HDAC Inhibitors induce tumor cell-selective pro-apoptotic transcriptional responses.

ChEBI2013-04-22 更新2026-07-21 收录

肿瘤药物机制

转录组学分析

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https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-43010 数据链接链接失效反馈

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HDAC Inhibitors induce tumor cell-selective pro-apoptotic transcriptional responses.

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2013-04-22

Transcriptomic comparison of FVB mouse strain lung Cells and epithelial trachea cells.. Mus musculus

转录组学分析

小鼠肺部细胞研究

We injected 12 (6 males, 6 females) FVB mice 8 weeks old, with either saline or urethane. One week later we sacrificed and harvested their lungs. The dissected lungs were assayed to RNA extraction (vi

NIAID Data Ecosystem40

Clostridium_difficile_transcriptomics__sporulation_

艰难梭菌孢子形成机制

转录组学分析

Clostridium difficile is a Gram-positive, sporogenic anaerobe that is rapidly emerging as an important nosocomial enteric pathogen1,2. C. difficile is also the primary causative agent of antibiotic-a

NIAID Data Ecosystem20

Transcriptomic profiling of naïve and memory phenotype CD8 T cells in Dock2-deficient mice. Transcriptomic profiling of naïve and memory phenotype CD8 T cells in Dock2-deficient mice

T细胞免疫学

转录组学分析

Transcriptomic data linked to our study showing that DOCK2 sets the threshold for entry into the virtual memory CD8+ T cell compartment by negatively regulating tonic TCR triggering Overall design: RN

NIAID Data Ecosystem10

Additional file 11: Table S6. of Transcriptome profiling of a spirodiclofen susceptible and resistant strain of the European red mite Panonychus ulmi using strand-specific RNA-seq

害虫抗药性机制

转录组学分析

Annotation details and accession numbers of ATP-binding cassette family transporters. (XLSX 441 kb)

Figshare2016-12-14 更新20

Cucumis melo cultivar:MR-1 Raw sequence reads. Cucumis melo cultivar:MR-1

甜瓜白粉病

转录组学分析

This study may provide a new understanding of the molecular mechanisms of melon resistance to powdery mildew based on our results revealed both similar and differential patterns of gene expression bet

NIAID Data Ecosystem20

HDAC Inhibitors induce tumor cell-selective pro-apoptotic transcriptional responses.

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