Literature DB >> 69603

Localization chromatid breaks in Fanconi's anemia, using three consecutive stains.

B Dutrillaux, J Couturier, E Viegas-Péquignot, G Schaison.   

Abstract

The location of 339 break points was analyzed in three patients with Fanconi's anemia, using three consecutive stains: ordinary Giemsa, Q-banding, and R-banding. Almost all the breaks seem to take place in the Q bands, using R-banding, and in the R bands, using Q-banding. A very important artifact, varying according to the method used, is thus demonstrated. In fact, the breaks take place in the interbands, between R and Q bands. The breaks were also localized in relation to sister chromatid exchanges (SCEs), seen after BUDR treatment. There is a clear excess of breaks at place of SCE (29%). This may indicate a possible correlation between breaks and SCEs.

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Year:  1977        PMID: 69603     DOI: 10.1007/BF00293773

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


  18 in total

1.  The rate of sister chromatid exchanges parallel to spontaneous chromosome breakage in Fanconi's anemia and to trenimon-induced aberrations in human lymphocytes and fibroblasts.

Authors:  K Hayashi; W Schmid
Journal:  Humangenetik       Date:  1975-09-23

2.  Induction by alkylating agents of sister chromatid exchanges and chromatid breaks in Fanconi's anemia.

Authors:  S A Latt; G Stetten; L A Juergens; G R Buchanan; P S Gerald
Journal:  Proc Natl Acad Sci U S A       Date:  1975-10       Impact factor: 11.205

3.  Nonrandom distribution of chromosome breaks in Fanconi's anemia.

Authors:  H Von Koskull; P Aula
Journal:  Cytogenet Cell Genet       Date:  1973

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

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

5.  Preferential location of x-ray induced chromosome breakage in the R-bands of human chromosomes.

Authors:  M Holmberg; J Jonasson
Journal:  Hereditas       Date:  1973       Impact factor: 3.271

6.  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

7.  Giemsa technique for the detection of sister chromatid exchanges.

Authors:  J R Korenberg; E F Freedlender
Journal:  Chromosoma       Date:  1974       Impact factor: 4.316

8.  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

9.  [Cytogenetic and cytologic findings in enzymopenic panmyelopathies and pancytopenias. Familial myelopathy of Fanconi, glutathione-reductase deficiency anemia and megaloblastic B12 deficiency anemia].

Authors:  T M Schroeder
Journal:  Humangenetik       Date:  1966

10.  Familial constitutional panmyelocytopathy, Fanconi's anemia (F.A.). II. A discussion of the cytogenetic findings in Fanconi's anemia.

Authors:  W Schmid
Journal:  Semin Hematol       Date:  1967-07       Impact factor: 3.851

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  14 in total

1.  Premature condensation induces breaks at the interface of early and late replicating chromosome bands bearing common fragile sites.

Authors:  Eliane El Achkar; Michelle Gerbault-Seureau; Martine Muleris; Bernard Dutrillaux; Michelle Debatisse
Journal:  Proc Natl Acad Sci U S A       Date:  2005-12-05       Impact factor: 11.205

Review 2.  Chromosome bands, their chromatin flavors, and their functional features.

Authors:  G P Holmquist
Journal:  Am J Hum Genet       Date:  1992-07       Impact factor: 11.025

Review 3.  Genetics of neoplasia--impact of ecogenetics on oncogenesis. A review.

Authors:  D T Purtilo; L Paquin; T Gindhart
Journal:  Am J Pathol       Date:  1978-06       Impact factor: 4.307

4.  The constitutional fragility of chromosome 12 in a case of 46,XX,var(12)(gh',RHG,CAG,CBG).

Authors:  E Donti; G Venti; V Bocchini; G Rosi; R Armellini; N Trabalza
Journal:  Hum Genet       Date:  1979-04-17       Impact factor: 4.132

5.  Isoacentric and isocentric chromosomes originating after deletions of human chromosomes.

Authors:  B Dutrillaux; W Al Achkar; R Aledo; A Aurias; J Couturier; A M Dutrillaux; A Flüry-Herard; M Gerbault-Seureau; F Hoffschir; E Lamoliatte
Journal:  Hum Genet       Date:  1987-07       Impact factor: 4.132

6.  Sister chromatid exchanges and heterochromatin.

Authors:  I Schubert; R Rieger
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

7.  Prevention of chromosomal breakage in Fanconi's anemia by cocultivation with normal cells.

Authors:  I Nordenson; B Björksten; B Lundh
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

8.  Spectrum of anomalies in Fanconi anaemia.

Authors:  A Glanz; F C Fraser
Journal:  J Med Genet       Date:  1982-12       Impact factor: 6.318

9.  Analysis of a BrdU-sensitive site in the cactus mouse (Peromyscus eremicus): chromosomal breakage and sister-chromatid exchange.

Authors:  N R Schneider; R S Chaganti; J German
Journal:  Chromosoma       Date:  1980       Impact factor: 4.316

10.  Systematic analysis of 95 reciprocal translocations of autosomes.

Authors:  A Aurias; M Prieur; B Dutrillaux; J Lejeune
Journal:  Hum Genet       Date:  1978-12-29       Impact factor: 4.132

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