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Seminars in Oncology|August 15, 1998
Gene therapy for non-small cell lung cancer: a preliminary report of a phase I trial of adenoviral p53 gene replacementJ A Roth, S G Swisher, J A Merritt, et al.Journal of Molecular Biology|January 15, 2010
The crystal structure and activity of a putative trypanosomal nucleoside phosphorylase reveal it to be a homodimeric uridine phosphorylaseEric T Larson, Devaraja G Mudeppa, J Robert Gillespie, et al.Journal of Structural Biology|March 30, 2010
Prediction of protein crystallization outcome using a hybrid methodFrank H Zucker, Christine Stewart, Jaclyn dela Rosa, et al.Cancer Causes & Control : CCC|February 17, 2017
Pre-diagnosis insulin-like growth factor-I and risk of epithelial invasive ovarian cancer by histological subtypes: A collaborative re-analysis from the Ovarian Cancer Cohort ConsortiumJennifer Ose, Helena Schock, Elizabeth M Poole, et al.The Journal of Clinical Investigation|May 9, 2012
Transmission of malaria to mosquitoes blocked by bumped kinase inhibitorsKayode K Ojo, Claudia Pfander, Natascha R Mueller, et al.Nature Structural & Molecular Biology|May 4, 2010
Toxoplasma gondii calcium-dependent protein kinase 1 is a target for selective kinase inhibitorsKayode K Ojo, Eric T Larson, Katelyn R Keyloun, et al.European Journal of Medicinal Chemistry|February 18, 2014
Development of potent and selective Plasmodium falciparum calcium-dependent protein kinase 4 (PfCDPK4) inhibitors that block the transmission of malaria to mosquitoesRama Subba Rao Vidadala, Kayode K Ojo, Steven M Johnson, et al.Current Topics in Medicinal Chemistry|November 26, 2009
Fragment-based cocktail crystallography by the medical structural genomics of pathogenic protozoa consortiumChristophe L M J Verlinde, Erkang Fan, Sayaka Shibata, et al.Proteins|December 14, 2005
Crystal structure of glyceraldehyde-3-phosphate dehydrogenase from Plasmodium falciparum at 2.25 A resolution reveals intriguing extra electron density in the active siteMark A Robien, Jürgen Bosch, Frederick S Buckner, et al.ACS Medicinal Chemistry Letters|February 5, 2014
Potent and selective inhibitors of CDPK1 from T. gondii and C. parvum based on a 5-aminopyrazole-4-carboxamide scaffoldZhongsheng Zhang, Kayode K Ojo, Ramasubbarao Vidadala, et al.Pageof 58