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The Journal of Steroid Biochemistry and Molecular Biology|September 12, 2017
CYP17A1-independent production of the neurosteroid-derived 5α-pregnan-3β,6α-diol-20-one in androgen-responsive prostate cancer cell lines under serum starvation and inhibition by AbirateroneAntonio G Gomes de Mello Martins, Giuseppe Allegretta, Gerhard Unteregger, et al.The Gerontologist|May 3, 2018
Impact of Intervention to Improve Nursing Home Resident-Staff Interactions and EngagementChristine W Hartmann, Whitney L Mills, Camilla B Pimentel, et al.Implementation Science Communications|June 23, 2021
Virtual external implementation facilitation: successful methods for remotely engaging groups in quality improvementChristine W Hartmann, Ryann L Engle, Camilla B Pimentel, et al.The EMBO Journal|November 18, 2006
Allosteric activation of the protein kinase PDK1 with low molecular weight compoundsMatthias Engel, Valerie Hindie, Laura A Lopez-Garcia, et al.The Gerontologist|May 13, 2017
Development of a New Tool for Systematic Observation of Nursing Home Resident and Staff Engagement and RelationshipA Lynn Snow, M Lindsey Jacobs, Jennifer A Palmer, et al.Lung Cancer (Amsterdam, Netherlands)|January 19, 2016
Blood group antigen A type 3 expression is a favorable prognostic factor in advanced NSCLCL H Schmidt, A Kuemmel, C Schliemann, et al.Journal of Medicinal Chemistry|January 16, 2019
Targeted Endocrine Therapy: Design, Synthesis, and Proof-of-Principle of 17β-Hydroxysteroid Dehydrogenase Type 2 Inhibitors in Bone Fracture HealingAhmed S Abdelsamie, Steven Herath, Yannik Biskupek, et al.Journal of Medicinal Chemistry|April 1, 2021
From Celecoxib to a Novel Class of Phosphodiesterase 5 Inhibitors: Trisubstituted Pyrazolines as Novel Phosphodiesterase 5 Inhibitors with Extremely High Potency and Phosphodiesterase Isozyme SelectivityMohammad Abdel-Halim, Sara Sigler, Nora A S Racheed, et al.Journal of Medicinal Chemistry|July 26, 2019
Design, Synthesis, and Biological Characterization of Orally Active 17β-Hydroxysteroid Dehydrogenase Type 2 Inhibitors Targeting the Prevention of OsteoporosisAhmed S Abdelsamie, Mohamed Salah, Lorenz Siebenbürger, et al.Bioorganic & Medicinal Chemistry|December 7, 2007
Synthesis, biological evaluation and molecular modelling studies of methyleneimidazole substituted biaryls as inhibitors of human 17alpha-hydroxylase-17,20-lyase (CYP17). Part I: Heterocyclic modifications of the core structureCarsten Jagusch, Matthias Negri, Ulrike E Hille, et al.Pageof 59