The interaction of Pax5 (BSAP) with Daxx can result in transcriptional activation in B cells
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Homeodomain-interacting protein kinase 1 modulates Daxx localization, phosphorylation, and transcriptional activity.Daxx silencing sensitizes cells to multiple apoptotic pathwaysEBV tegument protein BNRF1 disrupts DAXX-ATRX to activate viral early gene transcriptionThe death domain-associated protein modulates activity of the transcription co-factor Skip/NcoA62Physiological and functional interactions between Tcf4 and Daxx in colon cancer cellsNegative modulation of androgen receptor transcriptional activity by DaxxThe ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodiesConditional knockout mice reveal distinct functions for the global transcriptional coactivators CBP and p300 in T-cell developmentInactivating a cellular intrinsic immune defense mediated by Daxx is the mechanism through which the human cytomegalovirus pp71 protein stimulates viral immediate-early gene expressionA novel human Ada2 homologue functions with Gcn5 or Brg1 to coactivate transcriptionGlobal transcriptional coactivators CREB-binding protein and p300 are highly essential collectively but not individually in peripheral B cellsSignal transducer and activator of transcription 3 regulation by novel binding partnersPromyelocytic leukemia protein (PML) functions as a glucocorticoid receptor co-activator by sequestering Daxx to the PML oncogenic domains (PODs) to enhance its transactivation potentialThe transcription factor Pax5 regulates its target genes by recruiting chromatin-modifying proteins in committed B cellsDaxx inhibits muscle differentiation by repressing E2A-mediated transcriptionAdenovirus type 5 early region 1B 55K oncoprotein-dependent degradation of cellular factor Daxx is required for efficient transformation of primary rodent cellsSUMO modification negatively modulates the transcriptional activity of CREB-binding protein via the recruitment of Daxx.IFN-zeta/ limitin: a member of type I IFN with mild lympho-myelosuppression.Viral reprogramming of the Daxx histone H3.3 chaperone during early Epstein-Barr virus infection.Histone acetyltransferase p300 acetylates Pax5 and strongly enhances Pax5-mediated transcriptional activityCharacterizing the N- and C-terminal Small ubiquitin-like modifier (SUMO)-interacting motifs of the scaffold protein DAXX.DNA damage-induced regulatory interplay between DAXX, p53, ATM kinase and Wip1 phosphatase.Body language: the function of PML nuclear bodies in apoptosis regulation.Dynamic changes in binding of immunoglobulin heavy chain 3' regulatory region to protein factors during class switching.PML nuclear bodies and apoptosis.Daxx represses RelB target promoters via DNA methyltransferase recruitment and DNA hypermethylationDaxx and TCF4 interaction links to oral squamous cell carcinoma growth by promoting cell cycle progression via induction of cyclin D1 expression.Pax5 and linker histone H1 coordinate DNA methylation and histone modifications in the 3' regulatory region of the immunoglobulin heavy chain locus.The regulation of the B-cell gene expression programme by Pax5.Regulation of apoptosis by PML and the PML-NBs.B-lineage transcription factors and cooperating gene lesions required for leukemia development.Daxx is a transcriptional repressor of CCAAT/enhancer-binding protein betaProteasome-dependent degradation of Daxx by the viral E1B-55K protein in human adenovirus-infected cells.PAX5 is expressed in small-cell lung cancer and positively regulates c-Met transcription.Identification of Daxx interacting with p73, one of the p53 family, and its regulation of p53 activity by competitive interaction with PML4-Hydroxynonenal self-limits fas-mediated DISC-independent apoptosis by promoting export of Daxx from the nucleus to the cytosol and its binding to Fas.Human Daxx-mediated repression of human cytomegalovirus gene expression correlates with a repressive chromatin structure around the major immediate early promoter.Ets-1-dependent expression of vascular endothelial growth factor receptors is activated by latency-associated nuclear antigen of Kaposi's sarcoma-associated herpesvirus through interaction with Daxx.The transcriptional repressor hDaxx potentiates p53-dependent apoptosis.Tryptophan 621 and serine 667 residues of Daxx regulate its nuclear export during glucose deprivation.
P2860
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P248
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P2860
The interaction of Pax5 (BSAP) with Daxx can result in transcriptional activation in B cells
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2002 nî lūn-bûn
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2002 թուականի Մարտին հրատարակուած գիտական յօդուած
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2002 թվականի մարտին հրատարակված գիտական հոդված
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2002年の論文
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2002年論文
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2002年論文
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2002年論文
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The interaction of Pax5 (BSAP) ...... iptional activation in B cells
@ast
The interaction of Pax5 (BSAP) ...... iptional activation in B cells
@en
The interaction of Pax5 (BSAP) ...... iptional activation in B cells
@en-gb
The interaction of Pax5 (BSAP) ...... iptional activation in B cells
@nl
type
label
The interaction of Pax5 (BSAP) ...... iptional activation in B cells
@ast
The interaction of Pax5 (BSAP) ...... iptional activation in B cells
@en
The interaction of Pax5 (BSAP) ...... iptional activation in B cells
@en-gb
The interaction of Pax5 (BSAP) ...... iptional activation in B cells
@nl
prefLabel
The interaction of Pax5 (BSAP) ...... iptional activation in B cells
@ast
The interaction of Pax5 (BSAP) ...... iptional activation in B cells
@en
The interaction of Pax5 (BSAP) ...... iptional activation in B cells
@en-gb
The interaction of Pax5 (BSAP) ...... iptional activation in B cells
@nl
P2093
P2860
P921
P356
P1476
The interaction of Pax5 (BSAP) ...... iptional activation in B cells
@en
P2093
Alexander V Emelyanov
Barbara K Birshtein
Cecilia R Kovac
Manuel A Sepulveda
P2860
P304
P356
10.1074/JBC.M111763200
P407
P577
2002-03-29T00:00:00Z