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Use of QSAR Global Models and Molecular Docking for Developing New Inhibitors of C-SRC Tyrosine Kinase
Are Janus Kinase Inhibitors Superior Over Classic Biologic Agents in RA Patients?
BioMed Research International
Immunology
Molecular Biology
Biochemistry
Microbiology
Medicine
Genetics
Synthetic Studies on Selective Type 4 Phosphodiesterase (PDE 4) Inhibitors. 1. Structure–Activity Relationships and Pharmacological Evaluation of 1,8-Naphthyridin-2(1h)-One Derivatives
Chemical and Pharmaceutical Bulletin
Medicine
Drug Discovery
Chemistry
Structure-Function Analysis of Ribonucleotide Bypass by B Family DNA Replicases
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Pan-SRC Family Kinase Inhibitors Replace Sox2 During the Direct Reprogramming of Somatic Cells
Angewandte Chemie - International Edition
Catalysis
Chemistry
Discovery of Conformationally Restricted Human Glutaminyl Cyclase Inhibitors as Potent Anti-Alzheimers Agents by Structure-Based Design
Synthesis of New Pyrrolo[1,2-A]quinoxaline Derivatives as Potential Inhibitors of Akt Kinase
Journal of Enzyme Inhibition and Medicinal Chemistry
Medicine
Drug Discovery
Pharmacology
Knockdown of Cyclin-Dependent Kinase Inhibitors Induces Cardiomyocyte Re-Entry in the Cell Cycle
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Crystal Structure of Thymidylate Kinase fromSaccharomyces Cerevisiaewith Substrate Bound
Acta Crystallographica Section A Foundations of Crystallography
Drosophila Cancer Models to Identify Inhibitors That Block an Optimized Combination of Kinase Targets
Science-Business eXchange
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