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Experimental Biology and Medicine (Maywood, N.J.)|August 4, 2012
Sphingosine kinase isoforms as a therapeutic target in endocrine therapy resistant luminal and basal-A breast cancerJames W Antoon, Martin D White, Jennifer L Driver, et al.Experimental Biology and Medicine (Maywood, N.J.)|June 24, 2009
Sphingolipids as determinants of apoptosis and chemoresistance in the MCF-7 cell model systemWilliam D Meacham, James W Antoon, Matthew E Burow, et al.Cancer Chemotherapy and Pharmacology|February 16, 2010
Novel D: -erythro N-octanoyl sphingosine analogs as chemo- and endocrine-resistant breast cancer therapeuticsJames W Antoon, Jiawang Liu, Adharsh P Ponnapakkam, et al.Journal of Medicinal Chemistry|August 22, 2009
Design, synthesis, and biological activity of a family of novel ceramide analogues in chemoresistant breast cancer cellsJames W Antoon, Jiawang Liu, Matthew M Gestaut, et al.Molecular Cancer|November 20, 2010
Effects of human mesenchymal stem cells on ER-positive human breast carcinoma cells mediated through ER-SDF-1/CXCR4 crosstalkLyndsay V Rhodes, James W Antoon, Shannon E Muir, et al.Cancer Letters|February 4, 2017
Oncogenic signaling of MEK5-ERK5Van T Hoang, Thomas J Yan, Jane E Cavanaugh, et al.International Journal of Oncology|September 6, 2007
Epigallocatechin-3 gallate induces growth inhibition and apoptosis in human breast cancer cells through survivin suppressionYan Tang, Daniel Y Zhao, Steven Elliott, et al.The Journal of Pharmacology and Experimental Therapeutics|January 27, 2004
Novel ceramide analogs as potential chemotherapeutic agents in breast cancerAmanda P Struckhoff, Robert Bittman, Matthew E Burow, et al.Carcinogenesis|November 8, 2003
Mechanism of AP-1-mediated gene expression by select organochlorines through the p38 MAPK pathwayDaniel E Frigo, Yan Tang, Barbara S Beckman, et al.The Journal of Cell Biology|November 10, 2004
The ERBB4/HER4 receptor tyrosine kinase regulates gene expression by functioning as a STAT5A nuclear chaperoneChristopher C Williams, June G Allison, Gregory A Vidal, et al.Pageof 5