Literature DB >> 11553932

Neuronal migration disorders.

J G Gleeson1.   

Abstract

Neuronal migration disorders are a category of developmental brain disorders leading to cortical dysplasia. This group of disorders is characterized by defective movement of neurons from the place of origin along the lining of the lateral ventricle, to the eventual place of residence in the correct laminar position within the cerebral cortex. As a result of defective migration, affected individuals typically display mental retardation and epilepsy. Although patients with the more severe forms of these disorders often present during infancy, patients may present at any age from newborn to adulthood. The migration defect may be generalized or focal, and may be disturbed at any of several stages, leading to several distinct radiographical and clinical presentations. The human phenotypes suggests that there are at least four distinct and clinically-important steps in cortical neuronal migration, and the identification of the responsible genes suggests that multiple cellular processes are critical for correct neuronal positioning. Copyright 2001 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2001        PMID: 11553932     DOI: 10.1002/mrdd.1024

Source DB:  PubMed          Journal:  Ment Retard Dev Disabil Res Rev        ISSN: 1080-4013


  12 in total

1.  Leading tip drives soma translocation via forward F-actin flow during neuronal migration.

Authors:  Min He; Zheng-hong Zhang; Chen-bing Guan; Di Xia; Xiao-bing Yuan
Journal:  J Neurosci       Date:  2010-08-11       Impact factor: 6.167

2.  Activation of extracellular regulated kinase and mechanistic target of rapamycin pathway in focal cortical dysplasia.

Authors:  Vinit V Patil; Miguel Guzman; Angela N Carter; Geetanjali Rathore; Daniel Yoshor; Daniel Curry; Angus Wilfong; Satish Agadi; John W Swann; Adekunle M Adesina; Meenakshi B Bhattacharjee; Anne E Anderson
Journal:  Neuropathology       Date:  2015-09-18       Impact factor: 1.906

3.  T-Box transcription factor Tbx20 regulates a genetic program for cranial motor neuron cell body migration.

Authors:  Mi-Ryoung Song; Ryuichi Shirasaki; Chen-Leng Cai; Esmeralda C Ruiz; Sylvia M Evans; Soo-Kyung Lee; Samuel L Pfaff
Journal:  Development       Date:  2006-12       Impact factor: 6.868

4.  Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1.

Authors:  Steven W Threlkeld; Melissa M McClure; Jilin Bai; Yu Wang; Joe J LoTurco; Glenn D Rosen; R Holly Fitch
Journal:  Brain Res Bull       Date:  2006-12-05       Impact factor: 4.077

Review 5.  Cadherins as regulators of neuronal polarity.

Authors:  Annette Gärtner; Eugenio F Fornasiero; Carlos G Dotti
Journal:  Cell Adh Migr       Date:  2014-11-14       Impact factor: 3.405

6.  An isoform-specific SnoN1-FOXO1 repressor complex controls neuronal morphogenesis and positioning in the mammalian brain.

Authors:  Mai Anh Huynh; Yoshiho Ikeuchi; Stuart Netherton; Luis de la Torre-Ubieta; Rahul Kanadia; Judith Stegmüller; Constance Cepko; Shirin Bonni; Azad Bonni
Journal:  Neuron       Date:  2011-03-10       Impact factor: 17.173

Review 7.  Genetic regulation of human brain development: lessons from Mendelian diseases.

Authors:  Tracy J Dixon-Salazar; Joseph G Gleeson
Journal:  Ann N Y Acad Sci       Date:  2010-11-09       Impact factor: 5.691

8.  The in vivo roles of STEF/Tiam1, Rac1 and JNK in cortical neuronal migration.

Authors:  Takeshi Kawauchi; Kaori Chihama; Yo-ichi Nabeshima; Mikio Hoshino
Journal:  EMBO J       Date:  2003-08-15       Impact factor: 11.598

9.  Placenta defects and embryonic lethality resulting from disruption of mouse hydroxysteroid (17-beta) dehydrogenase 2 gene.

Authors:  Pia Rantakari; Leena Strauss; Riku Kiviranta; Heidi Lagerbohm; Jenni Paviala; Irma Holopainen; Seppo Vainio; Pirjo Pakarinen; Matti Poutanen
Journal:  Mol Endocrinol       Date:  2007-11-29

10.  DNA repair modulates the vulnerability of the developing brain to alkylating agents.

Authors:  G E Kisby; A Olivas; T Park; M Churchwell; D Doerge; L D Samson; S L Gerson; M S Turker
Journal:  DNA Repair (Amst)       Date:  2009-01-21
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