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Chemmedchem|July 22, 2014
Development of diaminoquinazoline histone lysine methyltransferase inhibitors as potent blood-stage antimalarial compoundsSandeep Sundriyal, Nicholas A Malmquist, Joachim Caron, et al.
Journal of Medicinal Chemistry|June 17, 2015
Original 2-(3-Alkoxy-1H-pyrazol-1-yl)azines Inhibitors of Human Dihydroorotate Dehydrogenase (DHODH)Marianne Lucas-Hourani, Hélène Munier-Lehmann, Farah El Mazouni, et al.
Molecular Microbiology|March 4, 2008
Characterization of Trypanosoma brucei dihydroorotate dehydrogenase as a possible drug target; structural, kinetic and RNAi studiesTracy L Arakaki, Frederick S Buckner, J Robert Gillespie, et al.
Nature|July 22, 2014
Exonuclease-mediated degradation of nascent RNA silences genes linked to severe malariaQingfeng Zhang, T Nicolai Siegel, Rafael M Martins, et al.
Nature Medicine|February 11, 2014
Persistence and activation of malaria hypnozoites in long-term primary hepatocyte culturesLaurent Dembélé, Jean-François Franetich, Audrey Lorthiois, et al.
Molecular and Biochemical Parasitology|March 28, 2006
Regulation of surface coat exchange by differentiating African trypanosomesAmy E Gruszynski, Frederick J van Deursen, Maria C Albareda, et al.
Antimicrobial Agents and Chemotherapy|November 26, 2014
Histone methyltransferase inhibitors are orally bioavailable, fast-acting molecules with activity against different species causing malaria in humansNicholas A Malmquist, Sandeep Sundriyal, Joachim Caron, et al.
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