Literature DB >> 10906798

Neuronal migration disorders: from genetic diseases to developmental mechanisms.

J G Gleeson1, C A Walsh.   

Abstract

Neurons that constitute the cerebral cortex must migrate hundreds of cell-body distances from their place of birth, and through several anatomical boundaries, to reach their final position within the correct cortical layer. Human neurological conditions associated with abnormal neuronal migration, together with spontaneous and engineered mouse mutants, define at least four distinct steps in cortical neuronal migration. Many of the genes that control neuronal migration have strong genetic or biochemical links to the cytoskeleton, suggesting that the field of neuronal migration might be closing in on the underlying cytoskeletal events.

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Year:  2000        PMID: 10906798     DOI: 10.1016/s0166-2236(00)01607-6

Source DB:  PubMed          Journal:  Trends Neurosci        ISSN: 0166-2236            Impact factor:   13.837


  92 in total

Review 1.  Action of thyroid hormone in brain.

Authors:  J Bernal
Journal:  J Endocrinol Invest       Date:  2002-03       Impact factor: 4.256

Review 2.  Congenital abnormalities of the central nervous system.

Authors:  Christopher Verity; Helen Firth; Charles ffrench-Constant
Journal:  J Neurol Neurosurg Psychiatry       Date:  2003-03       Impact factor: 10.154

Review 3.  Application of in utero electroporation and live imaging in the analyses of neuronal migration during mouse brain development.

Authors:  Yoshiaki V Nishimura; Tomoyasu Shinoda; Yutaka Inaguma; Hidenori Ito; Koh-Ichi Nagata
Journal:  Med Mol Morphol       Date:  2012-03-20       Impact factor: 2.309

4.  N-cadherin regulates radial glial fiber-dependent migration of cortical locomoting neurons.

Authors:  Mima Shikanai; Kazunori Nakajima; Takeshi Kawauchi
Journal:  Commun Integr Biol       Date:  2011-05

Review 5.  Strategies for analyzing neuronal progenitor development and neuronal migration in the developing cerebral cortex.

Authors:  Holden Higginbotham; Yukako Yokota; E S Anton
Journal:  Cereb Cortex       Date:  2010-11-15       Impact factor: 5.357

6.  Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans.

Authors:  Thomas Gstrein; Andrew Edwards; Anna Přistoupilová; Ines Leca; Martin Breuss; Sandra Pilat-Carotta; Andi H Hansen; Ratna Tripathy; Anna K Traunbauer; Tobias Hochstoeger; Gavril Rosoklija; Marco Repic; Lukas Landler; Viktor Stránecký; Gerhard Dürnberger; Thomas M Keane; Johannes Zuber; David J Adams; Jonathan Flint; Tomas Honzik; Marta Gut; Sergi Beltran; Karl Mechtler; Elliott Sherr; Stanislav Kmoch; Ivo Gut; David A Keays
Journal:  Nat Neurosci       Date:  2018-01-08       Impact factor: 24.884

7.  Gap junctions/hemichannels modulate interkinetic nuclear migration in the forebrain precursors.

Authors:  Xiuxin Liu; Kazue Hashimoto-Torii; Masaaki Torii; Chen Ding; Pasko Rakic
Journal:  J Neurosci       Date:  2010-03-24       Impact factor: 6.167

8.  Contributions of cortical subventricular zone to the development of the human cerebral cortex.

Authors:  Nada Zecevic; Yanhui Chen; Radmila Filipovic
Journal:  J Comp Neurol       Date:  2005-10-17       Impact factor: 3.215

9.  Rest represses maturation within migrating facial branchiomotor neurons.

Authors:  Crystal E Love; Victoria E Prince
Journal:  Dev Biol       Date:  2015-03-11       Impact factor: 3.582

10.  Cortical dysplasia resembling human type 2 lissencephaly in mice lacking all three APP family members.

Authors:  Jochen Herms; Brigitte Anliker; Sabine Heber; Sabine Ring; Martin Fuhrmann; Hans Kretzschmar; Sangram Sisodia; Ulrike Müller
Journal:  EMBO J       Date:  2004-09-23       Impact factor: 11.598

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