Genome-wide RNAi Screening Identifies Protein Modules Required for 40S Subunit Synthesis in Human Cells
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
-
Englisch
- Bibliographic citation
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In: Cell Reports ; 13 (2015), 12. - S. 2879-2891. - eISSN 2211-1247
- Classification
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Biowissenschaften, Biologie
- Event
-
Veröffentlichung
- (where)
-
Konstanz
- (who)
-
Bibliothek der Universität Konstanz
- (when)
-
2016
- Creator
-
Badertscher, Lukas
Wild, Thomas
Montellese, Christian
Alexander, Leila T.
Bammert, Lukas
Sarazova, Marie
Stebler, Michael
Csúcs, Gábor
Mayer, Thomas U.
Zamboni, Nicola
Zemp, Ivo
Horvath, Peter
Kutay, Ulrike
- URN
-
urn:nbn:de:bsz:352-0-318278
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 11:03 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Badertscher, Lukas
- Wild, Thomas
- Montellese, Christian
- Alexander, Leila T.
- Bammert, Lukas
- Sarazova, Marie
- Stebler, Michael
- Csúcs, Gábor
- Mayer, Thomas U.
- Zamboni, Nicola
- Zemp, Ivo
- Horvath, Peter
- Kutay, Ulrike
- Bibliothek der Universität Konstanz
Time of origin
- 2016
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In vivo RNAi screen identifies candidate signaling genes required for collective cell migration in Drosophila ovary
RNAi phenotype profiling of kinases identifies potential therapeutic targets in Ewing's sarcoma
An in vivo RNAi screen identifies evolutionary conserved Drosophila fat storage regulators
The RNA-binding domain of DCL3 is required for long-distance RNAi signaling
Synthetic lethal RNAi screening identifies sensitizing targets for gemcitabine therapy in pancreatic cancer
Affinity proteomics identifies novel functional modules related to adhesion GPCRs
Publisher Correction: The RNA-binding domain of DCL3 is required for long-distance RNAi signaling
Multi-scale geometric network analysis identifies melanoma immunotherapy response gene modules
Phosphorylation‐linked complex profiling identifies assemblies required for Hippo signal integration
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