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Role of dynein, dynactin, and CLIP-170 interactions in LIS1 kinetochore function
Mutations in the human LIS1 gene cause type I lissencephaly, a severe brain developmental disease involving gross disorganization of cortical neurons. In lower eukaryotes, LIS1 participates in cytoplasmic dynein-mediated nuclear migration. We previously reported that mammalian LIS1 functions in cell...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Rockefeller University Press
2002
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2173479/ https://ncbi.nlm.nih.gov/pubmed/11889140 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1083/jcb.200109046 |
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