Genetics of human neural tube defects

An association study of 45 folate-related genes in spina bifida: Involvement ofcubilin(CUBN) andtRNA aspartic acid methyltransferase 1(TRDMT1)

(2009) Barbara Franke et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Understanding the causes and prevention of neural tube defects: Insights from thesplotchmouse model

(2009) Nicholas D.E. Greene et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Interaction ofPDGFRApromoter haplotypes and maternal environmental exposures in the risk of spina bifida

(2009) Mascha Toepoel et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Uncoupling protein 2 polymorphisms as risk factors for NTDs

(2009) Adam Mitchell et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Insights into metabolic mechanisms underlying folate-responsive neural tube defects: A minireview

(2009) Anna E. Beaudin et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

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

(2009) Anne M. Molloy et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects

(2009) Gary M Shaw et al.   BMC Medical Genetics

Regulation of Planar Cell Polarity by Smurf Ubiquitin Ligases

(2009) Masahiro Narimatsu et al.   CELL

Non-canonical Wnt signaling regulates cell polarity in female reproductive tract development via van gogh-like 2

(2009) A. L. vandenBerg et al.   DEVELOPMENT

Genetic or nutritional disorders in homocysteine or folate metabolism increase protein N-homocysteinylation in mice

(2009) Hieronim Jakubowski et al.   FASEB JOURNAL

Analysis of the MTHFD1 promoter and risk of neural tube defects

(2009) Nicola Carroll et al.   HUMAN GENETICS

Copy number variants, diseases and gene expression

(2009) C. N. Henrichsen et al.   HUMAN MOLECULAR GENETICS

Novel mutations inVANGL1in neural tube defects

(2009) Zoha Kibar et al.   HUMAN MUTATION

Development of the vertebrate central nervous system: formation of the neural tube

(2009) Nicholas D. E. Greene et al.   PRENATAL DIAGNOSIS

Neural tube defects in mice with reduced levels of inositol 1,3,4-trisphosphate 5/6-kinase

(2009) M. P. Wilson et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Grainyhead genes and mammalian neural tube closure

(2008) Peter Gustavsson et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

NicotinamideN-methyl transferase (NNMT) gene polymorphisms and risk for spina bifida

(2008) Wei Lu et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Refinement of 2q and 7p loci in a large multiplex NTD family

(2008) Demetra S. Stamm et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Microarray analysis of E9.5 reduced folate carrier (RFC1; Slc19a1) knockout embryos reveals altered expression of genes in the cubilin-megalin multiligand endocytic receptor complex

(2008) Janee Gelineau-van Waes et al.   BMC GENOMICS

The planar polarity pathway

(2008) David Strutt   CURRENT BIOLOGY

Nutrient Pathways and Neural Tube Defects

(2008) Suzan L. Carmichael et al.   EPIDEMIOLOGY

Gene-environment interactions in the causation of neural tube defects: folate deficiency increases susceptibility conferred by loss of Pax3 function

(2008) K. A. Burren et al.   HUMAN MOLECULAR GENETICS

The MTHFD1 p.Arg653Gln variant alters enzyme function and increases risk for congenital heart defects

(2008) Karen E. Christensen et al.   HUMAN MUTATION

Genetic interaction between members of the Vangl family causes neural tube defects in mice

(2008) E. Torban et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Genes in Glucose Metabolism and Association With Spina Bifida

(2008) Christina M. Davidson et al.   Reproductive Sciences

Murine Dishevelled 3 Functions in Redundant Pathways with Dishevelled 1 and 2 in Normal Cardiac Outflow Tract, Cochlea, and Neural Tube Development

(2008) S. Leah Etheridge et al.   PLoS Genetics

Correlation of polymorphism ofMTHFRs andRFC-1 genes with neural tube defects in China

(2007) Yali Shang et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY