Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
3R01CA053370-04S1
Application #
2095292
Study Section
Virology Study Section (VR)
Project Start
1994-01-01
Project End
1995-12-31
Budget Start
1994-01-01
Budget End
1994-12-31
Support Year
4
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Rutgers University
Department
Type
Organized Research Units
DUNS #
038633251
City
New Brunswick
State
NJ
Country
United States
Zip Code
08901
Kimmelman, Alec C; White, Eileen (2017) Autophagy and Tumor Metabolism. Cell Metab 25:1037-1043
White, Eileen (2016) Autophagy and p53. Cold Spring Harb Perspect Med 6:a026120
(2016) Women in Metabolism: Part IV. Cell Metab 24:767-770
White, Eileen (2015) The role for autophagy in cancer. J Clin Invest 125:42-6
Guo, Jessie Yanxiang; White, Eileen (2013) Autophagy is required for mitochondrial function, lipid metabolism, growth, and fate of KRAS(G12D)-driven lung tumors. Autophagy 9:1636-8
Mao, Lili; Tang, Yuefeng; Vaiphei, S Thangminlal et al. (2009) Production of membrane proteins for NMR studies using the condensed single protein (cSPP) production system. J Struct Funct Genomics 10:281-9
Sundararajan, Ramya; Chen, Guanghua; Mukherjee, Chandreyee et al. (2005) Caspase-dependent processing activates the proapoptotic activity of deleted in breast cancer-1 during tumor necrosis factor-alpha-mediated death signaling. Oncogene 24:4908-20
Schwerk, Christian; Prasad, Jayendra; Degenhardt, Kurt et al. (2003) ASAP, a novel protein complex involved in RNA processing and apoptosis. Mol Cell Biol 23:2981-90
Perez, Denise; White, Eileen (2003) E1A sensitizes cells to tumor necrosis factor alpha by downregulating c-FLIP S. J Virol 77:2651-62
Henry, Holly; Thomas, Anju; Shen, Yan et al. (2002) Regulation of the mitochondrial checkpoint in p53-mediated apoptosis confers resistance to cell death. Oncogene 21:748-60

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