Neonatal Tbr1 Dosage Controls Cortical Layer 6 Connectivity.

An understanding of how heterozygous loss-of-function mutations in ASD risk genes, such as TBR1, contribute to ASD remains elusive. Conditional Tbr1 deletion during late mouse gestation in cortical layer 6 neurons (Tbr1(layer6) mutants) provides novel insights into its function, including dendritic...

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Detaylı Bibliyografya
Yayımlandı:Neuron
Asıl Yazarlar: Siavash, Fazel Darbandi, Robinson Schwartz, Sarah E, Qihao, Qi, Rinaldo, Catta-Preta, Lin-Ling, Pai Emily, Mandell, Jeffrey D, Amanda, Everitt, Anna, Rubin, Krasnoff, Rebecca, A, Sol, Katzman, David, Tastad, Nord, Alex S, Jeremy, Willsey A., Bin, Chen, State, Matthew W., Sohal, Vikaas S, Rubenstein, John L. R
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2018
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6250594/
https://ncbi.nlm.nih.gov/pubmed/30318412
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuron.2018.09.027
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