genet       Date:  1996-05       Impact factor: 4.132

3.  Different DNA-PKcs functions in the repair of radiation-induced and spontaneous DSBs within interstitial telomeric sequences.

Authors:  Déborah Revaud; Luis M Martins; François D Boussin; Laure Sabatier; Chantal Desmaze
Journal:  Chromosoma       Date:  2011-02-26       Impact factor: 4.316

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Journal:  Hum Genet       Date:  1979-04-17       Impact factor: 4.132

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Authors:  M Kähkönen
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

Review 8.  Pericentric inversions. Problems and significance for clinical genetics.

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Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

9.  DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes.

Authors:  T W Glover; C Berger; J Coyle; B Echo
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

10.  A new inducible fragile site on chromosome 3(p14.2) in human lymphocytes.

Authors:  R D Wegner
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

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