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Journal of Animal Science|June 6, 2012
Effects of diet source and vaccination for porcine circovirustype 2 and Mycoplasma hyopneumoniae on nursery pig performanceM L Potter, E M Kane, J R Bergstrom, et al.Leukemia & Lymphoma|July 7, 2020
Incidence, clinical presentation, and outcomes of Pneumocystis pneumonia when utilizing Polymerase Chain Reaction-based diagnosis in patients with Hodgkin lymphomaJason N Barreto, Carrie A Thompson, Patrick M Wieruszewski, et al.Chemmedchem|September 26, 2008
Synthesis of aromatase inhibitors and dual aromatase steroid sulfatase inhibitors by linking an arylsulfamate motif to 4-(4H-1,2,4-triazol-4-ylamino)benzonitrile: SAR, crystal structures, in vitro and in vivo activitiesChristian Bubert, L W Lawrence Woo, Oliver B Sutcliffe, et al.Journal of Thoracic Disease|October 29, 2025
Survival of patients with node-negative lung cancer and chest wall invasionAnupama Singh, Ashley L Deeb, Camille Mathey-Andrews, et al.Scientific Reports|May 21, 2016
A Small Molecule Inhibitor of PDK1/PLCγ1 Interaction Blocks Breast and Melanoma Cancer Cell InvasionClaudio Raimondi, Veronique Calleja, Riccardo Ferro, et al.Cancer|December 11, 2024
The 2021 US Preventive Services Task Force lung cancer screening eligibility criteria disproportionately exclude younger Black patients with lung cancerAlexandra L Potter, Sangkavi Kuhan, Priyanka Senthil, et al.ACS Medicinal Chemistry Letters|March 19, 2020
Regioisomeric Family of Novel Fluorescent Substrates for SHIP2Gaye White, Christopher Prior, Stephen J Mills, et al.Biochemical and Biophysical Research Communications|March 30, 2004
2-difluoromethyloestrone 3-O-sulphamate, a highly potent steroid sulphatase inhibitorJulie E Reed, L W Lawrence Woo, James J Robinson, et al.The Biochemical Journal|September 30, 2004
Crystal structure of human carbonic anhydrase II at 1.95 A resolution in complex with 667-coumate, a novel anti-cancer agentMatthew D Lloyd, Richard L Pederick, Ramanathan Natesh, et al.Chemmedchem|May 21, 2010
Discovery of adamantyl ethanone derivatives as potent 11beta-hydroxysteroid dehydrogenase type 1 (11beta-HSD1) inhibitorsXiangdong Su, Fabienne Pradaux-Caggiano, Mark P Thomas, et al.Pageof 69