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Conservation Biology : the Journal of the Society for Conservation Biology|September 17, 2013
Multiple lineages of Avian malaria parasites (Plasmodium) in the Galapagos Islands and evidence for arrival via migratory birdsI I Levin, P Zwiers, S L Deem, et al.Cellular and Molecular Biology (Noisy-Le-Grand, France)|September 8, 2000
Targeting exposed RNA regions in crystals of the small ribosomal subunits at medium resolutionH Bartels, M Gluehmann, D Janell, et al.Acta Crystallographica. Section A, Foundations of Crystallography|December 22, 1998
Crystallographic studies on the ribosome, a large macromolecular assembly exhibiting severe nonisomorphism, extreme beam sensitivity and no internal symmetryA Yonath, J Harms, H A Hansen, et al.Bioorganic & Medicinal Chemistry Letters|January 1, 1999
Malonyl alpha-mercaptoketones and alpha-mercaptoalcohols, a new class of matrix metalloproteinase inhibitorsD A Campbell, X Y Xiao, D Harris, et al.Cell Stem Cell|January 16, 2025
Longitudinal single-cell profiles of lung regeneration after viral infection reveal persistent injury-associated cell statesTerren K Niethamer, Joseph D Planer, Michael P Morley, et al.Journal of Structural Biology|October 21, 1999
Metal compounds as tools for the construction and the interpretation of medium-resolution maps of ribosomal particlesS Weinstein, W Jahn, C Glotz, et al.Molecular Cancer Therapeutics|November 9, 2007
Discovery of lactoquinomycin and related pyranonaphthoquinones as potent and allosteric inhibitors of AKT/PKB: mechanistic involvement of AKT catalytic activation loop cysteinesLourdes Toral-Barza, Wei-Guo Zhang, Xinyi Huang, et al.Bioorganic & Medicinal Chemistry Letters|April 2, 2003
Synthesis and SAR of bicyclic heteroaryl hydroxamic acid MMP and TACE inhibitorsA Zask, Y Gu, J D Albright, et al.Journal of Medicinal Chemistry|March 25, 2009
Pyranonaphthoquinone lactones: a new class of AKT selective kinase inhibitors alkylate a regulatory loop cysteineEdward J Salaski, Girija Krishnamurthy, Wei-Dong Ding, et al.Journal of Medicinal Chemistry|May 30, 2003
Synthesis and structure-activity relationship of N-substituted 4-arylsulfonylpiperidine-4-hydroxamic acids as novel, orally active matrix metalloproteinase inhibitors for the treatment of osteoarthritisVenkatesan Aranapakam, Jamie M Davis, George T Grosu, et al.Pageof 30