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Human bone and marrow niche formation by mesenchymal progenitors in vivo is predefined by an organotypic epigenetic signature

ChEBI2015-02-04 更新2026-07-21 收录

骨髓微环境

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数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-41933 数据链接链接失效反馈

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Human bone and marrow niche formation by mesenchymal progenitors in vivo is predefined by an organotypic epigenetic signature

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创建时间：

2015-02-04

胰腺癌耐药机制

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ObjectivePancreatic cancer is associated with poor prognosis and dismal survival rates. This study aims to investigate roles of lncRNA UCA1-loaded exosomes secreted by pancreatic stellate cells (PSCs)

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SAM domain polymerization links subnuclear clustering of PRC1 to silencing detected using expression data and ChIP experiments

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染色质构象

Polycomb group (PcG) proteins mediate heritable but reversible silencing of developmental regulator genes by modifying their chromatin configuration. Accumulating evidence documents a role for PcG pro

NIAID Data Ecosystem20

Additional file 7 of Conservation and trans-regulation of histone modification in the A and B subgenomes of polyploid wheat during domestication and ploidy transition

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H3K27me3修饰分析

Additional file 7: Table S6. Gene Ontology (GO) enrichment terms and genes used for GO analysis of H3K27me3 modification in WTW → DTW → ETW process.

NIAID Data Ecosystem10

Gene expression profiles of Chronic kidney disease

慢性肾病基因表达

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Epidemiological studies indicate that adverse intrauterine and postnatal environment has a long-lasting role in chronic kidney disease (CKD) development. Epigenetic information can represent a plausib

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Table_2_DNA Damage Induces Dynamic Associations of BRD4/P-TEFb With Chromatin and Modulates Gene Transcription in a BRD4-Dependent and -Independent Manner.DOCX

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应激基因表达

The bromodomain-containing protein BRD4 has been thought to transmit epigenetic information across cell divisions by binding to both mitotic chromosomes and interphase chromatin. UV-released BRD4 medi

NIAID Data Ecosystem10

Human bone and marrow niche formation by mesenchymal progenitors in vivo is predefined by an organotypic epigenetic signature

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