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Proceedings of the National Academy of Sciences of the United States of America|February 20, 2004
Gene transfer in the evolution of parasite nucleotide biosynthesisBoris Striepen, Andrea J P Pruijssers, Jinling Huang, et al.
Journal of Medicinal Chemistry|July 24, 2009
Triazole inhibitors of Cryptosporidium parvum inosine 5'-monophosphate dehydrogenaseSushil K Maurya, Deviprasad R Gollapalli, Shivapriya Kirubakaran, et al.
Journal of Medicinal Chemistry|September 7, 2012
Selective and potent urea inhibitors of cryptosporidium parvum inosine 5'-monophosphate dehydrogenaseSuresh Kumar Gorla, Mandapati Kavitha, Minjia Zhang, et al.
Plos Biology|August 30, 2008
An enzymatic atavist revealed in dual pathways for water activationDonghong Min, Helen R Josephine, Hongzhi Li, et al.
Bioorganic & Medicinal Chemistry Letters|January 18, 2013
Phthalazinone inhibitors of inosine-5'-monophosphate dehydrogenase from Cryptosporidium parvumCorey R Johnson, Suresh Kumar Gorla, Mandapati Kavitha, et al.
Bioorganic & Medicinal Chemistry Letters|December 12, 2018
Diarylcarbonates are a new class of deubiquitinating enzyme inhibitorMarcus J C Long, Ann P Lawson, Rick Baggio, et al.
The Biochemical Journal|September 16, 2011
Adaptive evolution of drug targets in producer and non-producer organismsBjarne G Hansen, Xin E Sun, Hans J Genee, et al.
Oncotarget|September 9, 2017
Identification of deubiquitinase targets of isothiocyanates using SILAC-assisted quantitative mass spectrometryAnn P Lawson, Daniel W Bak, D Alexander Shannon, et al.
Bioorganic & Medicinal Chemistry Letters|February 8, 2012
Structure-activity relationship study of selective benzimidazole-based inhibitors of Cryptosporidium parvum IMPDHSivapriya Kirubakaran, Suresh Kumar Gorla, Lisa Sharling, et al.
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