Doublecortin facilitates the elongation of the somatic Golgi apparatus into proximal dendrites

Mutations in the doublecortin (DCX) gene, which encodes a microtubule (MT)-binding protein, cause human cortical malformations, including lissencephaly and subcortical band heterotopia. A deficiency in DCX and DCX-like kinase 1 (DCLK1), a functionally redundant and structurally similar cognate of DC...

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Detalles Bibliográficos
Autores principales: Li, Peijun, Li, Luyao, Yu, Binyuan, Wang, Xinye, Wang, Qi, Lin, Jingjing, Zheng, Yihui, Zhu, Jinjin, He, Minzhi, Xia, Zhaonan, Tu, Mengjing, Liu, Judy S., Lin, Zhenlang, Fu, Xiaoqin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2021
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8098852/
https://www.ncbi.nlm.nih.gov/pubmed/33405953
http://dx.doi.org/10.1091/mbc.E19-09-0530

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