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ACS Medicinal Chemistry Letters|June 6, 2014
Selective Inhibitors of Fibroblast Activation Protein (FAP) with a (4-Quinolinoyl)-glycyl-2-cyanopyrrolidine ScaffoldKoen Jansen, Leen Heirbaut, Jonathan D Cheng, et al.Biofabrication|July 1, 2017
Scaling-up of a HepaRG progenitor cell based bioartificial liver: optimization for clinical application and transportMartien van Wenum, Philipp Treskes, Chung-Yin Tang, et al.Frontiers in Immunology|June 15, 2018
GMP-Grade Manufacturing of T Cells Engineered to Express a Defined γδTCRTrudy Straetemans, Guido J J Kierkels, Ruud Doorn, et al.ACS Medicinal Chemistry Letters|July 14, 2026
Correction to "Novel Small Molecule-Derived, Highly Selective Substrates for Fibroblast Activation Protein (FAP)"An De Decker, Gwendolyn Vliegen, Dries Van Rompaey, et al.ACS Medicinal Chemistry Letters|August 16, 2019
Novel Small Molecule-Derived, Highly Selective Substrates for Fibroblast Activation Protein (FAP)An De Decker, Gwendolyn Vliegen, Dries Van Rompaey, et al.Journal of Medicinal Chemistry|March 25, 2024
Discovery of GLPG2737, a Potent Type 2 Corrector of CFTR for the Treatment of Cystic Fibrosis in Combination with a Potentiator and a Type 1 Co-correctorMathieu Pizzonero, Rhalid Akkari, Xavier Bock, et al.Journal of Medicinal Chemistry|September 28, 2021
Discovery and Optimization of Orally Bioavailable Phthalazone and Cinnolone Carboxylic Acid Derivatives as S1P2 Antagonists against Fibrotic DiseasesOscar Mammoliti, Koen Jansen, Sandy El Bkassiny, et al.Pageof 2