Arginine and glutamate-rich 1 (ARGLU1) interacts with mediator subunit 1 (MED1) and is required for estrogen receptor-mediated gene transcription and breast cancer cell growth - Wikidata - wikimedia - TriplyDB

Arginine and glutamate-rich 1 (ARGLU1) interacts with mediator subunit 1 (MED1) and is required for estrogen receptor-mediated gene transcription and breast cancer cell growth

Arginine and glutamate-rich 1 (ARGLU1) interacts with mediator subunit 1 (MED1) and is required for estrogen receptor-mediated gene transcription and breast cancer cell growth

http://www.wikidata.org/entity/Q24634157

about

ERK oscillation-dependent gene expression patterns and deregulation by stress response The alphabet of intrinsic disorder: II. Various roles of glutamic acid in ordered and intrinsically disordered proteins.An Ultraconserved Element (UCE) controls homeostatic splicing of ARGLU1 mRNA.Cross-talk between HER2 and MED1 regulates tamoxifen resistance of human breast cancer cells.In vivo evolution of tumor-derived endothelial cells.Cohesin is required for activation of MYC by estradiol.N-3 poly-unsaturated fatty acids shift estrogen signaling to inhibit human breast cancer cell growth.Silencing MED1 sensitizes breast cancer cells to pure anti-estrogen fulvestrant in vitro and in vivo.The effects of dietary supplementation with Agaricales mushrooms and other medicinal fungi on breast cancer: evidence-based medicine Oncogene amplification in male breast cancer: analysis by multiplex ligation-dependent probe amplification Stem cell and neurogenic gene-expression profiles link prostate basal cells to aggressive prostate cancer.Par-4/THAP1 complex and Notch3 competitively regulated pre-mRNA splicing of CCAR1 and affected inversely the survival of T-cell acute lymphoblastic leukemia cells Posterior Contraction Rates of the Phylogenetic Indian Buffet Processes.A new role for FBP21 as regulator of Brr2 helicase activity.MiR-873 regulates ERα transcriptional activity and tamoxifen resistance via targeting CDK3 in breast cancer cells.Identification of novel candidate disease genes from de novo exonic copy number variants.Near UV-Visible electronic absorption originating from charged amino acids in a monomeric protein.Fractionation iCLIP detects persistent SR protein binding to conserved, retained introns in chromatin, nucleoplasm and cytoplasm.The mediator complex in genomic and non-genomic signaling in cancer.

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P2860

Arginine and glutamate-rich 1 (ARGLU1) interacts with mediator subunit 1 (MED1) and is required for estrogen receptor-mediated gene transcription and breast cancer cell growth

http://www.wikidata.org/entity/Q24634157

description

2011 nî lūn-bûn

@nan

2011 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի մայիսին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Arginine and glutamate-rich 1 ...... and breast cancer cell growth

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Arginine and glutamate-rich 1 ...... and breast cancer cell growth

@en

Arginine and glutamate-rich 1 ...... and breast cancer cell growth

@nl

type

label

Arginine and glutamate-rich 1 ...... and breast cancer cell growth

@ast

Arginine and glutamate-rich 1 ...... and breast cancer cell growth

@en

Arginine and glutamate-rich 1 ...... and breast cancer cell growth

@nl

prefLabel

Arginine and glutamate-rich 1 ...... and breast cancer cell growth

@ast

Arginine and glutamate-rich 1 ...... and breast cancer cell growth

@en

Arginine and glutamate-rich 1 ...... and breast cancer cell growth

@nl

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JBC.M110.206029

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Journal of Biological Chemistry

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Arginine and glutamate-rich 1 ...... and breast cancer cell growth

@en

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Dingxiao Zhang

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

Pingping Jiang

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

Qinqin Xu

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

Xiaoting Zhang

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

P2860

The TRAP/Mediator coactivator complex interacts directly with estrogen receptors alpha and beta through the TRAP220 subunit and directly enhances estrogen receptor function in vitro

A set of consensus mammalian mediator subunits identified by multidimensional protein identification technology

Activation of TRAP/mediator subunit TRAP220/Med1 is regulated by mitogen-activated protein kinase-dependent phosphorylation

Coordination of p300-mediated chromatin remodeling and TRAP/mediator function through coactivator PGC-1alpha

MED1/TRAP220 exists predominantly in a TRAP/ Mediator subpopulation enriched in RNA polymerase II and is required for ER-mediated transcription

The TRAP220 component of a thyroid hormone receptor- associated protein (TRAP) coactivator complex interacts directly with nuclear receptors in a ligand-dependent fashion

Ligand induction of a transcriptionally active thyroid hormone receptor coactivator complex

MED1 phosphorylation promotes its association with mediator: implications for nuclear receptor signaling

Requirement of TRAP/mediator for both activator-independent and activator-dependent transcription in conjunction with TFIID-associated TAF(II)s.

TFIID and human mediator coactivator complexes assemble cooperatively on promoter DNA

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17746-54

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scholarly article

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10.1074/JBC.M110.206029

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20

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