Nipbl Interacts with Zfp609 and the Integrator Complex to Regulate Cortical Neuron Migration

Mutations in NIPBL are the most frequent cause of Cornelia de Lange syndrome (CdLS), a developmental disorder encompassing several neurological defects, including intellectual disability and seizures. How NIPBL mutations affect brain development is not understood. Here we identify Nipbl as a functio...

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Detaylı Bibliyografya
Yayımlandı:Neuron
Asıl Yazarlar: van den Berg, Debbie L.C., Azzarelli, Roberta, Oishi, Koji, Martynoga, Ben, Urbán, Noelia, Dekkers, Dick H.W., Demmers, Jeroen A., Guillemot, François
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Cell Press 2017
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5263256/
https://ncbi.nlm.nih.gov/pubmed/28041881
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuron.2016.11.047
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