In vivo complex formation of PU.1 with HDAC1 associated with PU.1-mediated transcriptional repression. - Wikidata - awgldk - TriplyDB

In vivo complex formation of PU.1 with HDAC1 associated with PU.1-mediated transcriptional repression.

In vivo complex formation of PU.1 with HDAC1 associated with PU.1-mediated transcriptional repression.

http://www.wikidata.org/entity/Q40775802

about

Cooperative interaction between ETS1 and GFI1 transcription factors in the repression of Bax gene expression Metallothionein-1 isoforms and vimentin are direct PU.1 downstream target genes in leukemia cells Functional cross-antagonism between transcription factors FLI-1 and EKLF Extensive remodeling of DC function by rapid maturation-induced transcriptional silencing.Role of hypoxia in the regulation of periovulatory EDN2 expression in the mouse.RUNX1 regulates corepressor interactions of PU.1.PU.1 Suppresses Th2 Cytokine Expression via Silencing of GATA3 Transcription in Dendritic Cells.ETS transcription factors: possible targets for cancer therapy.PU.1 and pRB interact and cooperate to repress GATA-1 and block erythroid differentiation Transcriptional activators, repressors, and epigenetic modifiers controlling hematopoietic stem cell development.Digging deep into "dirty" drugs - modulation of the methylation machinery.Spi-B inhibits human plasma cell differentiation by repressing BLIMP1 and XBP-1 expression.Overlapping CRE and E box motifs in the enhancer sequences of the bovine leukemia virus 5' long terminal repeat are critical for basal and acetylation-dependent transcriptional activity of the viral promoter: implications for viral latency.Epstein-Barr virus EBNA-3C is targeted to and regulates expression from the bidirectional LMP-1/2B promoter.Dynamic protein associations define two phases of IL-1beta transcriptional activation.Genetic determination of the role of PU.1 in macrophage gene expression The HTLV-I p30 interferes with TLR4 signaling and modulates the release of pro- and anti-inflammatory cytokines from human macrophages.Deacetylase inhibitors and the viral transactivator TaxBLV synergistically activate bovine leukemia virus gene expression via a cAMP-responsive element- and cAMP-responsive element-binding protein-dependent mechanism.Transcriptional regulation of mouse mu opioid receptor gene by PU.1.The interaction of HTLV-1 Tax with HDAC1 negatively regulates the viral gene expression.Combinatorial control of DNase I-hypersensitive site formation and erasure by immunoglobulin heavy chain enhancer-binding proteins.Up regulation of GW112 Gene by NF kappaB promotes an antiapoptotic property in gastric cancer cells.

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P2860

In vivo complex formation of PU.1 with HDAC1 associated with PU.1-mediated transcriptional repression.

http://www.wikidata.org/entity/Q40775802

description

2001 nî lūn-bûn

@nan

2001年の論文

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2001年学术文章

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2001年学术文章

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2001年学术文章

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2001年学术文章

@zh-my

2001年学术文章

@zh-sg

2001年學術文章

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2001年學術文章

@zh

2001年學術文章

@zh-hant

name

In vivo complex formation of P ...... ed transcriptional repression.

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type

label

In vivo complex formation of P ...... ed transcriptional repression.

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In vivo complex formation of P ...... ed transcriptional repression.

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In vivo complex formation of P ...... ed transcriptional repression.

@en

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Kihara-Negishi F

http://www.w3.org/2001/XMLSchema#string

Oikawa T

http://www.w3.org/2001/XMLSchema#string

Sakurai T

http://www.w3.org/2001/XMLSchema#string

Suzuki M

http://www.w3.org/2001/XMLSchema#string

Tamura T

http://www.w3.org/2001/XMLSchema#string

Yamada T

http://www.w3.org/2001/XMLSchema#string

Yamamoto H

http://www.w3.org/2001/XMLSchema#string

P2860

Histone deacetylases specifically down-regulate p53-dependent gene activation

Two domains of p53 interact with the TATA-binding protein, and the adenovirus 13S E1A protein disrupts the association, relieving p53-mediated transcriptional repression

The activation domain of transcription factor PU.1 binds the retinoblastoma (RB) protein and the transcription factor TFIID in vitro: RB shows sequence similarity to TFIID and TFIIB

Direct interaction of hematopoietic transcription factors PU.1 and GATA-1: functional antagonism in erythroid cells

The tau 4 activation domain of the thyroid hormone receptor is required for release of a putative corepressor(s) necessary for transcriptional silencing

Molecular mechanisms of myogenic coactivation by p300: direct interaction with the activation domain of MyoD and with the MADS box of MEF2C

Two contact regions between Stat1 and CBP/p300 in interferon gamma signaling

A CBP integrator complex mediates transcriptional activation and AP-1 inhibition by nuclear receptors

The macrophage and B cell-specific transcription factor PU.1 is related to the ets oncogene

Physical and functional interactions between the transcription factor PU.1 and the coactivator CBP

P2888

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6039-6047

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scholarly article

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10.1038/SJ.ONC.1204756

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42

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20

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2001-09-01T00:00:00Z

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11757368

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1005215820

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11593411

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