Muscle hypertrophy in hypoxia with inflammation is controlled by bromodomain and extra-terminal domain proteins
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2045-2322
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
-
Muscle hypertrophy in hypoxia with inflammation is controlled by bromodomain and extra-terminal domain proteins ; volume:7 ; number:1 ; day:21 ; month:9 ; year:2017 ; pages:1-11 ; date:12.2017
Scientific reports ; 7, Heft 1 (21.9.2017), 1-11, 12.2017
- Creator
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Chabert, Clovis
Khochbin, Saadi
Rousseaux, Sophie
Furze, Rebecca
Smithers, Nicholas
Prinjha, Rab
Schlattner, Uwe
Pison, Christophe
Dubouchaud, Hervé
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41598-017-12112-0
- URN
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urn:nbn:de:101:1-2019081000313317749937
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
- 15.08.2025, 7:21 AM CEST
Data provider
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Chabert, Clovis
- Khochbin, Saadi
- Rousseaux, Sophie
- Furze, Rebecca
- Smithers, Nicholas
- Prinjha, Rab
- Schlattner, Uwe
- Pison, Christophe
- Dubouchaud, Hervé
- SpringerLink (Online service)
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Bromodomain and extra-terminal (BET) proteins target Moloney murine leukemia virus integration to transcription start sites
Rapamycin attenuates hypoxia-induced pulmonary vascular remodeling and right ventricular hypertrophy in mice
Discovery of a PCAF bromodomain chemical probe
Discovery of a PCAF Bromodomain Chemical Probe
Hepatitis C virus NS4B carboxy terminal domain is a membrane binding domain
Cotranslational folding of HemK C-terminal domain
Bromodomain-containing factor GTE4 regulates Arabidopsis immune response
Functional analysis of the N-terminal domain of SPA1
Bromodomain and extra-terminal domain (BET) proteins regulate melanocyte differentiation
Discovery of Benzo (d) imidazole‐6‐sulfonamides as Bromodomain and Extra‐Terminal Domain (BET) Inhibitors with Selectivity for the First Bromodomain
Mechanisms of resistance to inhibitors of bromodomain and extra-terminal domain (BET) proteins in MYC-driven medulloblastoma
Selectively Binding a Bromodomain
Bromodomain and extra-terminal (BET) proteins target Moloney murine leukemia virus integration to transcription start sites
Rapamycin attenuates hypoxia-induced pulmonary vascular remodeling and right ventricular hypertrophy in mice
Discovery of a PCAF bromodomain chemical probe
Discovery of a PCAF Bromodomain Chemical Probe
Hepatitis C virus NS4B carboxy terminal domain is a membrane binding domain
Cotranslational folding of HemK C-terminal domain
Bromodomain-containing factor GTE4 regulates Arabidopsis immune response
Functional analysis of the N-terminal domain of SPA1
Bromodomain and extra-terminal domain (BET) proteins regulate melanocyte differentiation
Discovery of Benzo (d) imidazole‐6‐sulfonamides as Bromodomain and Extra‐Terminal Domain (BET) Inhibitors with Selectivity for the First Bromodomain
Mechanisms of resistance to inhibitors of bromodomain and extra-terminal domain (BET) proteins in MYC-driven medulloblastoma
Selectively Binding a Bromodomain
Bromodomain and extra-terminal (BET) proteins target Moloney murine leukemia virus integration to transcription start sites
Rapamycin attenuates hypoxia-induced pulmonary vascular remodeling and right ventricular hypertrophy in mice
Discovery of a PCAF bromodomain chemical probe
Discovery of a PCAF Bromodomain Chemical Probe
Hepatitis C virus NS4B carboxy terminal domain is a membrane binding domain
Cotranslational folding of HemK C-terminal domain
Bromodomain-containing factor GTE4 regulates Arabidopsis immune response