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Combinatorial Chemistry & High Throughput Screening
|
June 22, 2006
Analysing the output from primary screening
Dawn Nowlin, Patrick Bingham, Andrew Berridge, et al.
Chemical Biology & Drug Design
|
August 8, 2009
Structural and biophysical characterization of XIAP BIR3 G306E mutant: insights in protein dynamics and application for fragment-based drug design
Cathy D Moore, Haihong Wu, Ben Bolaños, et al.
Protein Science : a Publication of the Protein Society
|
October 4, 2012
Identification of Cys255 in HIF-1α as a novel site for development of covalent inhibitors of HIF-1α/ARNT PasB domain protein-protein interaction
Rosa Cardoso, Robert Love, Carol L Nilsson, et al.
Nature Chemical Biology
|
May 30, 2017
Targeting S-adenosylmethionine biosynthesis with a novel allosteric inhibitor of Mat2A
Casey L Quinlan, Stephen E Kaiser, Ben Bolaños, et al.
Journal of Medicinal Chemistry
|
October 31, 2009
Azaindole hydroxamic acids are potent HIV-1 integrase inhibitors
Michael B Plewe, Scott L Butler, Klaus R Dress, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
Combinatorial Chemistry & High Throughput Screening
|
June 22, 2006
Analysing the output from primary screening
Dawn Nowlin, Patrick Bingham, Andrew Berridge, et al.
Chemical Biology & Drug Design
|
August 8, 2009
Structural and biophysical characterization of XIAP BIR3 G306E mutant: insights in protein dynamics and application for fragment-based drug design
Cathy D Moore, Haihong Wu, Ben Bolaños, et al.
Protein Science : a Publication of the Protein Society
|
October 4, 2012
Identification of Cys255 in HIF-1α as a novel site for development of covalent inhibitors of HIF-1α/ARNT PasB domain protein-protein interaction
Rosa Cardoso, Robert Love, Carol L Nilsson, et al.
Nature Chemical Biology
|
May 30, 2017
Targeting S-adenosylmethionine biosynthesis with a novel allosteric inhibitor of Mat2A
Casey L Quinlan, Stephen E Kaiser, Ben Bolaños, et al.
Journal of Medicinal Chemistry
|
October 31, 2009
Azaindole hydroxamic acids are potent HIV-1 integrase inhibitors
Michael B Plewe, Scott L Butler, Klaus R Dress, et al.
Page
of 1