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Journal of Medicinal Chemistry|December 23, 2017
In Silico Fragment-Based Design Identifies Subfamily B1 Metallo-β-lactamase InhibitorsRicky Cain, Jürgen Brem, David Zollman, et al.RSC Medicinal Chemistry|August 3, 2022
<i>De novo</i> design of type II topoisomerase inhibitors as potential antimicrobial agents targeting a novel binding regionKyle M Orritt, Lipeng Feng, Juliette F Newell, et al.Biomolecules|June 18, 2020
Bicyclic Boronates as Potent Inhibitors of AmpC, the Class C β-Lactamase from <i>Escherichia coli</i>Pauline A Lang, Anete Parkova, Thomas M Leissing, et al.Nature Chemical Biology|April 30, 2014
Cyclic dinucleotides bind the C-linker of HCN4 to control channel cAMP responsivenessMarco Lolicato, Annalisa Bucchi, Cristina Arrigoni, et al.The Journal of Antimicrobial Chemotherapy|September 24, 2010
Benzothioxalone derivatives as novel inhibitors of UDP-N-acetylglucosamine enolpyruvyl transferases (MurA and MurZ)Keith Miller, Colin J Dunsmore, Jennifer A Leeds, et al.Nature Genetics|May 27, 2008
Mutations in 15-hydroxyprostaglandin dehydrogenase cause primary hypertrophic osteoarthropathySandeep Uppal, Christine P Diggle, Ian M Carr, et al.Biochimica Et Biophysica Acta. General Subjects|February 11, 2019
Studies on the inhibition of AmpC and other β-lactamases by cyclic boronatesSamuel T Cahill, Jonathan M Tyrrell, Iva Hopkins Navratilova, et al.Blood|January 11, 2013
The activation peptide cleft exposed by thrombin cleavage of FXIII-A(2) contains a recognition site for the fibrinogen α chainKerrie A Smith, Richard J Pease, Craig A Avery, et al.Nature Communications|December 7, 2017
Inhibition of D-Ala:D-Ala ligase through a phosphorylated form of the antibiotic D-cycloserineSarah Batson, Cesira de Chiara, Vita Majce, et al.Cell Calcium|October 18, 2011
Pregnenolone sulphate-independent inhibition of TRPM3 channels by progesteroneYasser Majeed, Sarka Tumova, Ben L Green, et al.Pageof 8