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Essential Roles for ARID1B in Dendritic Arborization and Spine Morphology of Developing Pyramidal Neurons

De novo truncating mutations in ARID1B, a chromatin-remodeling gene, cause Coffin–Siris syndrome, a developmental disorder characterized by intellectual disability and speech impairment; however, how the genetic elimination leads to cognitive dysfunction remains unknown. Thus, we investigated the ne...

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Detalhes bibliográficos
Publicado no:J Neurosci
Main Authors: Ka, Minhan, Chopra, Divyan A., Dravid, Shashank M., Kim, Woo-Yang
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4879215/
https://ncbi.nlm.nih.gov/pubmed/26937011
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.2321-15.2016
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