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Reproduction (Cambridge, England)|November 3, 2025
Inhibition of fatty acid amide hydrolase leads to uterine vascular defects and decreased fertility in pregnant ratsVanesa A Cañumil, Fernanda L de la Cruz Borthiry, Frida Scheffer, et al.
Bioorganic & Medicinal Chemistry Letters|February 8, 2006
Structure-guided identification of novel VEGFR-2 kinase inhibitors via solution phase parallel synthesisRabindranath Tripathy, Alyssa Reiboldt, Patricia A Messina, et al.
Optics Letters|January 16, 2019
Hong-Ou-Mandel interference between independent III-V on silicon waveguide integrated lasersC Agnesi, B Da Lio, D Cozzolino, et al.
Arthritis Research & Therapy|April 23, 2011
A highly selective, orally active inhibitor of Janus kinase 2, CEP-33779, ablates disease in two mouse models of rheumatoid arthritisKristine L Stump, Lily D Lu, Pawel Dobrzanski, et al.
Bioorganic & Medicinal Chemistry Letters|May 1, 2010
8-THP-DHI analogs as potent Type I dual TIE-2/VEGF-R2 receptor tyrosine kinase inhibitorsRobert L Hudkins, Allison L Zulli, Ted L Underiner, et al.
Bioorganic & Medicinal Chemistry Letters|March 1, 2008
Design and synthesis of dihydroindazolo[5,4-a]pyrrolo[3,4-c]carbazole oximes as potent dual inhibitors of TIE-2 and VEGF-R2 receptor tyrosine kinasesReddeppareddy Dandu, Allison L Zulli, Edward R Bacon, et al.
Journal of Medicinal Chemistry|January 13, 2015
Design, synthesis, and biological evaluation of sulfonyl acrylonitriles as novel inhibitors of cancer metastasis and spreadYi Shen, Craig A Zificsak, Jill E Shea, et al.
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