Maternal MTHFR interacts with the offspring's BCL3 genotypes, but not with TGFA, in increasing risk to nonsyndromic cleft lip with or without cleft palate (Q44822426)

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scientific article published in July 2004

Language	Label	Description	Also known as
English	Maternal MTHFR interacts with the offspring's BCL3 genotypes, but not with TGFA, in increasing risk to nonsyndromic cleft lip with or without cleft palate	scientific article published in July 2004

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Maternal MTHFR interacts with the offspring's BCL3 genotypes, but not with TGFA, in increasing risk to nonsyndromic cleft lip with or without cleft palate (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

1 reference

based on heuristic

inferred from title

Maria Rita Passos-Bueno

7

object named as

Maria Rita Passos-Bueno

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Europe PubMed Central

PubMed publication ID

6 December 2017

Sergio Russo Matioli

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object named as

Sergio R Matioli

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Europe PubMed Central

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6 December 2017

author name string

Dinamar A Gaspar

1

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Europe PubMed Central

PubMed publication ID

6 December 2017

Rita de Cássia Pavanello

3

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Belmino C Araújo

4

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Nivaldo Alonso

5

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Diego Wyszynski

6

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Europe PubMed Central

PubMed publication ID

6 December 2017

publication date

1 July 2004

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Europe PubMed Central

PubMed publication ID

6 December 2017

European Journal of Human Genetics

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Europe PubMed Central

PubMed publication ID

6 December 2017

12

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6 December 2017

7

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Europe PubMed Central

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6 December 2017

521-526

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PubMed publication ID

6 December 2017

Genetics of nonsyndromic oral clefts revisited

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

21 January 2018

Gene/environment causes of cleft lip and/or palate

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

21 January 2018

Risks of orofacial clefts in children born to women using multivitamins containing folic acid periconceptionally

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

21 January 2018

Infant C677T mutation in MTHFR, maternal periconceptional vitamin use, and cleft lip.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

21 January 2018

Linkage analysis of three candidate regions of chromosome 1 in nonsyndromic familial orofacial cleft

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

21 January 2018

Maternal MTHFR genotype contributes to the risk of non-syndromic cleft lip and palate

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

21 January 2018

Exploring the effects of methylenetetrahydrofolate reductase gene variants C677T and A1298C on the risk of orofacial clefts in 261 Norwegian case-parent triads

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

21 January 2018

Does the interaction between maternal folate intake and the methylenetetrahydrofolate reductase polymorphisms affect the risk of cleft lip with or without cleft palate?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

21 January 2018

Subgroup studies of black admixture within a mixed population of Bahia, Brazil

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

21 January 2018

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

21 January 2018

Performing the exact test of Hardy-Weinberg proportion for multiple alleles

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

21 January 2018

Testing for linkage disequilibrium in genotypic data using the Expectation-Maximization algorithm

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

21 January 2018

Maternal 677CT/1298AC genotype of the MTHFR gene as a risk factor for cleft lip

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

21 January 2018

The candidate proto-oncogene bcl-3 encodes a transcriptional coactivator that activates through NF-kappa B p50 homodimers

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

21 January 2018

Homocysteine oxidation and apoptosis: a potential cause of cleft palate

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

21 January 2018

Case-Only Design to Measure Gene-Gene Interaction

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

21 January 2018

Population-based case control study of folic acid supplementation during pregnancy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

7 January 2021

based on heuristic

inferred from DOI database lookup

Role of the C677T polymorphism at the MTHFR gene on risk to nonsyndromic cleft lip with/without cleft palate: results from a case-control study in Brazil

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

7 January 2021

based on heuristic

inferred from DOI database lookup

Evidence that BCL3 plays a role in the etiology of nonsyndromic oral clefts in Brazilian families

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

7 January 2021

based on heuristic

inferred from DOI database lookup

Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in Brazilian patients: results of a large case-control study

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

7 January 2021

based on heuristic

inferred from DOI database lookup

Multiplex PCR amplification from the CFTR gene using DNA prepared from buccal brushes/swabs

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

7 January 2021

based on heuristic

inferred from DOI database lookup

Prevalence of the mutation C677 --> T in the methylene tetrahydrofolate reductase gene among distinct ethnic groups in Brazil

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

7 January 2021

based on heuristic

inferred from DOI database lookup

Methylenetetrahydrofolate reductase (MTHFR): incidence of mutations C677T and A1298C in Brazilian population and its correlation with plasma homocysteine levels in spina bifida

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

7 January 2021

based on heuristic

inferred from DOI database lookup

Decreased proportion of female newborn infants homozygous for the 677 C-->T mutation in methylenetetrahydrofolate reductase

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

7 January 2021

based on heuristic

inferred from DOI database lookup

Testing candidate genes for non-syndromic oral clefts using a case-parent trio design

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

7 January 2021

based on heuristic

inferred from DOI database lookup

The oncoprotein Bcl-3 can facilitate NF-kappa B-mediated transactivation by removing inhibiting p50 homodimers from select kappa B sites.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

7 January 2021

based on heuristic

inferred from DOI database lookup

Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex families

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

7 January 2021

based on heuristic

inferred from DOI database lookup

Suggestive linkage between markers on chromosome 19q13.2 and nonsyndromic orofacial cleft malformation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

7 January 2021

based on heuristic

inferred from DOI database lookup

Nonsyndromic orofacial clefts: association with maternal hyperhomocysteinemia.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201187

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.EJHG.5201187

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

ResearchGate publication ID

0 references

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