ASPM is a major determinant of cerebral cortical size (original) (raw)
References
Aicardi, J. Diseases of the Nervous System in Childhood edn 2, 90–91 (MacKeith, London, 1998). Google Scholar
Pattison, L. et al. A fifth locus for primary autosomal recessive microcephaly maps to chromosome 1q31. Am. J. Hum. Genet.67, 1578–1580 (2000). ArticleCAS Google Scholar
Jamieson, C.R., Fryns, J.P., Jacobs, J., Matthijs, G. & Abramowicz, M.J. Primary autosomal recessive microcephaly: MCPH5 maps to 1q25–q32. Am. J. Hum. Genet.67, 1575–1577 (2000). ArticleCAS Google Scholar
Bundey, S. in Emery and Rimoin's Principles and Practice of Medical Genetics 3rd edn (eds Rimoin, D.L., Connor, J.M. & Pyeritz, R.E.) 730–731 (Churchill Livingstone, New York, 1997). Google Scholar
Ripoll, P., Pimpinelli, S., Valdivia, M.M. & Avila, J. A cell division mutant of Drosophila with a functionally abnormal spindle. Cell41, 907–912 (1985).
Gonzalez, C. et al. Mutations at the asp locus of Drosophila lead to multiple free centrosomes in syncytial embryos, but restrict centrosome duplication in larval neuroblasts. J. Cell Sci.96, 605–616 (1990). PubMed Google Scholar
Mochida, G.H. & Walsh, C.A. Molecular genetics of human microcephaly. Curr. Opin. Neurol.14, 151–156 (2001). ArticleCAS Google Scholar
Jackson, A.P. et al. Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22–pter. Am. J. Hum. Genet.63, 541–546 (1998). ArticleCAS Google Scholar
Roberts, E. et al. The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1–13.2. Eur. J. Hum. Genet.7, 815–820 (1999). ArticleCAS Google Scholar
Moynihan, L. et al. A third novel locus for primary autosomal recessive microcephaly maps to chromosome 9q34. Am. J. Hum. Genet.66, 724–727 (2000). ArticleCAS Google Scholar
Jamieson, C.R., Govaerts, C. & Abramowicz, M.J. Primary autosomal recessive microcephaly: homozygosity mapping of MCPH4 to chromosome 15. Am. J. Hum. Genet.65, 1465–1469 (1999). ArticleCAS Google Scholar
Roberts, E. et al. Autosomal recessive primary microcephaly: an analysis of locus heterogeneity and phentoypic variation. J. Med. Genet. (in press) (2002).
Peltonen, L., Jalanko, A. & Varilo, T. Molecular genetics of the Finnish disease heritage. Hum. Mol. Genet.8, 1913–1923 (1999). ArticleCAS Google Scholar
den Hollander, A.I. et al. Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12). Nature Genet.23, 217–221 (1999). ArticleCAS Google Scholar
Saunders, R.D., Avides, M.C., Howard, T., Gonzalez, C. & Glover, D.M. The Drosophila gene abnormal spindle encodes a novel microtubule-associated protein that associates with the polar regions of the mitotic spindle. J. Cell Biol.137, 881–890 (1997). ArticleCAS Google Scholar
Craig, R. & Norbury, C. The novel murine calmodulin-binding protein Sha1 disrupts mitotic spindle and replication checkpoint functions in fission yeast. J. Cell Sci.11, 3609–3619 (1998). Google Scholar
Embryonic vertebrate central nervous system: revised terminology. The Boulder Committee. Anat. Rec.166, 257–262 (1970).
Anderson, S.A., Eisenstat, D.D., Shi, L. & Rubenstein, J.L. Interneuron migration from basal forebrain to neocortex: dependence on Dlx genes. Science278, 474–476 (1997). ArticleCAS Google Scholar
Wichterle, H., Garcia-Verdugo, J.M., Herrera, D.G. & Alvarez-Buylla, A. Young neurons from medial ganglionic eminence disperse in adult and embryonic brain. Nature Neurosci.2, 461–466 (1999). ArticleCAS Google Scholar
Seri, B., Garcia-Verdugo, J.M., McEwen, B.S. & Alvarez-Buylla, A. Astrocytes give rise to new neurons in the adult mammalian hippocampus. J. Neurosci.21, 7153–7160 (2001). ArticleCAS Google Scholar
Gould, E., Tanapat, P., Rydel, T. & Hastings, N. Regulation of hippocampal neurogenesis in adulthood. Biol. Psychiatry48, 715–720 (2000). ArticleCAS Google Scholar
Doetsch, F. & Alvarez-Buylla, A. Network of tangential pathways for neuronal migration in adult mammalian brain. Proc. Natl Acad. Sci. USA93, 14895–14900 (1996). ArticleCAS Google Scholar
do Carmo Avides, M., Tavares, A. & Glover, D.M. Polo kinase and Asp are needed to promote the mitotic organizing activity of centrosomes. Nature Cell Biol.3, 421–424 (2001). ArticleCAS Google Scholar
Wakefield, J.G., Bonaccorsi, S. & Gatti, M. The Drosophila protein asp is involved in microtubule organization during spindle formation and cytokinesis. J. Cell Biol.153, 637–648 (2001). ArticleCAS Google Scholar
Rakic, P. Neuronal migration and contact guidance in the primate telencephalon. Postgrad. Med. J.54, 25–40 (1978). PubMed Google Scholar
Takahashi, T., Nowakowski, R. and Caviness, V.S. Jr. The cell cycle of the pseudostratified ventricular epithelium of the murine cerebral wall. J. Neurosci.15, 6046–6057 (1995). ArticleCAS Google Scholar
Roegiers, F., Younger-Shepherd, S., Jan, L.Y. & Jan, Y.N. Two types of asymmetric divisions in the Drosophila sensory organ precursor cell lineage. Nature Cell Biol.3, 58–67 (2001). ArticleCAS Google Scholar
Lu, B., Jan, L. & Jan, Y.N. Control of cell divisions in the nervous system: symmetry and asymmetry. Annu. Rev. Neurosci.23, 531–556 (2000). ArticleCAS Google Scholar
Chenn, A. & McConnell, S.K. Cleavage orientation and the asymmetric inheritance of Notch1 immunoreactivity in mammalian neurogenesis. Cell82, 631–642 (1995). ArticleCAS Google Scholar
Bienz, M. Spindles cotton on to junctions, APC and EB1. Nature Cell Biol.3, E67–E69 (2001). ArticleCAS Google Scholar