Ted Powers, Ph.D.
Affiliations: | Molecular and Cellular Biology | University of California, Davis, Davis, CA |
Area:
cell growth, TOR pathwayWebsite:
http://biosci3.ucdavis.edu/FacultyAndResearch/FacultyProfile.aspx?FacultyID=265Google:
"Ted Powers"Children
Sign in to add traineeIvanka M. Dilova | grad student | 2005 | UC Davis |
Ching-Yi Chen | grad student | 2006 | UC Davis |
Andrew William Hill | grad student | 2010 | UC Davis |
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Publications
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Tsverov J, Yegorov K, Powers T. (2022) Identification of defined structural elements within TOR2 kinase required for TOR complex 2 assembly and function in . Molecular Biology of the Cell. 33: ar44 |
Hill A, Niles B, Cuyegkeng A, et al. (2018) Redesigning TOR Kinase to Explore the Structural Basis for TORC1 and TORC2 Assembly. Biomolecules. 8 |
Carmona-Gutierrez D, Bauer MA, Zimmermann A, et al. (2018) Guidelines and recommendations on yeast cell death nomenclature. Microbial Cell (Graz, Austria). 5: 4-31 |
Vlahakis A, Lopez Muniozguren N, Powers T. (2017) Stress-response transcription factors Msn2 and Msn4 couple TORC2-Ypk1 signaling and mitochondrial respiration to ATG8 gene expression and autophagy. Autophagy. 1-9 |
Murley A, Yamada J, Niles BJ, et al. (2017) Sterol transporters at membrane contact sites regulate TORC1 and TORC2 signaling. The Journal of Cell Biology. 216: 2679-2689 |
Vlahakis A, Lopez Muniozguren N, Powers T. (2017) Mitochondrial respiration links TOR Complex 2 signaling to calcium regulation and autophagy. Autophagy. 0 |
Vlahakis A, Lopez Muniozguren N, Powers T. (2016) Calcium channel regulator Mid1 links TORC2-mediated changes in mitochondrial respiration to autophagy. The Journal of Cell Biology |
Stauffer B, Powers T. (2016) Target of rapamycin signaling mediates vacuolar fragmentation. Current Genetics |
Klionsky DJ, Abdelmohsen K, Abe A, et al. (2016) Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition). Autophagy. 12: 1-222 |
Stauffer B, Powers T. (2015) Target of rapamycin signaling mediates vacuolar fission caused by endoplasmic reticulum stress in S. cerevisiae. Molecular Biology of the Cell |