Small molecule inhibitor targeting the Hsp70-Bim protein–protein interaction in estrogen receptor-positive breast cancer overcomes tamoxifen resistance
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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Small molecule inhibitor targeting the Hsp70-Bim protein–protein interaction in estrogen receptor-positive breast cancer overcomes tamoxifen resistance ; volume:26 ; number:1 ; day:26 ; month:2 ; year:2024 ; pages:1-13 ; date:12.2024
Breast cancer research ; 26, Heft 1 (26.2.2024), 1-13, 12.2024
- Creator
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Song, Ting
Zhang, Hong
Zhao, Qicheng
Hu, Zhiyuan
Wang, Ziqian
Song, Yang
Zhang, Zhichao
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s13058-024-01790-0
- URN
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urn:nbn:de:101:1-2405021256510.167661495616
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:50 AM CEST
Data provider
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Associated
- Song, Ting
- Zhang, Hong
- Zhao, Qicheng
- Hu, Zhiyuan
- Wang, Ziqian
- Song, Yang
- Zhang, Zhichao
- SpringerLink (Online service)
Other Objects (12)
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Mammalian enabled protein enhances tamoxifen sensitivity of the hormone receptor-positive breast cancer patients by suppressing the AKT signaling pathway
Multivalent protein–protein interactions are pivotal regulators of eukaryotic Hsp70 complexes
Protein Kinase A-induced tamoxifen resistance is mediated by anchoring protein AKAP13
Stimulation of TLR4 by recombinant HSP70 requires structural integrity of the HSP70 protein itself
Crucial HSP70 co-chaperone complex unlocks metazoan protein disaggregation
Transfection of Heat Shock Protein 70 kDa (HSP70)
Raptor localization predicts prognosis and tamoxifen response in estrogen receptor-positive breast cancer
Characterization of a the Plasmodium falciparum Hsp70-Hsp90 organising protein
LONP1 and mtHSP70 cooperate to promote mitochondrial protein folding
Predicting prognosis using molecular profiling in estrogen receptor-positive breast cancer treated with tamoxifen
Nogo-B receptor increases the resistance to tamoxifen in estrogen receptor-positive breast cancer cells
Hsp70 at the membrane: driving protein translocation
Mammalian enabled protein enhances tamoxifen sensitivity of the hormone receptor-positive breast cancer patients by suppressing the AKT signaling pathway
Multivalent protein–protein interactions are pivotal regulators of eukaryotic Hsp70 complexes
Protein Kinase A-induced tamoxifen resistance is mediated by anchoring protein AKAP13
Stimulation of TLR4 by recombinant HSP70 requires structural integrity of the HSP70 protein itself
Crucial HSP70 co-chaperone complex unlocks metazoan protein disaggregation
Transfection of Heat Shock Protein 70 kDa (HSP70)
Raptor localization predicts prognosis and tamoxifen response in estrogen receptor-positive breast cancer
Characterization of a the Plasmodium falciparum Hsp70-Hsp90 organising protein
LONP1 and mtHSP70 cooperate to promote mitochondrial protein folding
Predicting prognosis using molecular profiling in estrogen receptor-positive breast cancer treated with tamoxifen
Nogo-B receptor increases the resistance to tamoxifen in estrogen receptor-positive breast cancer cells
Hsp70 at the membrane: driving protein translocation
Mammalian enabled protein enhances tamoxifen sensitivity of the hormone receptor-positive breast cancer patients by suppressing the AKT signaling pathway
Multivalent protein–protein interactions are pivotal regulators of eukaryotic Hsp70 complexes
Protein Kinase A-induced tamoxifen resistance is mediated by anchoring protein AKAP13
Stimulation of TLR4 by recombinant HSP70 requires structural integrity of the HSP70 protein itself
Crucial HSP70 co-chaperone complex unlocks metazoan protein disaggregation
Transfection of Heat Shock Protein 70 kDa (HSP70)
Raptor localization predicts prognosis and tamoxifen response in estrogen receptor-positive breast cancer
Characterization of a the Plasmodium falciparum Hsp70-Hsp90 organising protein
LONP1 and mtHSP70 cooperate to promote mitochondrial protein folding
Predicting prognosis using molecular profiling in estrogen receptor-positive breast cancer treated with tamoxifen