Transcriptional regulation of the stress response by mTOR
Author:
Affiliation:
1. Department of Experimental and Health Sciences, Universitat Pompeu Fabra, Barcelona 08003, Spain.
2. Centre for Genomic Regulation and Universitat Pompeu Fabra, Barcelona 08003, Spain.
Abstract
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference187 articles.
1. mTOR Controls Cell Cycle Progression through Its Cell Growth Effectors S6K1 and 4E-BP1/Eukaryotic Translation Initiation Factor 4E
2. mTOR Interacts with Raptor to Form a Nutrient-Sensitive Complex that Signals to the Cell Growth Machinery
3. Raptor, a Binding Partner of Target of Rapamycin (TOR), Mediates TOR Action
4. Rictor, a Novel Binding Partner of mTOR, Defines a Rapamycin-Insensitive and Raptor-Independent Pathway that Regulates the Cytoskeleton
5. Identification of Sin1 as an essential TORC2 component required for complex formation and kinase activity
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