Identifying Phagocytic Receptors for Entamoeba Histolytica
Adam graduated from UVM in ’07 with degrees in Biochemistry and Biology. He joined the CMB program in ’09 after working in Dr. Karen Lounsbury’s lab for 2 years. His research focuses on identifying phagocytic receptors for Entamoeba histolytica, one of the leading causes of disenteric disease.
Sateriale A, Roy NH, Huston CD (2013) SNAP-tag technology optimized for use in Entamoeba histolytica. PLoS One 8(12): e83997.
Koenig A, Sateriale A, Budd RC, Huber SA, Buskiewicz IA (2014) The role of sex differences in autophagy in the heart during coxsackievirus b3-induced myocarditis. J Cardiovasc Transl Res 7(2): 182-91.
Sateriale A, Bessoff K, Sarkar IN, Huston CD (2014) Drug repurposing: mining protozoan proteomes for targets of known bioactive compounds. J Am Med Inform Assoc 21(2): 238-44.
Bessoff K, Sateriale A, Lee KK, Huston CD (2013) Drug repurposing screen reveals FDA-approved inhibitors of human HMG-CoA reductase and isoprenoid synthesis that block Cryptosporidium parvum growth. Antimicrob Agents Chemother 57(4): 1804-14.
Sateriale A, Vaithilingam A, Donnelly L, Miller P, Huston CD (2012) Feed-forward regulation of phagocytosis by Entamoeba histolytica. Infect Immun 80(12): 4456-62.
Teixeira JE, Sateriale A, Bessoff KE, Huston CD (2012) Control of Entamoeba histolytica adherence involves metallosurface protease 1, an M8 family surface metalloprotease with homology to leishmanolysin. Infect Immun 80(6): 2165-76.
Sateriale A, Huston CD (2011) A Sequential Model of Host Cell Killing and Phagocytosis by Entamoeba histolytica. J Parasitol Res 2011: 926706.
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