Disease-associated mutations in human TUBB3 disturb netrin repulsive signaling

Missense mutations in the human TUBB3 gene cause a variety of neurological disorders associated with defects in axon guidance and neuronal migration, but the underlying molecular mechanisms are not well understood. Recent studies have shown that direct coupling of dynamic TUBB3 in microtubules with...

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Dades bibliogràfiques
Publicat a:PLoS One
Autors principals: Shao, Qiangqiang, Yang, Tao, Huang, Huai, Majumder, Tanushree, Khot, Bhakti Ajit, Khouzani, Mohammad Masoudian, Alarmanazi, Farrah, Gore, Yasmin K., Liu, Guofa
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2019
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6588280/
https://ncbi.nlm.nih.gov/pubmed/31226147
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0218811
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