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Supplementary File 1 from Control of Breast Cancer Growth and Initiation by the Stem Cell–Associated Transcription Factor TCF3

Figshare2012-11-01 更新2026-04-28 收录

乳腺癌分子机制

Wnt信号通路

数据链接：

https://figshare.com/articles/dataset/Supplementary_File_1_from_Control_of_Breast_Cancer_Growth_and_Initiation_by_the_Stem_Cell_Associated_Transcription_Factor_TCF3/22393335 数据链接链接失效反馈

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PDF file - 33K, Wnt-responsive genes

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创建时间：

2012-11-01

乳腺癌分子机制

表观遗传学分析

Comparison between our T-47D DNase-seq data and analogous data from ENCODE. DNase-seq peaks from promoter regions in BMP4-treated and vehicle-treated T-47D cells were compared to DNase-seq data of T-4

NIAID Data Ecosystem130

Additional file 1: of Inferring miRNA sponge co-regulation of protein-protein interactions in human breast cancer

乳腺癌分子机制

RNA调控网络

BRCA-related miRNA sponge interaction network. The network includes 37076 miRNA sponge interactions. (XLSX 484Â kb)

NIAID Data Ecosystem70

KCTD15 Is Overexpressed in her2+ Positive Breast Cancer Patients and Its Silencing Attenuates Proliferation in SKBR3 CELL LINE

乳腺癌分子机制

基因功能验证

Scientific research for publishing the article

Mendeley Data2024-01-31 更新40

衰老生物学

Wnt信号通路

Purpose: Characterize functional alterations in stem cells and paneth cells obtained from young and aged mice, focusing on age-based impairment of intestinal regeneration due to a decline in canonical

NIAID Data Ecosystem100

Dietary ligands diindolylmethane and resveratrol result in diverse ERα signaling not seen after E2 and a subset of diindolylmethane mediated signaling needs concurrent AHR activation.. Dietary ligands diindolylmethane and resveratrol result in diverse ERα signaling not seen after E2 and a subset of diindolylmethane mediated signaling needs concurrent AHR activation.

乳腺癌分子机制

受体信号通路

Inhibitory crosstalk between estrogen receptor alpha (ER alpha ) and aryl hydrocarbon receptor (AHR) regulates 17-estradiol (E2)-dependent breast cancer cell signaling. ER alpha and AHR are transcript

NIAID Data Ecosystem40

Supplementary File 1 from Control of Breast Cancer Growth and Initiation by the Stem Cell–Associated Transcription Factor TCF3

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