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Molecular Cancer Therapeutics|April 17, 2008
MGCD0103, a novel isotype-selective histone deacetylase inhibitor, has broad spectrum antitumor activity in vitro and in vivoMarielle Fournel, Claire Bonfils, Yu Hou, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 18, 2016
Plasmin Prevents Dystrophic Calcification After Muscle InjuryNicholas A Mignemi, Masato Yuasa, Courtney E Baker, et al.
Bioorganic & Medicinal Chemistry Letters|January 22, 2008
4-(Heteroarylaminomethyl)-N-(2-aminophenyl)-benzamides and their analogs as a novel class of histone deacetylase inhibitorsSylvie Fréchette, Silvana Leit, Soon Hyung Woo, et al.
Bioorganic & Medicinal Chemistry Letters|February 13, 2009
N-(3-fluoro-4-(2-arylthieno[3,2-b]pyridin-7-yloxy)phenyl)-2-oxo-3-phenylimidazolidine-1-carboxamides: a novel series of dual c-Met/VEGFR2 receptor tyrosine kinase inhibitorsStéphane Raeppel, Stephen Claridge, Oscar Saavedra, et al.
Bioorganic & Medicinal Chemistry Letters|October 27, 2009
N-(4-(6,7-Disubstituted-quinolin-4-yloxy)-3-fluorophenyl)-2-oxo-3-phenylimidazolidine-1-carboxamides: a novel series of dual c-Met/VEGFR2 receptor tyrosine kinase inhibitorsMichael Mannion, Stéphane Raeppel, Stephen Claridge, et al.
Nature|June 10, 2016
Image-based detection and targeting of therapy resistance in pancreatic adenocarcinomaRaymond G Fox, Nikki K Lytle, Dawn V Jaquish, et al.
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