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Journal of the American Chemical Society|October 3, 2002
Substrate-based design of the first class of angiotensin-converting enzyme-related carboxypeptidase (ACE2) inhibitorsNatalie A Dales, Alexandra E Gould, James A Brown, et al.
Reproductive Toxicology (Elmsford, N.Y.)|December 17, 2008
Developmental toxicity in white leghorn chickens following in ovo exposure to perfluorooctane sulfonate (PFOS)Margie M Peden-Adams, Joyce E Stuckey, Kristen M Gaworecki, et al.
Journal of Cellular Physiology|August 12, 2020
SPARC is a key mediator of TGF-β-induced renal cancer metastasisJi-Ming Bao, Qiang Dang, Chun-Jung Lin, et al.
Bioorganic & Medicinal Chemistry Letters|April 29, 2006
Identification and characterization of 4-aryl-3,4-dihydropyrimidin-2(1H)-ones as inhibitors of the fatty acid transporter FATP4Christopher Blackburn, Bing Guan, James Brown, et al.
Journal of Medicinal Chemistry|April 28, 2006
Design, synthesis, and progress toward optimization of potent small molecule antagonists of CC chemokine receptor 8 (CCR8)Shomir Ghosh, Amy Elder, Jianping Guo, et al.
The Journal of Allergy and Clinical Immunology|February 9, 2025
Efficacy and safety of GR1802 in uncontrolled chronic rhinosinusitis with nasal polyps: Placebo-controlled phase 2 trialMing Zheng, Di Wu, Yingshi Piao, et al.
Journal of Medicinal Chemistry|February 3, 2007
Design, synthesis, and evaluation of naphthalene-sulfonamide antagonists of human CCR8Tracy J Jenkins, Bing Guan, Mingshi Dai, et al.
Bioorganic & Medicinal Chemistry Letters|December 20, 2022
Discovery of structural diverse reversible BTK inhibitors utilized to develop a novel in vivo CD69 and CD86 PK/PD mouse modelGeorge H Vandeveer, Robert M Arduini, Darren P Baker, et al.
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