Decreased sphingolipid synthesis in children with 17q21 asthma–risk genotypes
Author:
Funder
National Center for Advancing Translational Sciences of the National Institutes of Health
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Link
https://www.jci.org/articles/view/130860/files/pdf
Reference32 articles.
1. Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma
2. Risk of childhood asthma is associated with CpG-site polymorphisms, regional DNA methylation and mRNA levels at the GSDMB/ORMDL3 locus
3. Allele-Specific Chromatin Remodeling in the ZPBP2/GSDMB/ORMDL3 Locus Associated with the Risk of Asthma and Autoimmune Disease
4. A decade of research on the 17q12-21 asthma locus: Piecing together the puzzle
5. Asthma-associated polymorphisms in 17q21 influence cord blood ORMDL3 and GSDMA gene expression and IL-17 secretion
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