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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Oral Diseasesarrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Oral Diseases
Article . 2018 . Peer-reviewed
License: Wiley Online Library User Agreement
Data sources: Crossref
Oral Diseases
Article . 2019
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Association of long interspersed nucleotide element‐1 and interferon regulatory factor 6 methylation changes with nonsyndromic cleft lip with or without cleft palate

Authors: Yanhua Li; Ying Deng; Changfei Deng; Liang Xie; Li Yu; Lijun Liu; Yumei Yuan; +2 Authors

Association of long interspersed nucleotide element‐1 and interferon regulatory factor 6 methylation changes with nonsyndromic cleft lip with or without cleft palate

Abstract

AbstractObjectiveTo examine the possible associations between methylation changes in the promoter regions of long interspersed nucleotide element‐1 (LINE‐1) and interferon regulatory factor 6 gene (IRF6) and nonsyndromic cleft lip with or without cleft palate (NSCL/P).MethodsA case–control investigation was performed to compare 37 infants affected by NSCL/Ps with 60 babies without cleft malformations. Their genomic DNA samples were obtained, and the LINE‐1 and IRF6 methylation levels were measured by using Sequenom MassArray. Unconditional logistic regression was adopted to estimate the odds ratio.ResultsInfants with NSCL/Ps had a higher methylation level at LINE‐1 and IRF6 promoter regions than controls. High levels of LINE‐1 (≥64.07%) and IRF6 (≥6.46%) methylation were associated with an increased risk of NSCL/P (LINE‐1, OR = 2.63, 95% CI: 1.07–6.57; IRF6, OR = 4.73, 95% CI: 2.10–13.07), and the associations remained to be significant after adjusting for potential confounders. Similar associations were also found for cleft lip only, cleft lip, and palate.ConclusionOur study suggested that aberrant methylation of LINE‐1 and IRF6 might contribute to the development of NSCL/Ps. Further studies are needed to replicate the findings.

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Keywords

Male, Genotype, Cleft Lip, Infant, DNA Methylation, Polymorphism, Single Nucleotide, Cleft Palate, Long Interspersed Nucleotide Elements, Case-Control Studies, Interferon Regulatory Factors, Humans, Female, Genetic Predisposition to Disease, Promoter Regions, Genetic

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
6
Top 10%
Average
Average
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