• 14 Hits
  • 検索条件 : 絞込み (MeSH = Protein Kinase Inhibitors* / pharmacology)
生物種 リソース名 タイトル
ヒト・動物細胞 EoL-1 cell(RCB0641) Mislocalisation of FLT3-ITD receptor contributes to MV4-11 leukaemia cell resistance to antibody-drug conjugate.
ヒト・動物細胞 HuCCT1(RCB1960) , TFK-1(RCB2537) Fadraciclib, a CDK2/CDK9 inhibitor, shows efficacy in biliary tract cancer and synergistic potential with olaparib and JQ1 based on MCL1 expression.
ヒト・動物細胞 Ba/F3(RCB0805) Zidesamtinib Selective Targeting of Diverse ROS1 Drug-Resistant Mutations.
ヒト・動物細胞 PC-12(RCB0009) Inhibitory Effects of Vandetanib on Catecholamine Synthesis in Rat Pheochromocytoma PC12 Cells.
ヒト・動物細胞 Ba/F3(RCB0805) Preclinical characterization of TGRX-678, a brain-penetrant allosteric inhibitor of BCR::ABL1.
ヒト・動物細胞 Ba/F3(RCB4476) Efficacy of Conventional and Novel Tyrosine Kinase Inhibitors for Uncommon EGFR Mutations-An In Vitro Study.
ヒト・動物細胞 HeLa , COS-7(RCB0539) Protein kinase C (PKC) inhibitor Calphostin C activates PKC in a light-dependent manner at high concentrations via the production of singlet oxygen.
遺伝子材料 pTcf7wtluc (RDB02968) Basroparib overcomes acquired resistance to MEK inhibitors by inhibiting Wnt-mediated cancer stemness in KRAS-mutated colorectal cancer.
実験動物マウス RBRC09532 Jun N-Terminal Kinase Inhibitor Suppresses CASK Deficiency-Induced Cerebellar Granular Cell Death in MICPCH Syndrome Model Mice.
ヒト・動物細胞 Huh7(RCB1366) , Huh6(RCB1367) Dual Inhibition of CDK4/6 and XPO1 Induces Senescence With Acquired Vulnerability to CRBN-Based PROTAC Drugs.
ヒト・動物細胞 CHO-K1(RCB0285) , HeLa((RCB0007) , A431(RCB0202) , Ba/F3(RCB4476) Single molecule tracking based drug screening.
ヒト・動物細胞 NIH3T3 MEK inhibitors and DA-Raf, a dominant-negative antagonist of the Ras-ERK pathway, prevent the migration and invasion of KRAS-mutant cancer cells.
ヒト・動物細胞 EBC-1(RCB1965) PAI-1 mediates acquired resistance to MET-targeted therapy in non-small cell lung cancer.
ヒト・動物細胞 PC-9(RCB4455) Inhibition of EGFR and MEK surmounts entrectinib resistance in a brain metastasis model of NTRK1-rearranged tumor cells.