BSAP can repress enhancer activity by targeting PU.1 function.
about
The interaction of Pax5 (BSAP) with Daxx can result in transcriptional activation in B cellsThe transcriptional repressor GFI-1 antagonizes PU.1 activity through protein-protein interactionThe third helix of the homeodomain of paired class homeodomain proteins acts as a recognition helix both for DNA and protein interactionsBSAP (Pax5)-importin alpha 1 (Rch1) interaction identifies a nuclear localization sequenceSuperactivation of Pax6-mediated transactivation from paired domain-binding sites by dna-independent recruitment of different homeodomain proteinsMaturation stage-specific regulation of megakaryopoiesis by pointed-domain Ets proteinsPredicting combinatorial binding of transcription factors to regulatory elements in the human genome by association rule miningLong-range interactions between three transcriptional enhancers, active Vkappa gene promoters, and a 3' boundary sequence spanning 46 kilobasesPU.1 is involved in the regulation of B lineage-associated and developmental stage-dependent expression of the germinal center-associated DNA primase GANP.Pax5 determines the identity of B cells from the beginning to the end of B-lymphopoiesis.The long winding road toward understanding the molecular mechanisms for B-cell suppression by 2,3,7,8-tetrachlorodibenzo-p-dioxinEvolution of hematopoiesis: Three members of the PU.1 transcription factor family in a cartilaginous fish, Raja eglanteria.Hematopoietic cytokines, transcription factors and lineage commitment.Epigenetic histone modifications do not control Igkappa locus contraction and intranuclear localization in cells with dual B cell-macrophage potential.B-Lymphoma cells with epigenetic silencing of Pax5 trans-differentiate into macrophages, but not other hematopoietic lineages.Regulation of activation and recombination of the murine Igkappa locus.B cell activator PAX5 promotes lymphomagenesis through stimulation of B cell receptor signaling.Oscillation between B-lymphoid and myeloid lineages in Myc-induced hematopoietic tumors following spontaneous silencing/reactivation of the EBF/Pax5 pathway.The regulation of the B-cell gene expression programme by Pax5.Highly cooperative recruitment of Ets-1 and release of autoinhibition by Pax5.Role of mir-15a/16-1 in early B cell development in a mouse model of chronic lymphocytic leukemia.B-lineage transcription factors and cooperating gene lesions required for leukemia development.E2A Antagonizes PU.1 Activity through Inhibition of DNA Binding.Epstein-Barr virus EBNA-3C is targeted to and regulates expression from the bidirectional LMP-1/2B promoter.YY1 controls immunoglobulin class switch recombination and nuclear activation-induced deaminase levels.A developmentally controlled competitive STAT5-PU.1 DNA binding mechanism regulates activity of the Ig κ E3' enhancer.Control of megakaryocyte-specific gene expression by GATA-1 and FOG-1: role of Ets transcription factorsA novel pax5-binding regulatory element in the igκ locus.Corecruitment of the Grg4 repressor by PU.1 is critical for Pax5-mediated repression of B-cell-specific genes.The mechanism of repression of the myeloid-specific c-fms gene by Pax5 during B lineage restrictionLoss of B cell identity correlates with loss of B cell-specific transcription factors in Hodgkin/Reed-Sternberg cells of classical Hodgkin lymphoma.Diversification of haematopoietic stem cells to specific lineages.
P2860
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P2860
BSAP can repress enhancer activity by targeting PU.1 function.
description
2000 nî lūn-bûn
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2000年の論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年论文
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name
BSAP can repress enhancer activity by targeting PU.1 function.
@ast
BSAP can repress enhancer activity by targeting PU.1 function.
@en
type
label
BSAP can repress enhancer activity by targeting PU.1 function.
@ast
BSAP can repress enhancer activity by targeting PU.1 function.
@en
prefLabel
BSAP can repress enhancer activity by targeting PU.1 function.
@ast
BSAP can repress enhancer activity by targeting PU.1 function.
@en
P2860
P1476
BSAP can repress enhancer activity by targeting PU.1 function.
@en
P2093
P2860
P304
P356
10.1128/MCB.20.6.1911-1922.2000
P407
P577
2000-03-01T00:00:00Z