Your browser doesn't support javascript.
loading
Identification of Target Genes at Juvenile Idiopathic Arthritis GWAS Loci in Human Neutrophils.
Li, Junyi; Yuan, Xiucheng; March, Michael E; Yao, Xueming; Sun, Yan; Chang, Xiao; Hakonarson, Hakon; Xia, Qianghua; Meng, Xinyi; Li, Jin.
Affiliation
  • Li J; Department of Cell Biology, 2011 Collaborative Innovation Center of Tianjin for Medical Epigenetics, Tianjin Key Laboratory of Medical Epigenetics, Tianjin Medical University, Tianjin, China.
  • Yuan X; Department of Cell Biology, 2011 Collaborative Innovation Center of Tianjin for Medical Epigenetics, Tianjin Key Laboratory of Medical Epigenetics, Tianjin Medical University, Tianjin, China.
  • March ME; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA, United States.
  • Yao X; Department of Cell Biology, 2011 Collaborative Innovation Center of Tianjin for Medical Epigenetics, Tianjin Key Laboratory of Medical Epigenetics, Tianjin Medical University, Tianjin, China.
  • Sun Y; Department of Cell Biology, 2011 Collaborative Innovation Center of Tianjin for Medical Epigenetics, Tianjin Key Laboratory of Medical Epigenetics, Tianjin Medical University, Tianjin, China.
  • Chang X; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA, United States.
  • Hakonarson H; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA, United States.
  • Xia Q; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, United States.
  • Meng X; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
  • Li J; Department of Cell Biology, 2011 Collaborative Innovation Center of Tianjin for Medical Epigenetics, Tianjin Key Laboratory of Medical Epigenetics, Tianjin Medical University, Tianjin, China.
Front Genet ; 10: 181, 2019.
Article in En | MEDLINE | ID: mdl-30972099
ABSTRACT
Juvenile idiopathic arthritis (JIA) is the most common chronic rheumatic disease among children which could cause severe disability. Genomic studies have discovered substantial number of risk loci for JIA, however, the mechanism of how these loci affect JIA development is not fully understood. Neutrophil is an important cell type involved in autoimmune diseases. To better understand the biological function of genetic loci in neutrophils during JIA development, we took an integrated multi-omics approach to identify target genes at JIA risk loci in neutrophils and constructed a protein-protein interaction network via a machine learning approach. We identified genes likely to be JIA risk loci targeted genes in neutrophils which could contribute to JIA development.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies Language: En Journal: Front Genet Year: 2019 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies Language: En Journal: Front Genet Year: 2019 Document type: Article Affiliation country: China