Cargando…
Different Methylation of CpG-SNPs in Behcet's Disease
PURPOSE: We recently performed an Epigenome-Wide Association Studies (EWAS) study in Behcet's disease (BD) and identified various cytosine–phosphate–guanine (CpG) loci that were aberrantly methylated. In the current study, we wanted to investigate whether these sites contained genetic polymorph...
Autores principales: | Huang, Yang, Tan, Handan, Cao, Qingfeng, Yuan, Gangxiang, Su, Guannan, Yang, Peizeng |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541967/ https://www.ncbi.nlm.nih.gov/pubmed/31223615 http://dx.doi.org/10.1155/2019/3489305 |
Ejemplares similares
-
Genetic polymorphisms of C-type lectin receptors in Behcet’s disease in a Chinese Han population
por: Yang, Yi, et al.
Publicado: (2017) -
Functional Genetic Polymorphisms in the IL1RL1–IL18R1 Region Confer Risk for Ocular Behçet’s Disease in a Chinese Han Population
por: Tan, Xiao, et al.
Publicado: (2020) -
Changes in the Gut Microbiome Contribute to the Development of Behcet’s Disease via Adjuvant Effects
por: Wang, Qingfeng, et al.
Publicado: (2021) -
Ocular Behcet’s disease is associated with aberrant methylation of interferon regulatory factor 8 (IRF8) in monocyte-derived dendritic cells
por: Qiu, Yiguo, et al.
Publicado: (2017) -
Association of LACC1, CEBPB-PTPN1, RIPK2 and ADO-EGR2 with ocular Behcet’s disease in a Chinese Han population
por: Wu, Pengcheng, et al.
Publicado: (2018)