Literature DB >> 730181

The problem of partial endoreduplication.

C Stahl-Maugé, H D Hager, T M Schroeder.   

Abstract

Partial endoreduplication (PE) as defined by Lejeune et al. (1966) has only been found in a few instances. Similar configurations, also called PEs, seem to originate from a different process. A series of 12 PEs is presented in this paper, discovered in metaphases from healthy individuals, and in patients with or without chromosome-breakage syndrome and after treatment with chromosome-breaking agents. Interpretations of the microscopic appearance of each configuration led to the conclusion that there are three different modes of origin for such rare events, one being true partial endoreduplication, the second a partial pseudoendoreduplication, and the third a homologous triradial chromatid translocation.

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Year:  1978        PMID: 730181     DOI: 10.1007/bf00277573

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


  14 in total

1.  Inherited constriction fragility of chromosome 2.

Authors:  M A Ferguson-Smith
Journal:  Ann Genet       Date:  1973-03

2.  [Comparison of the structure of chromatids of Homo sapiens and Pan troglodytes (author's transl)].

Authors:  J Lejeune; B Dutrillaux; M O Rethoré; M Prieur
Journal:  Chromosoma       Date:  1973       Impact factor: 4.316

3.  Banding in human chromosomes treated with trypsin.

Authors:  H C Wang; S Fedoroff
Journal:  Nat New Biol       Date:  1972-01-12

4.  Bloom's syndrome and Fanconi's anemia: demonstration of two distinctive patterns of chromosome disruption and rearrangement.

Authors:  T M Schroeder; J German
Journal:  Humangenetik       Date:  1974

5.  [Selective endoreduplication of the long arm of the 2 chromosome in a woman and her daughter].

Authors:  J Lejeune; B Dutrillaux; J Lafourcade; R Berger; D Abonyi; M O Rethoré
Journal:  C R Acad Hebd Seances Acad Sci D       Date:  1968-01-03

6.  [On the selective endoreduplication of certain segments of the genome].

Authors:  J Lejeune; R Berger; M O Rethoré
Journal:  C R Acad Hebd Seances Acad Sci D       Date:  1966-12-07

7.  Heritable fragile site on chromosome 16: probable localization of haptoglobin locus in man.

Authors:  R E Magenis; F Hecht; E W Lovrien
Journal:  Science       Date:  1970-10-02       Impact factor: 47.728

8.  [A case of structural aberration of the chromosome A2].

Authors:  E Golob; E Kunze-Mühl; F Friedrich
Journal:  Humangenetik       Date:  1970-09-17

9.  Selective endoreduplication or branched chromosome?

Authors:  B Noël; B Quack; J Mottet; Y Nantois; B Dutrillaux
Journal:  Exp Cell Res       Date:  1977-02       Impact factor: 3.905

10.  [Selective endoreduplication of a supernumerary chromosome in a case of multiple myeloma (Kahler's disease)].

Authors:  J de Grouchy; C de Nava; G Bilski-Pasquier; R Zittoun; A Bernadou
Journal:  Ann Genet       Date:  1967-03
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  4 in total

Review 1.  Potential genetic functions of tandem repeated DNA sequence blocks in the human genome are based on a highly conserved "chromatin folding code".

Authors:  P Vogt
Journal:  Hum Genet       Date:  1990-03       Impact factor: 4.132

2.  Multibranched chromosomes 1, 9, and 16 in a patient with combined IgA and IgE deficiency.

Authors:  L Tiepolo; P Maraschio; G Gimelli; C Cuoco; G F Gargani; C Romano
Journal:  Hum Genet       Date:  1979-10-01       Impact factor: 4.132

3.  Origin of symmetrical triradial chromosomes in human cells.

Authors:  E M Kuhn; E Therman
Journal:  Chromosoma       Date:  1982       Impact factor: 4.316

4.  Chromosome breakage and rejoining of sister chromatids in Bloom's syndrome.

Authors:  E Meyer-Kuhn; E Therman
Journal:  Chromosoma       Date:  1979-08       Impact factor: 4.316

  4 in total

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