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H-RasG12V-Expressing BAR-T p53RNAi Cells Are Tumorigenic In Vivo.

Figshare2015-12-02 更新2026-04-29 收录

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https://figshare.com/articles/dataset/_H_Ras_G12V_Expressing_BAR_T_p53RNAi_Cells_Are_Tumorigenic_In_Vivo_/498270 数据链接链接失效反馈

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H-RasG12V-Expressing BAR-T p53RNAi Cells Are Tumorigenic In Vivo.

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创建时间：

2015-12-02

基因表达分析

肿瘤发生机制

We compared lung mRNA expression profiles between RAG1-/- control and RAG1-/- Sgo1-/+ chromosome instability model mice. RAG1-/-Sgo1-/+ mice developed significantly more spontaneous lung tumors. Char

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Identification of a novel TINCR-EGFR signaling pathway loop which initiates receptor tyrosine kinases cascade and confers tumorigenesis in human cancer

癌症信号通路

肿瘤发生机制

RNA sequencing was performed to investigate the potential crosstalk between TINCR and microRNAs. Overall design: microRNA profiles of T47D with TINCR knockdown and scramble were generated by deep sequ

NIAID Data Ecosystem50

Expression of FUS-CHOP fusion protein in immortalized/transformed human Mesenchymal Stem Cells drives mixoid liposarcoma formation

黏液样脂肪肉瘤

肿瘤发生机制

Although different sarcomas have been modeled in mice upon expression of fusion oncogenes in MSCs, sarcomagenesis has not been successfully modeled in human MSCs (hMSCs). We report that FUS-CHOP, a ha

NIAID Data Ecosystem40

Summary of the mutations identified in positive control samples.

基因突变验证

实验质量控制

Summary of the mutations identified in positive control samples.

Figshare2017-07-27 更新50

Wnt-Induced Stabilization of KDM4C Is Required for Wnt/beta-Catenin Target Gene Expression and Tumorigenesis

Wnt信号通路表观遗传

肿瘤发生机制

Wnt/beta-catenin signaling is essential for stem cell regulation and cancer formation by activation of target genes transcription. For transcriptional activation, the histone around promoters needs to

NIAID Data Ecosystem40

H-RasG12V-Expressing BAR-T p53RNAi Cells Are Tumorigenic In Vivo.

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