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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...
保存先:
| 出版年: | EMBO Rep |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BlackWell Publishing Ltd
2015
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| 主題: | |
| オンライン･アクセス: | 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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