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    顯示項目51-60 / 147. (共15頁)
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    日期題名關聯
    2015-01 Identification of ligand efficient, fragment-like hits from an HTS library: Structure-based virtual screening and docking investigations of 2H- and 3H-pyrazolo tautomers for Aurora kinase A selectivity Journal of Computer-Aided Molecular Design. 2015 Jan;29(1):89-100.
    2014-12 BPR-3P0128 inhibits RNA-dependent RNA polymerase elongation and VPg uridylylation activities of Enterovirus 71 Antiviral Research. 2014 Dec;112:18-25.
    2014-10 Small-molecule EGFR tyrosine kinase inhibitors for the treatment of cancer Expert Opinion on Investigational Drugs. 2014 Oct;23(10):1333-1348.
    2014-08 CDKN1A-mediated responsiveness of MLL-AF4-positive acute lymphoblastic leukemia to Aurora kinase-A inhibitors International Journal of Cancer. 2014 Aug;135(3):751-762.
    2014-08 Ligand efficiency based approach for efficient virtual screening of compound libraries European Journal of Medicinal Chemistry. 2014 Aug;83:226-235.
    2014-07 Anaplastic lymphoma kinase (ALK) inhibitors: A review of design and discovery MedChemComm. 2014 Jul;5(9):1266-1279.
    2014-05 Facile identification of dual FLT3-Aurora A inhibitors: A computer-guided drug design approach ChemMedChem. 2014 May;9(5):953-961.
    2014-05 Cover Picture: Facile identification of dual FLT3–aurora a inhibitors: A computer-guided drug design approach (ChemMedChem 5/2014) ChemMedChem. 2014 May;9(5):861.
    2013-09-22 A novel Aurora-A inhibitor, BPR1K0609S1, sensitizes colorectal tumor cells to 5-fluorofracil (5-FU) treatment [Erratum:International Journal of Biological Sciences. 2013 Apr 29;9(4):403-411] International Journal of Biological Sciences. 2013 Sep 22;9(9):947.
    2013-07-25 Pronounced induction of endoplasmic reticulum stress and tumor suppression by surfactant-free poly(lactic-co-glycolic acid) nanoparticles via modulation of the PI3K signaling pathway International Journal of Nanomedicine. 2013 Jul 25;2013(8):2689-2707.

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