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

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

Cloning and characterization of the Pseudomonas aeruginosa lasR gene, a transcriptional activator of elastase expression

Autor: Gambello, M J, Iglewski, B H

Publikováno v: Journal of Bacteriology; May 1991, Vol. 173 Issue: 9 p3000-3009, 10p

Primrose syndrome: Characterization of the phenotype in42 patients

Autor: Erica H. Gerkes, Pietro Strisciuglio, Renata Lazari Sandoval, Todd Waters, A. Rossi, Renata Posmyk, Sheela Unger, Constance T. R. M. Stumpel, Hanne B Hove, Tina Barbaro-Dieber, Marco Tartaglia, Keri Ramsey, Petr E. Jira, Daniel R. Carvalho, Vinodh Narayanan, Leonie A. Menke, Katherine Lachlan, Michael J. Gambello, Viviana Cordeddu, Sandra Jansen, Marrit M. Hitzert, Peter D. Turnpenny, Blanca Gener, Daniela Melis, Raoul C.M. Hennekam, Damara Ortiz, Clare Turnbull, Kyra E. Stuurman, Eline Overwater, Alberto J. Espay

Publikováno v: Clinical Genetics, 97(6), 890-901. Wiley-Blackwell
Clinical Genetics
Clinical Genetics, 97(6), 890-901. Wiley-Blackwell Publishing Ltd
Clinical Genetics, 97(6), 890-901. Wiley
Clinical genetics, 97(6), 890-901. Wiley-Blackwell
Melis, D, Carvalho, D, Barbaro-Dieber, T, Espay, A J, Gambello, M J, Gener, B, Gerkes, E, Hitzert, M M, Hove, H B, Jansen, S, Jira, P E, Lachlan, K, Menke, L A, Narayanan, V, Ortiz, D, Overwater, E, Posmyk, R, Ramsey, K, Rossi, A, Sandoval, R L, Stumpel, C, Stuurman, K E, Cordeddu, V, Turnpenny, P, Strisciuglio, P, Tartaglia, M, Unger, S, Waters, T, Turnbull, C & Hennekam, R C 2020, ' Primrose syndrome : Characterization of the phenotype in 42 patients ', Clinical Genetics, vol. 97, no. 6, pp. 890-901 . https://doi.org/10.1111/cge.13749
Clinical genetics, vol. 97, no. 6, pp. 890-901

Primrose syndrome (PS; MIM# 259050) is characterized by intellectual disability (ID), macrocephaly, unusual facial features (frontal bossing, deeply set eyes, down‐slanting palpebral fissures), calcified external ears, sparse body hair and distal m

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25c704da4b2a461a7f3c66ca7f294abe
http://hdl.handle.net/11386/4745225