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mNUDC is required for plus-end-directed transport of cytoplasmic dynein and dynactins by kinesin-1

Lissencephaly is a devastating neurological disorder caused by defective neuronal migration. The LIS1 (or PAFAH1B1) gene was identified as the gene mutated in lissencephaly patients, and was found to regulate cytoplasmic dynein function and localization. In particular, LIS1 is essential for anterogr...

詳細記述

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書誌詳細
主要な著者: Yamada, Masami, Toba, Shiori, Takitoh, Takako, Yoshida, Yuko, Mori, Daisuke, Nakamura, Takeshi, Iwane, Atsuko H, Yanagida, Toshio, Imai, Hiroshi, Yu-Lee, Li-yuan, Schroer, Trina, Wynshaw-Boris, Anthony, Hirotsune, Shinji
フォーマット: Artigo
言語:Inglês
出版事項: Nature Publishing Group 2010
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2830693/
https://ncbi.nlm.nih.gov/pubmed/20019668
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/emboj.2009.378
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