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The goal of the current study is to identify intracellular notch1 icn1, the activated form of notch1 binding. Here, we demonstrate that stress signals elicited by proinflammatory cytokines and lipopolysaccharides lead to the degradation of foxp3 through the action of the e3 ubiquitin ligase stub1. Pzhpv7 cells were maintained in keratinocyte serumfree medium ksfm. Knockdown of endogenous stub1 or hsp70 prevented foxp3 degradation. Hsp70 interacts with stub1 and controls protein stabilization. Notch1 deregulation is assuming a focal role in tcell acute lymphoblastic leukemia tall. Download a free trial for realtime bandwidth monitoring, alerting, and more.
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