Identification of attractive drug targets in neglected-disease pathogens using an in silico approach by Crowther, Gregory J, Shanmugam, Dhanasekaran, Carmona, Santiago J, Doyle, Maria A, Hertz-Fowler, Christiane, Berriman, Matthew, Nwaka, Solomon, Ralph, Stuart A, Roos, David S, Van Voorhis, Wesley C, Agüero, Fernán

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novel CDPK1 inhibitor—a potential treatment for cryptosporidiosis in calves? by Lendner, Matthias, Böttcher, Denny, Delling, Cora, Ojo, Kayode K, Van Voorhis, Wesley C, Daugschies, Arwid

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Bumped kinase inhibitor prohibits egression in Babesia bovis by Pedroni, Monica J., Vidadala, Rama Subba Rao, Choi, Ryan, Keyloun, Katelyn R., Reid, Molly C., Murphy, Ryan C., Barrett, Lynn K., Van Voorhis, Wesley C., Maly, Dustin J., Ojo, Kayode K., Lau, Audrey O.T.

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Integrated dataset of screening hits against multiple neglected disease pathogens by Nwaka, Solomon, Besson, Dominique, Ramirez, Bernadette, Maes, Louis, Matheeussen, An, Bickle, Quentin, Mansour, Nuha R, Yousif, Fouad, Townson, Simon, Gokool, Suzanne, Cho-Ngwa, Fidelis, Samje, Moses, Misra-Bhattacharya, Shailja, Murthy, P K, Fakorede, Foluke, Paris, Jean-Marc, Yeates, Clive, Ridley, Robert, Van Voorhis, Wesley C, Geary, Timothy

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Crystal structures of Plasmodium falciparum cytosolic tryptophanyl-tRNA synthetase and its potential as a target for structure-guided drug design by Koh, Cho Yeow, Kim, Jessica E., Napoli, Alberto J., Verlinde, Christophe L.M.J., Fan, Erkang, Buckner, Frederick S., Van Voorhis, Wesley C., Hol, Wim G.J.

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Crystal structure and putative substrate identification for the Entamoeba histolytica low molecular weight tyrosine phosphatase by Linford, Alicia S., Jiang, Nona M., Edwards, Thomas E., Sherman, Nicholas E., Van Voorhis, Wesley C., Stewart, Lance J., Myler, Peter J., Staker, Bart L., Petri, William A.

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The Role of Medical Structural Genomics in Discovering New Drugs for Infectious Diseases: e1000530 by Voorhis, Wesley CVan, Hol, Wim GJ, Myler, Peter J, Stewart, Lance J

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Cofactor-Independent Phosphoglycerate Mutase from Nematodes Has Limited Druggability, as Revealed by Two High-Throughput Screens: e2628 by Crowther, Gregory J, Booker, Michael L, He, Min, Li, Ting, Raverdy, Sylvine, Novelli, Jacopo F, He, Panqing, Dale, Natalie RG, Fife, Amy M, Jr, Robert HBarker, Kramer, Martin L, Voorhis, Wesley CVan, Carlow, Clotilde KS, Wang, Ming-Wei

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Structurally Simple Farnesyltransferase Inhibitors Arrest the Growth of Malaria Parasites by Glenn, Matthew P., Chang, Sung-Youn, Hucke, Oliver, Verlinde, Christophe L. M. J., Rivas, Kasey, Hornéy, Carrie, Yokoyama, Kohei, Buckner, Frederick S., Pendyala, Prakash R., Chakrabarti, Debopam, Gelb, Michael, Van Voorhis, Wesley C., Sebti, Saïd M., Hamilton, Andrew D.

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Trypanosoma brucei glycogen synthase kinase-3, a target for anti-trypanosomal drug development: a public-private partnership to identify novel leads by Oduor, Richard O, Ojo, Kayode K, Williams, Gareth P, Bertelli, Francois, Mills, James, Maes, Louis, Pryde, David C, Parkinson, Tanya, Van Voorhis, Wesley C, Holler, Tod P

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Safety and Comparability of Controlled Human Plasmodium falciparum Infection by Mosquito Bite in Malaria-Naive Subjects at a New Facility for Sporozoite Challenge: e109654 by Talley, Angela K, Healy, Sara A, Finney, Olivia C, Murphy, Sean C, Kublin, James, Salas, Carola J, Lundebjerg, Susan, Gilbert, Peter, Voorhis, Wesley CVan, Whisler, John

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