Literature DB >> 9631651

Reeler: new tales on an old mutant mouse.

G D'Arcangelo1, T Curran.   

Abstract

Neurological mouse mutants provide an opportunity to dissect the complex mechanisms that underlie vertebrate brain development. Advances in genetic technologies have permitted the identification of genes disrupted in many mutants, allowing a molecular interpretation of the phenotypes. For several decades, the spontaneous mutant mouse reeler has been used as a model for the analysis of the development of laminated brain structures. In this ataxic mutant, the migration of many neurons is aberrant, resulting in disrupted cellular organization. Recently, reelin, the gene disrupted in the reeler mouse, has been identified, reelin encodes a novel extracellular molecule that controls neural cell positioning through mechanisms that are not yet completely understood. Analysis of the expression pattern and the properties of the reelin gene product (Reelin) suggests models for its function during brain development. Furthermore, the recent identification of genes that may function in the Reelin signaling pathway advances our knowledge of the molecular basis of neuronal migration.

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Year:  1998        PMID: 9631651     DOI: 10.1002/(SICI)1521-1878(199803)20:3<235::AID-BIES7>3.0.CO;2-Q

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  38 in total

1.  Sialidase-like Asp-boxes: sequence-similar structures within different protein folds.

Authors:  R R Copley; R B Russell; C P Ponting
Journal:  Protein Sci       Date:  2001-02       Impact factor: 6.725

Review 2.  Animal models of schizophrenia: a critical review.

Authors:  E R Marcotte; D M Pearson; L K Srivastava
Journal:  J Psychiatry Neurosci       Date:  2001-11       Impact factor: 6.186

3.  Dissection of the cellular and molecular events that position cerebellar Purkinje cells: a study of the math1 null-mutant mouse.

Authors:  Patricia Jensen; Huda Y Zoghbi; Dan Goldowitz
Journal:  J Neurosci       Date:  2002-09-15       Impact factor: 6.167

Review 4.  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

5.  Two distal downstream enhancers direct expression of the human apolipoprotein E gene to astrocytes in the brain.

Authors:  S Grehan; E Tse; J M Taylor
Journal:  J Neurosci       Date:  2001-02-01       Impact factor: 6.167

6.  The role of GABAergic system in neurodevelopmental disorders: a focus on autism and epilepsy.

Authors:  Paola Sgadò; Mark Dunleavy; Sacha Genovesi; Giovanni Provenzano; Yuri Bozzi
Journal:  Int J Physiol Pathophysiol Pharmacol       Date:  2011-09-09

7.  Neuroradiologic features of CASK mutations.

Authors:  J Takanashi; H Arai; S Nabatame; S Hirai; S Hayashi; J Inazawa; N Okamoto; A J Barkovich
Journal:  AJNR Am J Neuroradiol       Date:  2010-07-01       Impact factor: 3.825

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.  Replication of association between working memory and Reelin, a potential modifier gene in schizophrenia.

Authors:  Juho Wedenoja; Annamari Tuulio-Henriksson; Jaana Suvisaari; Anu Loukola; Tiina Paunio; Timo Partonen; Teppo Varilo; Jouko Lönnqvist; Leena Peltonen
Journal:  Biol Psychiatry       Date:  2009-11-17       Impact factor: 13.382

10.  Association analysis of two single-nucleotide polymorphisms of the RELN gene with autism in the South African population.

Authors:  Jyoti Rajan Sharma; Zainunisha Arieff; Hajirah Gameeldien; Muneera Davids; Mandeep Kaur; Lize van der Merwe
Journal:  Genet Test Mol Biomarkers       Date:  2012-12-05
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