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Supplementary Tables from Protection of Regulatory T Cells from Fragility and Inactivation in the Tumor Microenvironment

NIAID Data Ecosystem2026-04-30 收录

肿瘤免疫学

调节性T细胞功能

数据链接：

https://figshare.com/articles/dataset/Supplementary_Tables_from_Protection_of_Regulatory_T_Cells_from_Fragility_and_Inactivation_in_the_Tumor_Microenvironment/30720664 数据链接链接失效反馈

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资源简介：

Supplementary Tables 1, 2, and 3

应用场景：

创建时间：

2022-12-02

肿瘤免疫学

T细胞受体库

Identification of tumor-specific effects on peripheral TCRÃŽÂ² repertoire formation in humans, investigation of the clonal origin of regulatory T cells in breast cancer patients and impact analysis of

NIAID Data Ecosystem100

Transcriptome analysis of tumor infiltrating NK and T cells in CT26-bearing BALB/C mice

肿瘤免疫学

肿瘤浸润淋巴细胞

CT26 tumors were implanted subcutaneously into syngeneic BALB/C mice and allowed to grow for 15-25 days. Tumors were collected, mechanically dissociated, and immune cells enriched using Percoll gradie

NIAID Data Ecosystem60

Table_2_Proportional Tumor Infiltration of T Cells via Circulation Duplicates the T Cell Receptor Repertoire in a Bilateral Tumor Mouse Model.xlsx

肿瘤免疫学

T细胞受体库

Temporal analysis of the T cell receptor (TCR) repertoire has been used to monitor treatment-induced changes in antigen-specific T cells in patients with cancer. However, the lack of experimental mode

NIAID Data Ecosystem50

肿瘤免疫学

基因调控

Genes related to immune suppression that are negatively regulated by DMHCA in tumors from NeuT/ATTAC+AP mice.

NIAID Data Ecosystem60

Transcriptome of CD8+T-cells from C57BL/6 mice in induced tumor-like conditions along with IL-2 and IL-12.. Transcriptome of CD8+T-cells from C57BL/6 mice in induced tumor-like conditions along with IL-2 and IL-12.

肿瘤免疫学

细胞基因表达

To study differentially expressed genes via RNA seq analysis of CD8+T-cells from C57BL/6 mice splenocytes treated with the four different conditions: IL-2, IL-2 80%TCM, IL-12 and IL-12 80%TCM. (TCM =

NIAID Data Ecosystem60

Supplementary Tables from Protection of Regulatory T Cells from Fragility and Inactivation in the Tumor Microenvironment

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