David M. Hockenbery

Affiliations: 
University of Washington, Seattle, Seattle, WA 
Area:
Cell Biology, Molecular Biology
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"David Hockenbery"
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Publications

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Lindsay K, Brenner C, Hockenbery D, et al. (2019) CBMT-30. TARGETING NICOTINAMIDE ADENINE DINUCLEOTIDE BIOSYNTHESIS IN CNS TUMORS Neuro-Oncology. 21: vi39-vi39
Bluestein BM, Morrish F, Graham DJ, et al. (2018) Analysis of the Myc-induced pancreatic cell islet tumor microenvironment using imaging ToF-SIMS. Biointerphases. 13: 06D402
Nagana Gowda GA, Barding GA, Dai J, et al. (2018) A Metabolomics Study of BPTES Altered Metabolism in Human Breast Cancer Cell Lines. Frontiers in Molecular Biosciences. 5: 49
Davis RJ, Gönen M, Margineantu DH, et al. (2018) Pan-cancer transcriptional signatures predictive of oncogenic mutations reveal that Fbw7 regulates cancer cell oxidative metabolism. Proceedings of the National Academy of Sciences of the United States of America
Steinbach G, Hockenbery DM, Huls G, et al. (2017) Pilot study of lithium to restore intestinal barrier function in severe graft-versus-host disease. Plos One. 12: e0183284
Berger S, Procko E, Margineantu D, et al. (2016) Computationally designed high specificity inhibitors delineate the roles of BCL2 family proteins in cancer. Elife. 5
Iwata TN, Ramírez JA, Tsang M, et al. (2016) Conditional Disruption of Raptor Reveals an Essential Role for mTORC1 in B Cell Development, Survival, and Metabolism. Journal of Immunology (Baltimore, Md. : 1950)
Margineantu DH, Hockenbery DM. (2016) Mitochondrial functions in stem cells. Current Opinion in Genetics & Development. 38: 110-117
Aguilar E, Marin de Mas I, Zodda E, et al. (2016) Metabolic Reprogramming and Dependencies Associated with Epithelial Cancer Stem Cells Independent of the Epithelial-Mesenchymal Transition Program. Stem Cells (Dayton, Ohio). 34: 1163-76
Berger S, Procko E, Margineantu D, et al. (2016) Author response: Computationally designed high specificity inhibitors delineate the roles of BCL2 family proteins in cancer Elife
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