Targeting BIG3-PHB2 interaction to overcome tamoxifen resistance in breast cancer cells. - Wikidata - awgldk - TriplyDB

Targeting BIG3-PHB2 interaction to overcome tamoxifen resistance in breast cancer cells.

Targeting BIG3-PHB2 interaction to overcome tamoxifen resistance in breast cancer cells.

http://www.wikidata.org/entity/Q37217695

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WDR5 Expression Is Prognostic of Breast Cancer Outcome.Stapled BIG3 helical peptide ERAP potentiates anti-tumour activity for breast cancer therapeutics.Brefeldin A-inhibited guanine nucleotide-exchange protein 3 (BIG3) is predicted to interact with its partner through an ARM-type α-helical structure A-kinase anchoring protein BIG3 coordinates oestrogen signalling in breast cancer cells.Early growth response 4 is involved in cell proliferation of small cell lung cancer through transcriptional activation of its downstream genes Xanthohumol suppresses oestrogen-signalling in breast cancer through the inhibition of BIG3-PHB2 interactions.BIG3 Inhibits the Estrogen-Dependent Nuclear Translocation of PHB2 via Multiple Karyopherin-Alpha Proteins in Breast Cancer Cells.Therapeutic advances in BIG3-PHB2 inhibition targeting the crosstalk between estrogen and growth factors in breast cancer Flaxseed and its components differentially affect estrogen targets in pre-neoplastic hen ovaries Minireview: The Link Between ERα Corepressors and Histone Deacetylases in Tamoxifen Resistance in Breast Cancer.In vitro Antiproliferative and Apoptosis Inducing Effect of Allium atroviolaceum Bulb Extract on Breast, Cervical, and Liver Cancer Cells.Significance of prohibitin domain family in tumorigenesis and its implication in cancer diagnosis and treatment.

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Targeting BIG3-PHB2 interaction to overcome tamoxifen resistance in breast cancer cells.

http://www.wikidata.org/entity/Q37217695

description

article científic

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article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on January 2013

@en

vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Targeting BIG3-PHB2 interaction to overcome tamoxifen resistance in breast cancer cells.

@en

Targeting BIG3-PHB2 interaction to overcome tamoxifen resistance in breast cancer cells.

@nl

type

label

Targeting BIG3-PHB2 interaction to overcome tamoxifen resistance in breast cancer cells.

@en

Targeting BIG3-PHB2 interaction to overcome tamoxifen resistance in breast cancer cells.

@nl

prefLabel

Targeting BIG3-PHB2 interaction to overcome tamoxifen resistance in breast cancer cells.

@en

Targeting BIG3-PHB2 interaction to overcome tamoxifen resistance in breast cancer cells.

@nl

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Nature Communications

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Targeting BIG3-PHB2 interaction to overcome tamoxifen resistance in breast cancer cells.

@en

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Eiichi Mizohata

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

Masato Komatsu

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

Miki Akiyama

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

Mitsunori Sasa

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Rui Yamaguchi

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Seiya Imoto

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Taisuke Matsuo

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Tetsuro Yoshimaru

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

Toyomasa Katagiri

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

Tsuyoshi Inoue

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

P2860

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Estrogen receptor alpha rapidly activates the IGF-1 receptor pathway

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Structure of the Cand1-Cul1-Roc1 complex reveals regulatory mechanisms for the assembly of the multisubunit cullin-dependent ubiquitin ligases

pp90rsk1 regulates estrogen receptor-mediated transcription through phosphorylation of Ser-167

Activation of apoptosis in vivo by a hydrocarbon-stapled BH3 helix.

Direct inhibition of the NOTCH transcription factor complex

In vivo activation of the p53 pathway by small-molecule antagonists of MDM2

The PSIPRED protein structure prediction server

Activation of estrogen receptor alpha by S118 phosphorylation involves a ligand-dependent interaction with TFIIH and participation of CDK7

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2443

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scholarly article

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10.1038/NCOMMS3443

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4

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2013-01-01T00:00:00Z

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256837134

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1008503019

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24051437

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3791465

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