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Finding new components of the target of rapamycin (TOR) signaling network through chemical genetics and proteome chips 원문보기

Proceedings of the National Academy of Sciences of the United States of America, v.101 no.47, 2004년, pp.16594 - 16599  

Huang, Jing (Howard Hughes Medical Institute, Harvard Institute of Chemistry and Cell Biology, and Departments of Chemistry and Chemical Biology and Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138) ,  Zhu, Heng (Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT 06520) ,  Haggarty, Stephen J. (and Department of Molecular and Medical Pharmacology, University of California, Los Angeles, CA 90095) ,  Spring, David R. (Howard Hughes Medical Institute, Harvard Institute of Chemistry and Cell Biology, and Departments of Chemistry and Chemical Biology and Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138) ,  Hwang, Heejun (Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT 06520) ,  Jin, Fulai (and Department of Molecular and Medical Pharmacology, University of California, Los Angeles, CA 90095) ,  Snyder, Michael (Howard Hughes Medical Institute, Harvard Institute of Chemistry and Cell Biology, and Departments of Chemistry and Chemical Biology and Molecular and Cellular Biology, Harvar) ,  Schreiber, Stuart L.

Abstract AI-Helper 아이콘AI-Helper

The TOR (target of rapamycin) proteins play important roles in nutrient signaling in eukaryotic cells. Rapamycin treatment induces a state reminiscent of the nutrient starvation response, often resulting in growth inhibition. Using a chemical genetic modifier screen, we identified two classes of sm...

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