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Stem and progenitor cell dysfunction in human trisomies

Trisomy 21, the commonest constitutional aneuploidy in humans, causes profound perturbation of stem and progenitor cell growth, which is both cell context dependent and developmental stage specific and mediated by complex genetic mechanisms beyond increased Hsa21 gene dosage. While proliferation of...

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Bibliografiske detaljer
Udgivet i:EMBO Rep
Main Authors: Liu, Binbin, Filippi, Sarah, Roy, Anindita, Roberts, Irene
Format: Artigo
Sprog:Inglês
Udgivet: BlackWell Publishing Ltd 2015
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4304728/
https://ncbi.nlm.nih.gov/pubmed/25520324
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15252/embr.201439583
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