Genome-independent hypoxic repression of estrogen receptor alpha in breast cancer cells
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2407
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Genome-independent hypoxic repression of estrogen receptor alpha in breast cancer cells ; volume:17 ; number:1 ; day:20 ; month:3 ; year:2017 ; pages:1-16 ; date:12.2017
BMC cancer ; 17, Heft 1 (20.3.2017), 1-16, 12.2017
- Schlagwort
-
Krebs
Onkologie
- Urheber
-
Padró, Mercè
- Beteiligte Personen und Organisationen
-
Louie, Raymond J.
Lananna, Brian V.
Krieg, Adam J.
Timmerman, Luika A.
Chan, Denise A.
SpringerLink (Online service)
- DOI
-
10.1186/s12885-017-3140-9
- URN
-
urn:nbn:de:1111-201704095429
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
- 14.08.2025, 10:59 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Padró, Mercè
- Louie, Raymond J.
- Lananna, Brian V.
- Krieg, Adam J.
- Timmerman, Luika A.
- Chan, Denise A.
- SpringerLink (Online service)
Ähnliche Objekte (12)
![Regulation of estrogen responsive genes by human estrogen receptor alpha (ERα) [(ER-Alpha)]](/assets/placeholder/searchResultMediaUnknown.png)
Regulation of estrogen responsive genes by human estrogen receptor alpha (ERα) [(ER-Alpha)]
Transcriptional repression of estrogen receptor alpha by YAP reveals the Hippo pathway as therapeutic target for ER+ breast cancer
Biomolekulare Interaktionsanalyse des humanen Estrogen Rezeptors alpha
Estrogen independent gene expression defines clinically relevant subgroups of estrogen receptor positive breast cancer
Autocrine regulation of cell proliferation by estrogen receptor-alpha in estrogen receptor-alpha-positive breast cancer cell lines
Polymorphisms in the estrogen receptor alpha gene (ESR1), daily cycling estrogen and mammographic density phenotypes
Characterization of estrogen receptor α [alpha] in mouse osteoblasts
Alternative splicing of estrogen receptor alpha in hepatocellular carcinoma
Characterization of estrogen receptor α [alpha] in mouse osteoblasts
Ligands specify estrogen receptor alpha nuclear localization and degradation
Decursin and decursinol angelate inhibit estrogen-stimulated and estrogen-independent growth and survival of breast cancer cells
Misoprostol regulates Bnip3 repression and alternative splicing to control cellular calcium homeostasis during hypoxic stress
Regulation of estrogen responsive genes by human estrogen receptor alpha (ERα) [(ER-Alpha)]
Transcriptional repression of estrogen receptor alpha by YAP reveals the Hippo pathway as therapeutic target for ER+ breast cancer
Biomolekulare Interaktionsanalyse des humanen Estrogen Rezeptors alpha
Estrogen independent gene expression defines clinically relevant subgroups of estrogen receptor positive breast cancer
Autocrine regulation of cell proliferation by estrogen receptor-alpha in estrogen receptor-alpha-positive breast cancer cell lines
Polymorphisms in the estrogen receptor alpha gene (ESR1), daily cycling estrogen and mammographic density phenotypes
Characterization of estrogen receptor α [alpha] in mouse osteoblasts
Alternative splicing of estrogen receptor alpha in hepatocellular carcinoma
Characterization of estrogen receptor α [alpha] in mouse osteoblasts
Ligands specify estrogen receptor alpha nuclear localization and degradation
Decursin and decursinol angelate inhibit estrogen-stimulated and estrogen-independent growth and survival of breast cancer cells
Misoprostol regulates Bnip3 repression and alternative splicing to control cellular calcium homeostasis during hypoxic stress
Regulation of estrogen responsive genes by human estrogen receptor alpha (ERα) [(ER-Alpha)]
Transcriptional repression of estrogen receptor alpha by YAP reveals the Hippo pathway as therapeutic target for ER+ breast cancer
Biomolekulare Interaktionsanalyse des humanen Estrogen Rezeptors alpha
Estrogen independent gene expression defines clinically relevant subgroups of estrogen receptor positive breast cancer
Autocrine regulation of cell proliferation by estrogen receptor-alpha in estrogen receptor-alpha-positive breast cancer cell lines
Polymorphisms in the estrogen receptor alpha gene (ESR1), daily cycling estrogen and mammographic density phenotypes
Characterization of estrogen receptor α [alpha] in mouse osteoblasts
Alternative splicing of estrogen receptor alpha in hepatocellular carcinoma
Characterization of estrogen receptor α [alpha] in mouse osteoblasts
Ligands specify estrogen receptor alpha nuclear localization and degradation
Decursin and decursinol angelate inhibit estrogen-stimulated and estrogen-independent growth and survival of breast cancer cells