IndraLab

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USP10 translocates to the nucleus. 31 / 31
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sparser
"Alternatively, USP10 could translocate into the nucleus to participate in DNA damage response."

sparser
"After DNA damage, USP10 is stabilised, and a fraction of USP10 translocates to the nucleus to activate p53."

sparser
"USP10 is upregulated and translocates to the nucleus following DNA damage and regulates p53-dependent DNA damage response."

sparser
"Interestingly USP10, a predominantly cytoplasmic DUB, is involved in homeostasis of cytoplasmic p53 in unstressed cells, but, following DNA damage, a fraction of USP10 can translocate into the nucleus where it contributes to p53 activation [ xref ]."

sparser
"Upon DNA damage, USP10 can translocate to the nucleus and also contribute to p53 activation xref xref ."

sparser
"Following DNA damage, USP10 also translocates to the nucleus and contributes to p53 activation."

sparser
"For example, USP10, a cytoplasmic DUB, translocates to the nucleus upon DNA damage where it contributes to the stabilization of p53 [ xref ]."

reach
"This process is very important during DNA-damage response, in which USP10 translocates to the nucleus and deubiquitinates p53, stabilizing it and thus regulating its response to DNA damage [113,114,115]."

sparser
"Following DNA damage, phosphorylation of USP10 by ATM leads to translocation of USP10 into the nucleus, where USP10 deubiquitinates and stabilizes nuclear p53 [ xref ]."

sparser
"Upon induction by DNA damage, a fraction of USP10 is phosphorylated by ATM and translocates to the nucleus where it deubiquitinates p53."

sparser
"Following DNA damage, a fraction of USP10 translocates to the nucleus and contributes to p53 activation."

reach
"Here, we demonstrated that a deubiquitinase USP10, which specifically stabilizes nuclear AID protein, can translocate into the nucleus after AKT-mediated phosphorylation at its T674 within the NLS domain."

reach
"Yuan et al. demonstrated that ATM could phosphorylate USP10 at Thr42 and Ser337 upon the DNA-damage response and USP10 was translocated into the nucleus, where the N-terminus of USP10 (amino acids 1–100) binds to p53 and inhibits its ubiquitination [27]."

sparser
"Following DNA damage, USP10 is stabilized and a fraction of USP10 translocates to the nucleus to activate p53."

sparser
"Yuan et al. demonstrated that ATM could phosphorylate USP10 at Thr42 and Ser337 upon the DNA-damage response and USP10 was translocated into the nucleus, where the N-terminus of USP10 (amino acids 1-100) binds to p53 and inhibits its ubiquitination [27] ."

reach
"Following DNA damage, USP10 also translocates to the nucleus and contributes to p53 activation."

reach
"USP10 is upregulated and translocates to the nucleus following DNA damage and regulates p53 dependent DNA damage response."

sparser
"After DNA damage, USP10 is stabilized, and a fraction of USP10 translocates to the nucleus to activate p53."

reach
"Under DNA damage, USP10 becomes stabilization and translocates to the nucleus to activate and stabilize nuclear p53."

sparser
"This process is very important during the DNA-damage response, when USP10 translocates to the nucleus and deubiquitinates p53, stabilizing it and thus regulating its response to DNA damage ( xref )."

reach
"In the case of DNA damage, USP10 is stabilized and translocates to the nucleus to activate and stabilize p53."

sparser
"This process is very important during DNA-damage response, in which USP10 translocates to the nucleus and deubiquitinates p53, stabilizing it and thus regulating its response to DNA damage [ xref , xref , xref ]."

sparser
"We also show that following genotoxic stress, a fraction of USP10 translocates to the nucleus, and this translocation is required for the stabilization and activation of p53."

sparser
"Under DNA damage, USP10 becomes stabilization and translocates to the nucleus to activate and stabilize nuclear p53."

reach
"USP10 translocates to the nucleus, aiding deubiquitination of p53 by USP7."

reach
"Upon DNA damage, USP10 can translocate to the nucleus and also contribute to p53 activation XREF_BIBR XREF_BIBR."

sparser
"Here, we demonstrated that a deubiquitinase USP10, which specifically stabilizes nuclear AID protein, can translocate into the nucleus after AKT-mediated phosphorylation at its T674 within the NLS domain."

sparser
"Following DNA damage, a fraction of USP10 translocates to the nucleus and contributes to p53 activation ( xref )."

sparser
"However, following DNA damage, part of USP10 translocate into nucleus to deubiquitylate p53 and thus boost p53 activation."

sparser
"Our results suggest that p53 is still ubiquitinated by residual Mdm2/Mdmx activity following DNA damage ( xref ), and the nuclear translocation of USP10 could further boost p53 activation."

sparser
"Following DNA damage or other genotoxic stress, a fraction of cytoplasmic USP10 is translocated into the nucleus, which is necessary for the activation and stabilization of p53."