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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...
| Autores principales: | , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
The Rockefeller University Press
2002
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173479/ https://www.ncbi.nlm.nih.gov/pubmed/11889140 http://dx.doi.org/10.1083/jcb.200109046 |