(Q35500353)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21254360%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

title

NAT1, NOS3, and TYMS genotypes and the risk of conotruncal cardiac defects (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21254360%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1

1 reference

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20 January 2020

3

Elizabeth Goldmuntz

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21254360%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

author name string

Laura E Mitchell

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21254360%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

publication date

1 December 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21254360%20AND%20SRC:MED&resulttype=core&format=json

Birth Defects Research Part A: Clinical and Molecular Teratology

20 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21254360%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

volume

91

1 reference

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20 January 2020

issue

1

1 reference

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20 January 2020

page(s)

61-65

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21254360%20AND%20SRC:MED&resulttype=core&format=json

Gene-gene interactions in the folate metabolic pathway and the risk of conotruncal heart defects

20 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4404296

Variants of folate metabolism genes and the risk of conotruncal cardiac defects.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4404296

Variants of folate metabolism genes and risk of left-sided cardiac defects

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4404296

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4404296

Noninherited risk factors and congenital cardiovascular defects: current knowledge: a scientific statement from the American Heart Association Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4404296

A 6 bp polymorphism in the thymidylate synthase gene causes message instability and is associated with decreased intratumoral TS mRNA levels

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4404296

Thymidylate synthase as a translational regulator of cellular gene expression

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4404296

Allowing for missing parents in genetic studies of case-parent triads

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4404296

A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4404296

Homocysteine induces congenital defects of the heart and neural tube: effect of folic acid

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4404296

Acetylation of p-aminobenzoylglutamate, a folic acid catabolite, by recombinant human arylamine N-acetyltransferase and U937 cells

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4404296

Evidence that the risk of spina bifida is influenced by genetic variation at the NOS3 locus

12 July 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.20745

Genetic evidence that nitric oxide modulates homocysteine: the NOS3 894TT genotype is a risk factor for hyperhomocystenemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.20745

Congenital heart defects and genetic variants in the methylenetetrahydroflate reductase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.20745

A common insertion/deletion polymorphism of the thymidylate synthase (TYMS) gene is a determinant of red blood cell folate and homocysteine concentrations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.20745

Method for using complete and incomplete trios to identify genes related to a quantitative trait.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.20745

Periconceptional multivitamin intake during early pregnancy, genetic variation of acetyl-N-transferase 1 (NAT1), and risk for orofacial clefts

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.20745

Genetic variation of infant reduced folate carrier (A80G) and risk of orofacial defects and congenital heart defects in China

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.20745

Immunochemical detection of arylamine N-acetyltransferase during mouse embryonic development and in adult mouse brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.20745

Thymidylate synthase: a novel genetic determinant of plasma homocysteine and folate levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.20745

Common 894G>T single nucleotide polymorphism in the gene coding for endothelial nitric oxide synthase (eNOS) and risk of congenital heart defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.20745

Associations between polymorphisms within the thymidylate synthase gene and spina bifida

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.20745

Thymidylate synthase promoter polymorphism, interaction with folate intake, and risk of colorectal adenomas.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4404296

Genotype dependent and cigarette specific effects on endothelial nitric oxide synthase gene expression and enzyme activity

26 September 2018

1 reference

12 December 2020

Seeking causes: Classifying and evaluating congenital heart defects in etiologic studies

1 reference

12 December 2020

Chromosome 22q11 deletion in patients with ventricular septal defect: frequency and associated cardiovascular anomalies

1 reference

12 December 2020

Loss of function polymorphisms in NAT1 protect against spina bifida

1 reference

12 December 2020

Association of chromosome 22q11 deletion with isolated anomalies of aortic arch laterality and branching

1 reference

12 December 2020

Risks of human conotruncal heart defects associated with 32 single nucleotide polymorphisms of selected cardiovascular disease-related genes

1 reference

12 December 2020

Identifiers

DOI

10.1002/BDRA.20745

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21254360%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21254360%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

PubMed publication ID

21254360

1 reference