首页/数据集/Loss of <i>cup-2</i> activity in the germline is likely responsible for tumour suppression.

Loss of <i>cup-2</i> activity in the germline is likely responsible for tumour suppression.

NIAID Data Ecosystem2026-03-12 收录

数据链接：

https://figshare.com/articles/dataset/Loss_of_i_cup-2_i_activity_in_the_germline_is_likely_responsible_for_tumour_suppression_/16673335 数据链接链接失效反馈

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Loss of cup-2 activity in the germline is likely responsible for tumour suppression.

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创建时间：

2021-09-23

细胞染色质动态

肿瘤抑制机制

Cellular senescence is a stable proliferation arrest that suppresses tumorigenesis. Histone chaperone HIRA deposits nucleosome-destabilizing histone variant H3.3 into chromatin in a DNA replication-in

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SOLUTION NMR STRUCTURE OF TUMOR SUPPRESSOR P16INK4A, RESTRAINED MINIMIZED MEAN STRUCTURE

蛋白质结构解析

肿瘤抑制机制

SOLUTION NMR STRUCTURE OF TUMOR SUPPRESSOR P16INK4A, RESTRAINED MINIMIZED MEAN STRUCTURE Descriptor: TUMOR SUPPRESSOR P16INK4A Authors: Byeon, I.-J.L, Li, J, Ericson, K, Selby, T.L, Tevelev, A, Kim, H

Protein Data Bank Japan2024-05-22 更新50

Differentially expressed genes between the R-spodin2-overexpressing Huh-7 cell line and its negative control. Differentially expressed genes between the R-spodin2-overexpressing Huh-7 cell line and its negative control

差异基因表达分析

肿瘤抑制机制

To identify additional R-spodin2 target genes and the mechanisms behind its tumor-suppressive effect, we performed global microarray analysis of mRNA expression in a R-spodin2-overexpressing Huh-7 cel

NIAID Data Ecosystem30

Common Tumor Suppressive Signaling of Thyroid Hormone Receptor Beta in Breast and Thyroid Cancer Cells

肿瘤抑制机制

转录组学分析

The thyroid hormone receptor beta (TRÃ) is a tumor suppressor in multiple types of solid tumors, most prominently in breast and thyroid cancer. An increased understanding of the molecular mechanisms

NIAID Data Ecosystem90

PLTP is a p53 target gene with roles in cancer growth suppression and ferroptosis

肿瘤抑制机制

铁死亡调控

The tumor suppressor protein p53 suppresses cancer by regulating processes such as apoptosis, cell cycle arrest, senescence, and ferroptosis. Whereas numerous p53 target genes have been identified, o

NIAID Data Ecosystem50

Loss of <i>cup-2</i> activity in the germline is likely responsible for tumour suppression.

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