首页/数据集/Decitabine disrupts EBV genomic epiallele DNA methylation patterns around CTCF binding sites to increase chromatin accessibility and lytic transcription in gastric cancer

Decitabine disrupts EBV genomic epiallele DNA methylation patterns around CTCF binding sites to increase chromatin accessibility and lytic transcription in gastric cancer

NIAID Data Ecosystem2026-05-01 收录

EBV潜伏感染

表观遗传治疗

数据链接：

https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE239770 数据链接链接失效反馈

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资源简介：

This SuperSeries is composed of the SubSeries listed below. Refer to individual Series

应用场景：

创建时间：

2023-12-07

癌症分子机制

表观遗传治疗

Nupr1 is a chromatin protein which cooperates with KrasG12D to induce PanIN formation in mice, though the molecular mechanisms underlying this effect remain to be fully characterized. In the current s

NIAID Data Ecosystem70

Epstein-Barr Virus facilitates KLF14 expression by regulating the cooperative binding of E2F-Rb-HDAC in latent infection. Epstein-Barr Virus facilitates KLF14 expression by regulating the cooperative binding of E2F-Rb-HDAC in latent infection

EBV潜伏感染

转录调控机制

Epstein-Barr Virus facilitates KLF14 expression by regulating the cooperative binding of E2F-Rb-HDAC in latent infection Overall design: Examination of E2F6, E2F1, Rb, HDAC1, and HDAC2 binding feature

NIAID Data Ecosystem50

Differential Regulation of Epstein-Barr Virus (EBV) Latent Gene Expression in Burkitt Lymphoma Cells Infected with a Recombinant EBV Strain

EBV潜伏感染

Burkitt淋巴瘤病理诊断

Epstein-Barr virus (EBV)-negative Burkitt lymphomas (BLs) can be infected in vitro with prototype EBV strains to study how the virus may affect the phenotype of tumor cells. Studies thus far have conc

PubMed Central40

Supporting data for 'Epstein-Barr virus BART lncRNAs induce IKZF3/Aiolos to maintain EBV latency and promote tumorigenicity in nasopharyngeal carcinoma'

鼻咽癌临床病理

EBV潜伏感染

The datasets contains raw data for three result chapters of my thesis, which are chapter 3, 4 and 5. These rawdata were utilized to generate the results for three chapters. The raw data of chapter 3 c

DataCite Commons2022-08-22 更新60

Multiplex Epigenome Editing of MECP2 to Rescue Rett Syndrome Neurons [ChIP-BS-Seq]

表观遗传治疗

Rett综合征神经元模型

Rett syndrome (RTT) is an X-linked neurodevelopmental disorder caused by loss-of-function heterozygous mutations of MECP2. Reactivation of the silent wild-type MECP2 allele on the inactive X chromosom

NIAID Data Ecosystem50

Decitabine disrupts EBV genomic epiallele DNA methylation patterns around CTCF binding sites to increase chromatin accessibility and lytic transcription in gastric cancer

资源简介：

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