Additional file 8 of PATH-SURVEYOR: pathway level survival enquiry for immuno-oncology and drug repurposing

NIAID Data Ecosystem2026-05-01 收录

数据链接：

https://figshare.com/articles/dataset/Additional_file_8_of_PATH-SURVEYOR_pathway_level_survival_enquiry_for_immuno-oncology_and_drug_repurposing/23597440 数据链接链接失效反馈

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资源简介：

Additional file 8. Supplementary Table S1–S4.

创建时间：

2023-06-28

肿瘤免疫组化数据分析

肿瘤免疫学

生物信息学

免疫组织化学（immunohistochemistry, IHC）是利用抗原抗体反应已显示某蛋白的表达及定位的实验。这种实验的独特之处在于它既直观的显示了蛋白在组织及细胞或细胞亚结构的定位，又保留了组织样品的结构特征。本产品用于批量组化产品分析，主要比较差异分析，生存分析，Cox分析，fisher分析。同时绘制生存曲线， Cox曲线。

上海数据交易所2024-11-19 更新120

In-silico identification of novel DDI2 inhibitor in glioblastoma via repurposing FDA approved drugs using molecular docking and MD simulation study

药物再利用

癌症治疗

Glioblastoma, the most severe form of brain tumor and a leading cause of death within a year of diagnosis, is characterized by excessive protein synthesis and folding in the lumen of the endoplasmic r

DataCite Commons2023-05-04 更新60

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

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 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

Additional file 8 of PATH-SURVEYOR: pathway level survival enquiry for immuno-oncology and drug repurposing

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