生物
CD8型
转录组
T细胞
基因
表型
免疫系统
基因表达
分子生物学
遗传学
CD3型
染色体
细胞
免疫学
作者
Nikita R. Raje,Janelle Noel‐MacDonnell,Katherine Shortt,Nicole M. Gigliotti,Marcia A. Chan,Daniel P. Heruth
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:2022-09-01
卷期号:209 (5): 874-885
被引量:5
标识
DOI:10.4049/jimmunol.2100346
摘要
≥ 0.8). We found significantly differentially expressed genes in participants with 22qDS compared with healthy control subjects and in participants with 22qDS with low T cell counts compared with those with normal T cell counts. Several enriched pathways suggest a role of T cells in defective communication between T cells and the innate immune system in 22qDS. Among these, the liver X receptor/retinoid X receptor pathway was noted to show several differentially expressed genes affecting participants with 22qDS compared with healthy control subjects and more so those with low T cell counts than in those with normal T cell counts.
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