Literature DB >> 16237707

Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2.

Kristen L Deak1, Margaret E Dickerson, Elwood Linney, David S Enterline, Timothy M George, Elizabeth C Melvin, Felicia L Graham, Deborah G Siegel, Preston Hammock, Lorraine Mehltretter, Alexander G Bassuk, John A Kessler, John R Gilbert, Marcy C Speer.   

Abstract

BACKGROUND: Vitamin A (retinol), in the form of retinoic acid (RA), is essential for normal development of the human embryo. Studies in the mouse and zebrafish have shown that retinol is metabolized in the developing spinal cord and must be maintained in a precise balance along the anteroposterior axis. Both excess and deficiency of RA can affect morphogenesis, including failures of neural tube closure.
METHODS: We chose to investigate 5 genes involved in the metabolism or synthesis of RA, ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2, for their role in the development of human neural tube defects, such as spina bifida.
RESULTS: An association analysis using both allelic and genotypic single-locus tests revealed a significant association between the risk for spina bifida and 3 polymorphisms in the gene ALDH1A2; however, we found no evidence of a significant multilocus association.
CONCLUSIONS: These results may suggest that polymorphisms in ALDH1A2 may influence the risk for lumbosacral myelomeningocele in humans.

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Year:  2005        PMID: 16237707     DOI: 10.1002/bdra.20183

Source DB:  PubMed          Journal:  Birth Defects Res A Clin Mol Teratol        ISSN: 1542-0752


  19 in total

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2.  Perturbation of Retinoid Homeostasis Increases Malformation Risk in Embryos Exposed to Pregestational Diabetes.

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Review 3.  Current perspectives on the genetic causes of neural tube defects.

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5.  Genetic contribution of retinoid-related genes to neural tube defects.

Authors:  Huili Li; Jing Zhang; Shuyuan Chen; Fang Wang; Ting Zhang; Lee Niswander
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Review 6.  Role of carotenoids and retinoids during heart development.

Authors:  Ioan Ovidiu Sirbu; Aimée Rodica Chiş; Alexander Radu Moise
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7.  Interaction of the SPG21 protein ACP33/maspardin with the aldehyde dehydrogenase ALDH16A1.

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Review 8.  Aldehyde dehydrogenases: from eye crystallins to metabolic disease and cancer stem cells.

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Review 9.  Genetics of human neural tube defects.

Authors:  Nicholas D E Greene; Philip Stanier; Andrew J Copp
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10.  ALDH1A2 (RALDH2) genetic variation in human congenital heart disease.

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Journal:  BMC Med Genet       Date:  2009-11-03       Impact factor: 2.103

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