Literature DB >> 6745925

Heterozygous carriers for Bloom syndrome exhibit a spontaneously increased micronucleus formation in cultured fibroblasts.

B Frorath, U Schmidt-Preuss, U Siemers, M Zöllner, H W Rüdiger.   

Abstract

Cultured fibroblasts of homozygotes and heterozygotes for Bloom syndrome exhibit an enhanced formation of micronuclei. The number of spontaneously occurring micronuclei permit clear separation of heterozygotes from either normal controls or homozygous patients without overlap between these groups. The observed differences could not be enhanced further by the addition of various mutagens. We conclude from the increased chromosomal damage that heterozygotes for Bloom syndrome may have a higher risk for malignant diseases.

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Year:  1984        PMID: 6745925     DOI: 10.1007/BF00270558

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


  24 in total

1.  CHROMOSOMAL BREAKAGE IN A RARE AND PROBABLY GENETICALLY DETERMINED SYNDROME OF MAN.

Authors:  J GERMAN; R ARCHIBALD; D BLOOM
Journal:  Science       Date:  1965-04-23       Impact factor: 47.728

2.  [Chemical mutagenesis in mammals. The Chinese hamster bone marrow as an in vivo test system. Hematological findings after treatment with trenimon].

Authors:  K Boller; W Schmid
Journal:  Humangenetik       Date:  1970

3.  A simple cytochemical technique for demonstration of DNA in cells infected with mycoplasmas and viruses.

Authors:  W C Russell; C Newman; D H Williamson
Journal:  Nature       Date:  1975-02-06       Impact factor: 49.962

4.  Response of lymphocytes from Fanconi's anemia patients and their heterozygous relatives to 8-methoxy-psoralene in a cloning survival test system.

Authors:  E Wunder; B Fleischer-Reischmann
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

5.  Functional deficiency of fibroblasts heterozygous for Bloom syndrome as specific manifestation of the primary defect.

Authors:  C R Bartram; H W Rüdiger; U Schmidt-Preuss; E Passarge
Journal:  Am J Hum Genet       Date:  1981-11       Impact factor: 11.025

6.  Malignant neoplasms in the families of patients with ataxia-telangiectasia.

Authors:  M Swift; L Sholman; M Perry; C Chase
Journal:  Cancer Res       Date:  1976-01       Impact factor: 12.701

7.  Mutagen-induced sister chromatid exchange rate in Bloom syndrome remains unaltered in the presence of Bloom corrective factor.

Authors:  U Schmidt-Preuss; P Maack; C R Bartram; H W Rüdiger
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

8.  Reassessment of cancer predisposition of Fanconi anemia heterozygotes.

Authors:  M Swift; R J Caldwell; C Chase
Journal:  J Natl Cancer Inst       Date:  1980-11       Impact factor: 13.506

9.  Genetic heterogeneity of Fanconi's anemia demonstrated by somatic cell hybrids.

Authors:  S Zakrzewski; K Sperling
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

10.  Sensitivity of Bloom's syndrome lymphocytes to ethyl methanesulfonate.

Authors:  A B Krepinsky; J A Heddle; J German
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

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  7 in total

1.  Evidence for increased in vivo mutation and somatic recombination in Bloom's syndrome.

Authors:  R G Langlois; W L Bigbee; R H Jensen; J German
Journal:  Proc Natl Acad Sci U S A       Date:  1989-01       Impact factor: 11.205

2.  Evidence for chromosome instability in vivo in Bloom syndrome: increased numbers of micronuclei in exfoliated cells.

Authors:  M P Rosin; J German
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

3.  Stage-specific apoptosis, developmental delay, and embryonic lethality in mice homozygous for a targeted disruption in the murine Bloom's syndrome gene.

Authors:  N Chester; F Kuo; C Kozak; C D O'Hara; P Leder
Journal:  Genes Dev       Date:  1998-11-01       Impact factor: 11.361

4.  Increased numbers of spontaneous micronuclei in blood lymphocytes and cultures fibroblasts of individuals with familial cutaneous malignant melanoma.

Authors:  M Weichenthal; M Roser; U Ehlert; S Frenzer; E Breitbart; H W Rüdiger
Journal:  J Cancer Res Clin Oncol       Date:  1989       Impact factor: 4.553

5.  A tri-serine cluster within the topoisomerase IIα-interaction domain of the BLM helicase is required for regulating chromosome breakage in human cells.

Authors:  Julia Harris Behnfeldt; Samir Acharya; Larissa Tangeman; April Sandy Gocha; Jeremy Keirsey; Joanna Groden
Journal:  Hum Mol Genet       Date:  2018-04-01       Impact factor: 6.150

Review 6.  RecQ helicases: suppressors of tumorigenesis and premature aging.

Authors:  Csanád Z Bachrati; Ian D Hickson
Journal:  Biochem J       Date:  2003-09-15       Impact factor: 3.857

7.  The cytogenetics of Bloom's syndrome.

Authors:  Ashish Singh; S Ambujam; A N Uma
Journal:  J Pediatr Neurosci       Date:  2010-07
  7 in total

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