Literature DB >> 648172

Fragility and spiralization anomalies of the chromosomes in three cases, including fraternal twins, with Fanconi's anemia, type Estren-Dameshek.

W Schmid, G Fanconi.   

Abstract

Fraternal twins, offspring of consanguineous parents, developed pancytopenia, the boy at 7, the girl at 12 years of age. A third patient became anemic at 3 years. All three are free of associated malformations. In blood cultures the incidence of chromatid breaks, exchanges, and chromosome-type aberrations was elevated to 24%, 18%, and 28%, respectively. In addition, in a low number of mitotic cells unusual observations, pointing to profound disturbances of chromosome structure, were made. It is suggested that these patients have a genetic defect impairing the normal process of mitotic chromosome condensation and decondensation.

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Year:  1978        PMID: 648172     DOI: 10.1159/000130845

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  7 in total

1.  Fanconi's anemia in monozygotic twins.

Authors:  Fulton D'Souza; M K Usha; S D Subba Rao
Journal:  Indian J Pediatr       Date:  2007-09       Impact factor: 1.967

2.  The behavior of allocyclic chromosomes in Bloom's syndrome.

Authors:  P G Otto; P A Otto; E Therman
Journal:  Chromosoma       Date:  1981       Impact factor: 4.316

3.  A genetic screen identifies FAN1, a Fanconi anemia-associated nuclease necessary for DNA interstrand crosslink repair.

Authors:  Agata Smogorzewska; Rohini Desetty; Takamune T Saito; Michael Schlabach; Francis P Lach; Mathew E Sowa; Alan B Clark; Thomas A Kunkel; J Wade Harper; Monica P Colaiácovo; Stephen J Elledge
Journal:  Mol Cell       Date:  2010-07-09       Impact factor: 17.970

4.  Familial thrombocytopenia associated with platelet autoantibodies and chromosome breakage.

Authors:  F M Helmerhorst; D C Heaton; P E Crossen; A E von dem Borne; C P Engelfriet; A T Natarajan
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

5.  Single-copy and amplified CAD genes in Syrian hamster chromosomes localized by a highly sensitive method for in situ hybridization.

Authors:  G M Wahl; L Vitto; R A Padgett; G R Stark
Journal:  Mol Cell Biol       Date:  1982-03       Impact factor: 4.272

6.  Defective mitochondrial peroxiredoxin-3 results in sensitivity to oxidative stress in Fanconi anemia.

Authors:  Sudit S Mukhopadhyay; Kathryn S Leung; M John Hicks; Philip J Hastings; Hagop Youssoufian; Sharon E Plon
Journal:  J Cell Biol       Date:  2006-10-23       Impact factor: 10.539

7.  Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair.

Authors:  Agata Smogorzewska; Shuhei Matsuoka; Patrizia Vinciguerra; E Robert McDonald; Kristen E Hurov; Ji Luo; Bryan A Ballif; Steven P Gygi; Kay Hofmann; Alan D D'Andrea; Stephen J Elledge
Journal:  Cell       Date:  2007-04-05       Impact factor: 41.582

  7 in total

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