Literature DB >> 21288712

What disorders of cortical development tell us about the cortex: one plus one does not always make two.

M Chiara Manzini1, Christopher A Walsh.   

Abstract

The unique size and complexity of the human cerebral cortex are achieved via a long and precisely regulated developmental process controlling neurogenesis, neuronal migration and differentiation. Traditionally, disorders of cortical development have been classified on the basis of the most obvious defects in one of these developmental steps. However, the more we learn about the cellular biological roles of genes that are essential for cortical development, the more we realize that these functions map onto molecular processes, but not so cleanly onto anatomical processes. Essential genes might be involved in both proliferation and migration as well as differentiation, reflecting roles for underlying molecular mechanisms in different phases of development and causing a stunning variety of cortical defects.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21288712      PMCID: PMC3139684          DOI: 10.1016/j.gde.2011.01.006

Source DB:  PubMed          Journal:  Curr Opin Genet Dev        ISSN: 0959-437X            Impact factor:   5.578


  54 in total

1.  Cdk5rap2 interacts with pericentrin to maintain the neural progenitor pool in the developing neocortex.

Authors:  Joshua J Buchman; Huan-Chung Tseng; Ying Zhou; Christopher L Frank; Zhigang Xie; Li-Huei Tsai
Journal:  Neuron       Date:  2010-05-13       Impact factor: 17.173

Review 2.  Genetics of the polymicrogyria syndromes.

Authors:  A Jansen; E Andermann
Journal:  J Med Genet       Date:  2005-05       Impact factor: 6.318

3.  Primary cellular meningeal defects cause neocortical dysplasia and dyslamination.

Authors:  Jonathan H Hecht; Julie A Siegenthaler; Katelin P Patterson; Samuel J Pleasure
Journal:  Ann Neurol       Date:  2010-10       Impact factor: 10.422

4.  GPR56 regulates pial basement membrane integrity and cortical lamination.

Authors:  Shihong Li; Zhaohui Jin; Samir Koirala; Lihong Bu; Lei Xu; Richard O Hynes; Christopher A Walsh; Gabriel Corfas; Xianhua Piao
Journal:  J Neurosci       Date:  2008-05-28       Impact factor: 6.167

5.  Ndel1 operates in a common pathway with LIS1 and cytoplasmic dynein to regulate cortical neuronal positioning.

Authors:  Tianzhi Shu; Ramses Ayala; Minh-Dang Nguyen; Zhigang Xie; Joseph G Gleeson; Li-Huei Tsai
Journal:  Neuron       Date:  2004-10-14       Impact factor: 17.173

6.  Mitotic spindle regulation by Nde1 controls cerebral cortical size.

Authors:  Yuanyi Feng; Christopher A Walsh
Journal:  Neuron       Date:  2004-10-14       Impact factor: 17.173

7.  Mutations in the FKRP gene can cause muscle-eye-brain disease and Walker-Warburg syndrome.

Authors:  D Beltran-Valero de Bernabé; T Voit; C Longman; A Steinbrecher; V Straub; Y Yuva; R Herrmann; J Sperner; C Korenke; C Diesen; W B Dobyns; H G Brunner; H van Bokhoven; M Brockington; F Muntoni
Journal:  J Med Genet       Date:  2004-05       Impact factor: 6.318

8.  Dual subcellular roles for LIS1 and dynein in radial neuronal migration in live brain tissue.

Authors:  Jin-Wu Tsai; K Helen Bremner; Richard B Vallee
Journal:  Nat Neurosci       Date:  2007-07-08       Impact factor: 24.884

9.  Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance.

Authors:  Max A Tischfield; Hagit N Baris; Chen Wu; Guenther Rudolph; Lionel Van Maldergem; Wei He; Wai-Man Chan; Caroline Andrews; Joseph L Demer; Richard L Robertson; David A Mackey; Jonathan B Ruddle; Thomas D Bird; Irene Gottlob; Christina Pieh; Elias I Traboulsi; Scott L Pomeroy; David G Hunter; Janet S Soul; Anna Newlin; Louise J Sabol; Edward J Doherty; Clara E de Uzcátegui; Nicolas de Uzcátegui; Mary Louise Z Collins; Emin C Sener; Bettina Wabbels; Heide Hellebrand; Thomas Meitinger; Teresa de Berardinis; Adriano Magli; Costantino Schiavi; Marco Pastore-Trossello; Feray Koc; Agnes M Wong; Alex V Levin; Michael T Geraghty; Maria Descartes; Maree Flaherty; Robyn V Jamieson; H U Møller; Ingo Meuthen; David F Callen; Janet Kerwin; Susan Lindsay; Alfons Meindl; Mohan L Gupta; David Pellman; Elizabeth C Engle
Journal:  Cell       Date:  2010-01-08       Impact factor: 41.582

Review 10.  Genetics and biology of microcephaly and lissencephaly.

Authors:  Ganeshwaran H Mochida
Journal:  Semin Pediatr Neurol       Date:  2009-09       Impact factor: 1.636

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  70 in total

Review 1.  Transcriptional co-regulation of neuronal migration and laminar identity in the neocortex.

Authors:  Kenneth Y Kwan; Nenad Sestan; E S Anton
Journal:  Development       Date:  2012-05       Impact factor: 6.868

Review 2.  The choroid plexus and cerebrospinal fluid: emerging roles in development, disease, and therapy.

Authors:  Maria K Lehtinen; Christopher S Bjornsson; Susan M Dymecki; Richard J Gilbertson; David M Holtzman; Edwin S Monuki
Journal:  J Neurosci       Date:  2013-11-06       Impact factor: 6.167

3.  Rescue of CAMDI deletion-induced delayed radial migration and psychiatric behaviors by HDAC6 inhibitor.

Authors:  Toshifumi Fukuda; Shun Nagashima; Takaya Abe; Hiroshi Kiyonari; Ryoko Inatome; Shigeru Yanagi
Journal:  EMBO Rep       Date:  2016-10-13       Impact factor: 8.807

4.  In vivo clonal overexpression of neuroligin 3 and neuroligin 2 in neurons of the rat cerebral cortex: Differential effects on GABAergic synapses and neuronal migration.

Authors:  Christopher D Fekete; Tzu-Ting Chiou; Celia P Miralles; Rachel S Harris; Christopher G Fiondella; Joseph J Loturco; Angel L De Blas
Journal:  J Comp Neurol       Date:  2015-04-08       Impact factor: 3.215

Review 5.  Molecular control of neurogenesis: a view from the mammalian cerebral cortex.

Authors:  Ben Martynoga; Daniela Drechsel; François Guillemot
Journal:  Cold Spring Harb Perspect Biol       Date:  2012-10-01       Impact factor: 10.005

6.  Ex utero electroporation and whole hemisphere explants: a simple experimental method for studies of early cortical development.

Authors:  Anna J Nichols; Ryan S O'Dell; Teresa A Powrozek; Eric C Olson
Journal:  J Vis Exp       Date:  2013-04-03       Impact factor: 1.355

Review 7.  Genetic causes of microcephaly and lessons for neuronal development.

Authors:  Edward C Gilmore; Christopher A Walsh
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2012-10-04       Impact factor: 5.814

Review 8.  Transcriptional dysregulation of neocortical circuit assembly in ASD.

Authors:  Kenneth Y Kwan
Journal:  Int Rev Neurobiol       Date:  2013       Impact factor: 3.230

9.  Arl13b in primary cilia regulates the migration and placement of interneurons in the developing cerebral cortex.

Authors:  Holden Higginbotham; Tae-Yeon Eom; Laura E Mariani; Amelia Bachleda; Joshua Hirt; Vladimir Gukassyan; Corey L Cusack; Cary Lai; Tamara Caspary; E S Anton
Journal:  Dev Cell       Date:  2012-11-13       Impact factor: 12.270

10.  Radial and tangential neuronal migration pathways in the human fetal brain: anatomically distinct patterns of diffusion MRI coherence.

Authors:  James Kolasinski; Emi Takahashi; Allison A Stevens; Thomas Benner; Bruce Fischl; Lilla Zöllei; P Ellen Grant
Journal:  Neuroimage       Date:  2013-05-11       Impact factor: 6.556

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