(Q44409883)

2 December 2017

title

Association between 5,10-methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and conotruncal heart defects (English)

1 reference

2 December 2017

Association between 5,10-Methylenetetrahydrofolate Reductase C677T and A1298C Polymorphisms and Conotruncal Heart Defects (English)

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.043

26 December 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12705333

26 December 2023

2

Simona Vittorini

1 reference

2 December 2017

1

Simona Storti

1 reference

2 December 2017

9

Aldo Clerico

1 reference

2 December 2017

8

Andrea Biagini

1 reference

2 December 2017

6

Andrea Ripoli

1 reference

2 December 2017

4

Monica Sacchelli

1 reference

2 December 2017

3

Maria R. Iascone

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12705333

26 December 2023

author name string

Anita Collavoli

5

1 reference

2 December 2017

Guido Cocchi

7

1 reference

2 December 2017

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12705333

26 December 2023

publication date

1 March 2003

1 reference

Clinical Chemistry and Laboratory Medicine

2 December 2017

published in

1 reference

2 December 2017

volume

41

1 reference

2 December 2017

issue

3

1 reference

2 December 2017

page(s)

276-280

1 reference

Role of cardiac neural crest cells in cardiovascular development

2 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.043

Neural crest is involved in development of abnormal myocardial function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.043

Maternal periconceptional vitamin use, genetic variation of infant reduced folate carrier (A80G), and risk of spina bifida

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.043

Maternal hyperhomocysteinemia: a risk factor for neural-tube defects?

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.043

Congenital heart defects and maternal derangement of homocysteine metabolism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.043

Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR)

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.043

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.043

A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.043

5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.043

Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.043

Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.043

C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.043

Infant methylenetetrahydrofolate reductase 677TT genotype is a risk factor for congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.043

Association of the C677T methylenetetrahydrofolate reductase mutation and elevated homocysteine levels with congenital cardiac malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.043

Methylenetetrahydrofolate reductase polymorphism and pre-eclampsia

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.043

Purification of genomic DNA from human whole blood by isopropanol-fractionation with concentrated Nal and SDS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.043

Polymorphisms in the methylenetetrahydrofolate reductase gene are associated with susceptibility to acute leukemia in adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.043

Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.043

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.043

Reduction of urinary tract and cardiovascular defects by periconceptional multivitamin supplementation

21 January 2018

4

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.043

Screening of the C677T mutation on the methylenetetrahydrofolate reductase gene in French patients with neural tube defects

26 December 2023

13

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.043

Linkage disequilibrium of MTHFR genotypes 677C/T-1298A/C in the German population and association studies in probands with neural tube defects(NTD)

26 December 2023

15

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.043

5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review

26 December 2023

24

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.043

Genetic selection and folate intake during pregnancy

26 December 2023

26

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.043

26 December 2023

Identifiers

1 reference

2 December 2017

1 reference