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High-Resolution Epigenomic Atlas of Human Embryonic Craniofacial Development

Defects in patterning during human embryonic development frequently result in craniofacial abnormalities. The gene regulatory programs that build the craniofacial complex are likely controlled by information located between genes and within intronic sequences. However, systematic identification of r...

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Podrobná bibliografie
Vydáno v:Cell Rep
Hlavní autoři: Wilderman, Andrea, VanOudenhove, Jennifer, Kron, Jeffrey, Noonan, James P., Cotney, Justin
Médium: Artigo
Jazyk:Inglês
Vydáno: 2018
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5965702/
https://ncbi.nlm.nih.gov/pubmed/29719267
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.celrep.2018.03.129
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