Lis1 and doublecortin function with dynein to mediate coupling of the nucleus to the centrosome in neuronal migration

Autor: Tanaka, T, Serneo, F F, Higgins, C, Gambello, M J, Wynshaw-Boris, A, Gleeson, J G

Publikováno v: Tanaka, T; Serneo, F F; Higgins, C; Gambello, M J; Wynshaw-Boris, A; & Gleeson, J G. (2004). Lis1 and doublecortin function with dynein to mediate coupling of the nucleus to the centrosome in neuronal migration. Journal of Cell Biology, 165(5), 709-721. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/1sj2607t

Humans with mutations in either DCX or LIS1 display nearly identical neuronal migration defects, known as lissencephaly. To define subcellular mechanisms, we have combined in vitro neuronal migration assays with retroviral transduction. Overexpressio

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______325::9e5e287d71bf095f76c67290a6ebbf52
http://www.escholarship.org/uc/item/1sj2607t

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Pseudomonas aeruginosa LasA: a second elastase under the transcriptional control of lasR.

Autor: Toder, D. S., Gambello, M. J., Iglewski, B. H.

Publikováno v: Molecular Microbiology; Aug1991, Vol. 5 Issue 8, p2003-2010, 8p, 2 Black and White Photographs, 3 Diagrams, 2 Charts

Impaired learning and motor behavior in heterozygous Pafah1b1 (Lis1) mutant mice.

Autor: Paylor, R, Hirotsune, S, Gambello, M J, Yuva-Paylor, L, Crawley, J N, Wynshaw-Boris, A

Publikováno v: Learning & Memory; 1999, Vol. 6 Issue: 5 p521-537, 17p