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VprBP has been implicated in transcriptionally silent chromatin formation and cell cycle regulation, but the molecular basis underlying such effects remains unclear. To investigate the role of VprBP on gene regulation, genme-wide gene expression analysis is carried out in DU145 cells expressing eith...
ORGANISM(S): Homo sapiens 
VprBP regulates osteoclast differentiation via histone H2A phosphorylation
Here, we identify the USP2 (ubiquitin specific peptidase 2)-VPRBP (viral protein R binding protein) axis as a new pathway for p53 regulation. Like Mdm2 (Mouse double minute 2), VPRBP is a potent repressor of p53 but VPRBP stability is controlled by USP2. Interestingly, the USP2-VPRBP axis is also i...
ORGANISM(S): Homo sapiens (Human) 
2023-03-15 | PXD040477 | Pride
Here, we identify the USP2 (ubiquitin specific peptidase 2)-VPRBP (viral protein R binding protein) axis as a new pathway for p53 regulation. Like Mdm2 (Mouse double minute 2), VPRBP is a potent repressor of p53 but VPRBP stability is controlled by USP2. Interestingly, the USP2-VPRBP axis is also i...
ORGANISM(S): Homo sapiens (Human) 
2023-03-15 | PXD040473 | Pride
VprBP directs epigenetic gene silencing through H2A phosphorylation in colon cancer
Bone remodeling is a continuous and balanced process which relies on the dynamic equilibrium between osteoclastic bone resorption and osteoblastic bone formation. During osteoclast differentiation, pro-osteoclastogenic and anti-osteoclastogenic genes are selectively targeted by positive and negative...
ORGANISM(S): Mus musculus 
2025-01-28 | GSE275603 | GEO
VprBP has been implicated in transcriptionally silent chromatin formation and cell cycle regulation, but the molecular basis underlying such effects remains unclear. To investigate the role of VprBP on gene regulation, genme-wide gene expression analysis is carried out in DU145 cells expressing eith...
ORGANISM(S): Homo sapiens 
2013-11-07 | GSE50414 | GEO
Phosphorylation and stabilization of EZH2 by VprBP trigger aberrant gene silencing in colon cancer
Identification of highly potent inhibitors capable of blocking VprBP kinase activity and suppressing prostate tumor growth
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