Literature DB >> 12717817

Teratogenic alleles and neurodevelopmental disorders.

William G Johnson1.   

Abstract

The genetic interaction between mother and fetus during pregnancy is discussed, focusing on teratogenic alleles that act in the mother to alter fetal development and contribute to a neurodevelopmental disorder. For these alleles, the mother is the genetic patient. Teratogenic alleles interact with modifying and specificity alleles that act in the fetus and with environmental factors. Based on examples of the model, two candidate mechanisms emerge as contributors to neurodevelopmental disorders, folate-homocysteine pathways and immune/inflammatory mechanisms. Both, acting in mothers, affect fetal development and contain many polymorphic genes. These two systems interact with each other. Common functional polymorphisms of mild effect in these two systems of interacting genes are good candidates for teratogenic alleles. The presence of teratogenic alleles complicates gene identification for neurodevelopmental disorders. However, using the special methods required to identify teratogenic alleles is important because this could lead to new approaches to prevention and improved therapy of these disorders. Copyright 2003 Wiley Periodicals, Inc.

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Year:  2003        PMID: 12717817     DOI: 10.1002/bies.10268

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


  6 in total

1.  A functional polymorphism in the reduced folate carrier gene and DNA hypomethylation in mothers of children with autism.

Authors:  S Jill James; Stepan Melnyk; Stefanie Jernigan; Oleksandra Pavliv; Timothy Trusty; Sara Lehman; Lisa Seidel; David W Gaylor; Mario A Cleves
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2010-09       Impact factor: 3.568

2.  Investigation of maternal genotype effects in autism by genome-wide association.

Authors:  Han Yuan; Joseph D Dougherty
Journal:  Autism Res       Date:  2014-02-25       Impact factor: 5.216

3.  Maternal genetic mutations as gestational and early life influences in producing psychiatric disease-like phenotypes in mice.

Authors:  Georgia Gleason; Bojana Zupan; Miklos Toth
Journal:  Front Psychiatry       Date:  2011-05-11       Impact factor: 4.157

4.  The emergence of human-evolutionary medical genomics.

Authors:  Bernard J Crespi
Journal:  Evol Appl       Date:  2010-10-12       Impact factor: 5.183

5.  Impact of MTHFR (C677T) gene polymorphism on antiepileptic drug monotherapy in North Indian epileptic population.

Authors:  Murali Munisamy; Mubarak Al-Gahtany; Manjari Tripathi; Vivekanandhan Subbiah
Journal:  Ann Saudi Med       Date:  2015 Jan-Feb       Impact factor: 1.526

Review 6.  Methylenetetrahydrofolate reductase and transcobalamin genetic polymorphisms in human spontaneous abortion: biological and clinical implications.

Authors:  Henrik Zetterberg
Journal:  Reprod Biol Endocrinol       Date:  2004-02-17       Impact factor: 5.211

  6 in total

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