Literature DB >> 19029913

Human embryonic stem cells reveal recurrent genomic instability at 20q11.21.

Nathalie Lefort1, Maxime Feyeux, Cécile Bas, Olivier Féraud, Annelise Bennaceur-Griscelli, Gerard Tachdjian, Marc Peschanski, Anselme L Perrier.   

Abstract

By analyzing five human embryonic stem (hES) cell lines over long-term culture, we identified a recurrent genomic instability in the human genome. An amplification of 2.5-4.6 Mb at 20q11.21, encompassing approximately 23 genes in common, was detected in four cell lines of different origins. This amplification, which has been associated with oncogenic transformation, may provide a selective advantage to hES cells in culture.

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Year:  2008        PMID: 19029913     DOI: 10.1038/nbt.1509

Source DB:  PubMed          Journal:  Nat Biotechnol        ISSN: 1087-0156            Impact factor:   54.908


  87 in total

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10.  Functional in vivo and in vitro effects of 20q11.21 genetic aberrations on hPSC differentiation.

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