Expression data from murine intestinal tissue upon depletion of regulatory T cells

ChEBI2013-07-10 更新2026-07-21 收录

肠道微环境

调节性T细胞功能

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Expression data from murine intestinal tissue upon depletion of regulatory T cells

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2013-07-10

Transcription profile of WT and LKB1 (encoded by the gene Stk11)-deficient Treg cells. Mus musculus

调节性T细胞功能

免疫细胞转录组学

LKB1 deficiency in Treg cells impairs their survival, metabolism and suppressive function. To exclude the impact of excessive inflammation on LKB1-deficient Treg cells, we generated mixed bone marrow

NIAID Data Ecosystem50

Transepithelial barrier dysfunction drives microbiota dysbiosis to initiate epithelial clock-driven inflammation [gene expression]

肠道微环境

微生物组时序分析

A time-series alteration in fecal microbiota was linked to the emergence of intraepithelial bacteria and a unique transcriptome profile in the mouse colon during IBD development. Use of gene array to

NIAID Data Ecosystem10

Comparing the transcriptome of small intestinal epithelial cells in organoids after co-culture with NKT cells

肠道微环境

器官转录组学

Intestinal homeostasis is maintained through the combined functions of epithelial and immune cells that collaborate to preserve the integrity of the intestinal barrier. However, the mechanisms by whic

NIAID Data Ecosystem00

Human Regulatory T Cell Suppressive Function Is Independent of Apoptosis Induction in Activated Effector T Cells

调节性T细胞功能

自身免疫疾病机制

BackgroundCD4+CD25+FOXP3+ Regulatory T cells (Treg) play a central role in the immune balance to prevent autoimmune disease. One outstanding question is how Tregs suppress effector immune responses in

NIAID Data Ecosystem40

Functional Analysis and Gene Expression Profile of Umbilical Cord Blood Regulatory T Cells. Homo sapiens

调节性T细胞功能

脐带血免疫调节

Since the role of cord blood (CB) regulatory T cells (Tregs) for the suppression of the allogeneic T-cell response is under investigation, we analyzed and compared the functional properties and gene e

NIAID Data Ecosystem10

Expression data from murine intestinal tissue upon depletion of regulatory T cells

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