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Deletion of human tarbp2 reveals cellular microRNA targets and cell cycle function of TRBP

ChEBI2014-09-16 更新2026-07-21 收录

microRNA靶点分析

细胞周期机制

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-61458 数据链接链接失效反馈

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Deletion of human tarbp2 reveals cellular microRNA targets and cell cycle function of TRBP

应用场景：

创建时间：

2014-09-16

细胞周期机制

癌症分子生物学

Loss-of-function mutations of p16(INK4a) have been identified in a large number of human tumors. An established biochemical function of p16 is its ability to specifically inhibit cyclin D-dependent ki

PubMed Central80

Nuclear Myosin 1c Facilitates the Chromatin Modifications Required to Activate rRNA Gene Transcription and Cell Cycle Progression

rRNA调控

细胞周期机制

Actin and nuclear myosin 1c (NM1) cooperate in RNA polymerase I (pol I) transcription. NM1 is also part of a multiprotein assembly, B-WICH, which is involved in transcription. This assembly contains t

NIAID Data Ecosystem70

Cell cycle-dependent YTHDF2 promotes mitotic entry by repressing WEE1

m6ARNA修饰调控

细胞周期机制

The m6A modification regulates mRNA stability and translation. Here we show that transcriptomic m6A modification is dynamic and the m6A reader protein YTHDF2 promotes mRNA decay during the cell cycle.

NIAID Data Ecosystem40

Transcription profiling by array of human bone metastatic breast cancer cells following miRNA and siRNA transfection

乳腺癌分子机制

microRNA靶点分析

Identification of MicroRNAs Inhibiting TGF-beta-Induced IL-11 Production in Bone Metastatic Breast Cancer Cells

NIAID Data Ecosystem70

Table_4_E2F1 Induces KIF26A Transcription and Promotes Cell Cycle Progression via CDK–RB–E2Fs Feedback Loop in Breast Cancer.docx

乳腺癌基因

细胞周期机制

ObjectiveThe aim of this study was to investigate the role of KIF26A in breast cancer. MethodqRT-PCR and immunohistochemistry were conducted to explore KIF26A expression and functional contribution to

NIAID Data Ecosystem60

Deletion of human tarbp2 reveals cellular microRNA targets and cell cycle function of TRBP

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