Sentence and cancer type
Showing 41-60 of 71 items.
SentenceCancertype
have demonstrated that the lymphoid leukemia-associated protein, PAX5-PML chimeric oncogenic protein, could bind to PAX5 response-element as homodimer to inhibit the transactivation of PAX5 target-genesleukemia,
Our findings unveil a novel essential oncogenic activity of PML/RARA in Acute promyelocitic leukemialeukemia,
The PML/RAR alpha oncoprotein is a direct molecular target of retinoic acid in acute promyelocytic leukemia cells. leukemia,
An arenavirus RING (zinc-binding) protein binds the oncoprotein promyelocyte leukemia protein (PML) and relocates PML nuclear bodies to the cytoplasm. leukemia,
Modulation of CREB binding protein function by the promyelocytic (PML) oncoprotein suggests a role for nuclear bodies in hormone signaling. None
Human Daxx regulates Fas-induced apoptosis from nuclear PML oncogenic domains (PODs). None
PML regulates p53 acetylation and premature senescence induced by oncogenic Ras. None
PML is induced by oncogenic ras and promotes premature senescence. None
PML and the oncogenic nuclear domains in regulating transcriptional repression. None
Colocalization and heteromerization between the two human oncogene POZ/zinc finger proteins, LAZ3 (BCL6) and PLZF. None
Proteasome-independent disruption of PML oncogenic domains (PODs), but not covalent modification by SUMO-1, is required for human cytomegalovirus immediate-early protein IE1 to inhibit PML-mediated transcriptional repression. None
Pathways of retinoic acid- or arsenic trioxide-induced PML/RARalpha catabolism, role of oncogene degradation in disease remission. None
Identification of PML oncogenic domains (PODs) in human megakaryocytes. None
Recruitment of NBS1 into PML oncogenic domains via interaction with SP100 protein. None
Distinct nuclear body components, PML and SMRT, regulate the trans-acting function of HTLV-1 Tax oncoprotein. None
ZIP kinase triggers apoptosis from nuclear PML oncogenic domains. None
The fusion oncoprotein PML-RARalpha induces endoplasmic reticulum (ER)-associated degradation of N-CoR and ER stress. None
interference by human Cytomegalovirus IE1 protein with both the sumoylation of PML and its repressor activity requires a physical interaction with PML that also leads to disruption of PML oncogenic domains (PODs).None
inhibition of monocyte differentiation all contribute to the oncogenic activity of PML-RARalphaNone
RXR is an essential component of the oncogenic PML/RARA complex in vivo. None