Literature DB >> 15939212

Human neural tube defects: developmental biology, epidemiology, and genetics.

Eric R Detrait1, Timothy M George, Heather C Etchevers, John R Gilbert, Michel Vekemans, Marcy C Speer.   

Abstract

Birth defects (congenital anomalies) are the leading cause of death in babies under 1 year of age. Neural tube defects (NTD), with a birth incidence of approximately 1/1000 in American Caucasians, are the second most common type of birth defect after congenital heart defects. The most common presentations of NTD are spina bifida and anencephaly. The etiologies of NTDs are complex, with both genetic and environmental factors implicated. In this manuscript, we review the evidence for genetic etiology and for environmental influences, and we present current views on the developmental processes involved in human neural tube closure.

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Year:  2005        PMID: 15939212      PMCID: PMC2727639          DOI: 10.1016/j.ntt.2004.12.007

Source DB:  PubMed          Journal:  Neurotoxicol Teratol        ISSN: 0892-0362            Impact factor:   3.763


  87 in total

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Journal:  Genomics       Date:  1998-04-15       Impact factor: 5.736

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  118 in total

1.  Development of head organizer of the mouse embryo depends on a high level of mitochondrial metabolism.

Authors:  Xin Zhou; Kathryn V Anderson
Journal:  Dev Biol       Date:  2010-05-04       Impact factor: 3.582

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Authors:  G Wayne Brodland; Xiaoguang Chen; Paul Lee; Mungo Marsden
Journal:  HFSP J       Date:  2010-04-16

Review 3.  Development and differentiation of neural rosettes derived from human embryonic stem cells.

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Journal:  Stem Cell Rev       Date:  2006       Impact factor: 5.739

4.  An Inframe Trinucleotide Deletion in MTRR Exon 1 is Associated with the Risk of Spina Bifida.

Authors:  Jun Zhang; Xiao-Lu Dai; Gui-Cen Liu; Juan Wang; Xue-Yi Ren; Mu-Hua Jin; Nan-Nan Mi; Shu-Qin Wang
Journal:  Neuromolecular Med       Date:  2017-07-15       Impact factor: 3.843

5.  Exome analysis in an Estonian multiplex family with neural tube defects-a case report.

Authors:  Liina Pappa; Mart Kals; Paula Ann Kivistik; Andres Metspalu; Ann Paal; Tiit Nikopensius
Journal:  Childs Nerv Syst       Date:  2017-07-18       Impact factor: 1.475

Review 6.  The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects.

Authors:  Anne M Molloy; Lawrence C Brody; James L Mills; John M Scott; Peadar N Kirke
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2009-04

7.  Genetic variations in the GLUT3 gene associated with myelomeningocele.

Authors:  Brendan D Connealy; Hope Northrup; Kit Sing Au
Journal:  Am J Obstet Gynecol       Date:  2014-05-09       Impact factor: 8.661

8.  Essential role for fibrillin-2 in zebrafish notochord and vascular morphogenesis.

Authors:  John M Gansner; Erik C Madsen; Robert P Mecham; Jonathan D Gitlin
Journal:  Dev Dyn       Date:  2008-10       Impact factor: 3.780

9.  Sustained attention in children with two etiologies of early hydrocephalus.

Authors:  Maegan D Swartwout; Paul T Cirino; Amy W Hampson; Jack M Fletcher; Michael E Brandt; Maureen Dennis
Journal:  Neuropsychology       Date:  2008-11       Impact factor: 3.295

10.  Genetic association of the glycine cleavage system genes and myelomeningocele.

Authors:  Rita H Shah; Hope Northrup; James E Hixson; Alanna C Morrison; Kit Sing Au
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2016-09-13
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