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Nature Communications|June 28, 2017
The structural and functional characterization of human RecQ4 reveals insights into its helicase mechanismSebastian Kaiser, Florian Sauer, Caroline KiskerStructure (London, England : 1993)|December 12, 2017
Structural Basis for the Recruitment of Ctf18-RFC to the ReplisomeDaniel B Grabarczyk, Sabrina Silkenat, Caroline KiskerJournal of Computer-Aided Molecular Design|November 15, 2011
Molecular dynamics of Mycobacterium tuberculosis KasA: implications for inhibitor and substrate binding and consequences for drug designBenjamin Schaefer, Caroline Kisker, Christoph A SotrifferCurrent Topics in Medicinal Chemistry|March 10, 2007
Development of modern InhA inhibitors to combat drug resistant strains of Mycobacterium tuberculosisPeter J Tonge, Caroline Kisker, Richard A SlaydenBiochemistry|May 3, 2016
Selectivity of Pyridone- and Diphenyl Ether-Based Inhibitors for the Yersinia pestis FabV Enoyl-ACP ReductaseCarla Neckles, Annica Pschibul, Cheng-Tsung Lai, et al.The EMBO Journal|April 2, 2004
Lesion (in)tolerance reveals insights into DNA replication fidelityEva Freisinger, Arthur P Grollman, Holly Miller, et al.The Journal of Biological Chemistry|May 22, 2012
Raf kinase inhibitor protein (RKIP) dimer formation controls its target switch from Raf1 to G protein-coupled receptor kinase (GRK) 2Katharina Deiss, Caroline Kisker, Martin J Lohse, et al.Journal of Molecular Biology|June 6, 2003
Crystallographic characterization of an exocyclic DNA adduct: 3,N4-etheno-2'-deoxycytidine in the dodecamer 5'-CGCGAATTepsilonCGCG-3'Eva Freisinger, Andrea Fernandes, Arthur P Grollman, et al.The Journal of Biological Chemistry|September 18, 2009
Bax1 is a novel endonuclease: implications for archaeal nucleotide excision repairHeide M Roth, Ingrid Tessmer, Bennett Van Houten, et al.Science Signaling|January 28, 2010
Molecular basis of the death-associated protein kinase-calcium/calmodulin regulator complexIñaki de Diego, Jochen Kuper, Neda Bakalova, et al.Pageof 13