23 results on '"Diehl, Wade"'
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2. Supplemental Methods from Spectrum and Degree of CDK Drug Interactions Predicts Clinical Performance
3. Supplemental Tables S1-S9 from Spectrum and Degree of CDK Drug Interactions Predicts Clinical Performance
4. Data from Spectrum and Degree of CDK Drug Interactions Predicts Clinical Performance
5. KIT Kinase Mutants Show Unique Mechanisms of Drug Resistance to Imatinib and Sunitinib in Gastrointestinal Stromal Tumor Patients
6. Development of hepatitis C virus chimeric replicons for identifying broad spectrum NS3 protease inhibitors
7. Abstract 330: Engineering electrophile-sensitive kinase mutants to accelerate oncology target validation
8. KIT kinase mutants show unique mechanisms of drug resistance to imatinib and sunitinib gastrointestinal stromal tumor patients
9. Discovery of PF-06873600, a CDK2/4/6 Inhibitor for the Treatment of Cancer
10. Function of activation loop tyrosine phosphorylation in the mechanism of c-Kit auto-activation and its implication in sunitinib resistance
11. Drug binding and resistance mechanism of KIT tyrosine kinase revealed by hydrogen/deuterium exchange FTICR mass spectrometry
12. The Crystal Structure of the RNA-Dependent RNA Polymerase from Human Rhinovirus: A Dual Function Target for Common Cold Antiviral Therapy
13. Characterizing the effects of the juxtamembrane domain on vascular endothelial growth factor receptor-2 enzymatic activity, autophosphorylation, and inhibition by axitinib
14. SAH derived potent and selective EZH2 inhibitors
15. Autocrine regulation of interleukin-8 production in human monocytes
16. Correction to Design and Synthesis of Pyridone-Containing 3,4-Dihydroisoquinoline-1(2H)-ones as a Novel Class of Enhancer of Zeste Homolog 2 (EZH2) Inhibitors
17. Spectrum and Degree of CDK Drug Interactions Predicts Clinical Performance
18. Design and Synthesis of Pyridone-Containing 3,4-Dihydroisoquinoline-1(2H)-ones as a Novel Class of Enhancer of Zeste Homolog 2 (EZH2) Inhibitors
19. Polycomb repressive complex 2 structure with inhibitor reveals a mechanism of activation and drug resistance
20. Design and Synthesis of Pyridone-Containing 3,4-Dihydroisoquinoline-1(2H)-ones as a Novel Class of Enhancer of Zeste Homolog 2 (EZH2) Inhibitors.
21. Characterizing the Effects of the Juxtamembrane Domain on Vascular Endothelial Growth Factor Receptor-2 Enzymatic Activity, Autophosphorylation, and Inhibition by Axitinib
22. Crystallographic Identification of a Noncompetitive Inhibitor Binding Site on the Hepatitis C Virus NS5B RNA Polymerase Enzyme
23. The Crystal Structure of the RNA-Dependent RNA Polymerase from Human Rhinovirus A Dual Function Target for Common Cold Antiviral Therapy
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