Literature DB >> 1222585

Variegated translocation mosaicism in human skin fibroblast cultures.

H Hoehn, E M Bryant, K Au, T H Norwood, H Boman, G M Martin.   

Abstract

The term "variegated translocation mosaicism" is used to describe the repeated occurrence, within cultures of human skin fibroblasts, of a multiplicity of chromosomal rearrangements. With respect to the frequencies of such cytogenetically aberrant clones we found that they (1) were not detectable in routine diagnostic skin fibroblast cultures from 29 subjects with a wide variety of indications for biopsy; (2) were not detectable during in vitro aging of diploid strains with four normal individuals; (3) could be detected after rescue from bacterial contamination of a culture from an otherwise normal diploid male; (4) occurred with high frequencies in independent cultures from another apparently normal subject; (5) occurred with high frequencies in multiple biopsies obtained at autopsy from a patient with Werner's syndrome who died of sepsis; (6) were of pseudodiploid nature; and (7) involved a different spectrum of chromosomes in different individuals. A consistent association with mycoplasma contamination could not be made.

Entities:  

Mesh:

Substances:

Year:  1975        PMID: 1222585     DOI: 10.1159/000130526

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


  41 in total

Review 1.  Hutchinson-Guilford progeria syndrome.

Authors:  P K Sarkar; R A Shinton
Journal:  Postgrad Med J       Date:  2001-05       Impact factor: 2.401

2.  Mutations in the WRN gene in mice accelerate mortality in a p53-null background.

Authors:  D B Lombard; C Beard; B Johnson; R A Marciniak; J Dausman; R Bronson; J E Buhlmann; R Lipman; R Curry; A Sharpe; R Jaenisch; L Guarente
Journal:  Mol Cell Biol       Date:  2000-05       Impact factor: 4.272

3.  Abnormal skin fibroblast cytogenetics in four dysmorphic patients with normal lymphocyte chromosomes.

Authors:  R A Pagon; J G Hall; S L Davenport; J Aase; T H Norwood; H W Hoehn
Journal:  Am J Hum Genet       Date:  1979-01       Impact factor: 11.025

4.  Clinical utility gene card for: Werner syndrome.

Authors:  Fuki M Hisama; Christian Kubisch; George M Martin; Junko Oshima
Journal:  Eur J Hum Genet       Date:  2012-01-18       Impact factor: 4.246

Review 5.  The Werner mutation: does it lead to a "public" or "private" mechanism of aging?

Authors:  G M Martin
Journal:  Mol Med       Date:  1997-06       Impact factor: 6.354

6.  Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group.

Authors:  C E Yu; J Oshima; E M Wijsman; J Nakura; T Miki; C Piussan; S Matthews; Y H Fu; J Mulligan; G M Martin; G D Schellenberg
Journal:  Am J Hum Genet       Date:  1997-02       Impact factor: 11.025

Review 7.  Review of How Genetic Research on Segmental Progeroid Syndromes Has Documented Genomic Instability as a Hallmark of Aging But Let Us Now Pursue Antigeroid Syndromes!

Authors:  George M Martin; Fuki M Hisama; Junko Oshima
Journal:  J Gerontol A Biol Sci Med Sci       Date:  2021-01-18       Impact factor: 6.053

Review 8.  Genetics and the pathobiology of ageing.

Authors:  G M Martin
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1997-12-29       Impact factor: 6.237

9.  Effects of radical-scavenging enzymes and reduced oxygen exposure on growth and chromosome abnormalities of Werner syndrome cultured skin fibroblasts.

Authors:  D Salk; K Au; H Hoehn; G M Martin
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

10.  Role of SGS1 and SLX4 in maintaining rDNA structure in Saccharomyces cerevisiae.

Authors:  Vivek Kaliraman; Steven J Brill
Journal:  Curr Genet       Date:  2002-08-22       Impact factor: 3.886

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.