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Molecular Characterization of Down Syndrome Embryonic Stem Cells Reveals a Role for RUNX1 in Neural Differentiation
Down syndrome (DS) is the leading genetic cause of mental retardation and is caused by a third copy of human chromosome 21. The different pathologies of DS involve many tissues with a distinct array of neural phenotypes. Here we characterize embryonic stem cell lines with DS (DS-ESCs), and focus on...
Autores principales: | Halevy, Tomer, Biancotti, Juan-Carlos, Yanuka, Ofra, Golan-Lev, Tamar, Benvenisty, Nissim |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063584/ https://www.ncbi.nlm.nih.gov/pubmed/27618722 http://dx.doi.org/10.1016/j.stemcr.2016.08.003 |
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