Literature DB >> 19186242

Modeling neural tube defects in the mouse.

Irene E Zohn1, Anjali A Sarkar.   

Abstract

Neural tube defects (NTDs) are among the most common structural birth defects observed in humans. Mouse models provide an excellent experimental system to study the underlying causes of NTDs. These models not only allow for identification of the genes required for neurulation, they provide tractable systems for uncovering the developmental, pathological and molecular mechanisms underlying NTDs. In addition, mouse models are essential for elucidating the mechanisms of gene-environment and gene-gene interactions that contribute to the multifactorial inheritance of NTDs. In some cases these studies have led to development of approaches to prevent NTDs and provide an understanding of the underlying molecular mechanism of these therapies prevent NTDs.

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Year:  2008        PMID: 19186242     DOI: 10.1016/S0070-2153(08)00601-7

Source DB:  PubMed          Journal:  Curr Top Dev Biol        ISSN: 0070-2153            Impact factor:   4.897


  12 in total

1.  Generation and characterization of a novel neural crest marker allele, Inka1-LacZ, reveals a role for Inka1 in mouse neural tube closure.

Authors:  Bethany S Reid; Thomas D Sargent; Trevor Williams
Journal:  Dev Dyn       Date:  2010-04       Impact factor: 3.780

Review 2.  Membrane-anchored serine proteases in vertebrate cell and developmental biology.

Authors:  Roman Szabo; Thomas H Bugge
Journal:  Annu Rev Cell Dev Biol       Date:  2011-06-29       Impact factor: 13.827

3.  Craniorachischisis and omphalocele in a stillborn cynomolgus monkey (Macaca fascicularis).

Authors:  Charleen M Moore; Edward J Dick; Gene B Hubbard; Stephanie M Gardner; Betty G Dunn; Arthur R Brothman; Vick Williams; Suresh I Prajapati; Charles Keller; Michael D Davis
Journal:  Am J Med Genet A       Date:  2011-05-12       Impact factor: 2.802

4.  High levels of iron supplementation prevents neural tube defects in the Fpn1ffe mouse model.

Authors:  Bethany A Stokes; Julia A Sabatino; Irene E Zohn
Journal:  Birth Defects Res       Date:  2017-01-30       Impact factor: 2.344

5.  Prevention of neural tube defects in Lrp2 mutant mouse embryos by folic acid supplementation.

Authors:  Julia A Sabatino; Bethany A Stokes; Irene E Zohn
Journal:  Birth Defects Res       Date:  2017-01-20       Impact factor: 2.344

6.  The iron exporter ferroportin 1 is essential for development of the mouse embryo, forebrain patterning and neural tube closure.

Authors:  Jinzhe Mao; David M McKean; Sunita Warrier; Joshua G Corbin; Lee Niswander; Irene E Zohn
Journal:  Development       Date:  2010-08-11       Impact factor: 6.868

7.  Local protease signaling contributes to neural tube closure in the mouse embryo.

Authors:  Eric Camerer; Adrian Barker; Daniel N Duong; Rajkumar Ganesan; Hiroshi Kataoka; Ivo Cornelissen; Molly R Darragh; Arif Hussain; Yao-Wu Zheng; Yoga Srinivasan; Christopher Brown; Shan-Mei Xu; Jean B Regard; Chen-Yong Lin; Charles S Craik; Daniel Kirchhofer; Shaun R Coughlin
Journal:  Dev Cell       Date:  2010-01-19       Impact factor: 12.270

8.  Histology Atlas of the Developing Prenatal and Postnatal Mouse Central Nervous System, with Emphasis on Prenatal Days E7.5 to E18.5.

Authors:  Vivian S Chen; James P Morrison; Myra F Southwell; Julie F Foley; Brad Bolon; Susan A Elmore
Journal:  Toxicol Pathol       Date:  2017-09-11       Impact factor: 1.902

Review 9.  Does the cranial mesenchyme contribute to neural fold elevation during neurulation?

Authors:  Irene E Zohn; Anjali A Sarkar
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2012-09-03

10.  Hectd1 regulates intracellular localization and secretion of Hsp90 to control cellular behavior of the cranial mesenchyme.

Authors:  Anjali A Sarkar; Irene E Zohn
Journal:  J Cell Biol       Date:  2012-03-19       Impact factor: 10.539

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