Article ; Online: m
Epigenetics
2022 Volume 17, Issue 13, Page(s) 2278–2295
Abstract: Non-syndromic cleft lip with or without cleft palate (NSCLP), the most common human craniofacial malformation, is a complex disorder given its genetic heterogeneity and multifactorial component revealed by genetic, epidemiological, and epigenetic ... ...
Abstract | Non-syndromic cleft lip with or without cleft palate (NSCLP), the most common human craniofacial malformation, is a complex disorder given its genetic heterogeneity and multifactorial component revealed by genetic, epidemiological, and epigenetic findings. Epigenetic variations associated with NSCLP have been identified; however, functional investigation has been limited. Here, we combined a reanalysis of NSCLP methylome data with genetic analysis and used both |
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MeSH term(s) | Animals ; Humans ; Cleft Lip/genetics ; Cleft Palate/genetics ; Zebrafish/genetics ; Genetic Predisposition to Disease ; DNA Methylation ; Hypoxia/genetics ; Polymorphism, Single Nucleotide ; MicroRNAs/genetics |
Chemical Substances | MIRN152 microRNA, human ; MicroRNAs |
Language | English |
Publishing date | 2022-09-01 |
Publishing country | United States |
Document type | Journal Article ; Research Support, Non-U.S. Gov't |
ISSN | 1559-2308 |
ISSN (online) | 1559-2308 |
DOI | 10.1080/15592294.2022.2115606 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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