Rapamycin-modulated transcription defines the subset of nutrient-sensitive signaling pathways directly controlled by the Tor proteins
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference35 articles.
1. Targets for Cell Cycle Arrest by the Immunosuppressant Rapamycin in Yeast
2. TOR controls translation initiation and early G1 progression in yeast.
3. Target of rapamycin proteins and their kinase activities are required for meiosis
4. Tor, a Phosphatidylinositol Kinase Homologue, Controls Autophagy in Yeast
5. Rapamycin Induces the G 0 Program of Transcriptional Repression in Yeast by Interfering with the TOR Signaling Pathway
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