孟德尔随机化
下调和上调
效应器
生物
基因
细胞
孟德尔遗传
人口
遗传学
医学
免疫学
基因型
遗传变异
环境卫生
作者
Xiangwen Shi,Linmeng Tang,Mingjun Li,Yipeng Wu,Yongqing Xu
标识
DOI:10.2174/0113862073353509241205065221
摘要
This study conducted a comprehensive analysis of the potential link between OP and aging, identifying CD4+ TEM cells as the core cell subgroup in OP and aging samples. It further revealed the causal relationship between KLRB1, NR4A2, and S100A4 and the occurrence of OP. The upregulation of KLRB1 and S100A4 may contribute to OP pathogenesis by promoting interactions between CD4+ TEM cells and other cell subgroups, providing new insights for molecular targeting and immunotherapy of OP.
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