20 results on '"Fernández-Montalván, Amaury E."'
Search Results
2. Figure S2 from Inhibition of BUB1 Kinase by BAY 1816032 Sensitizes Tumor Cells toward Taxanes, ATR, and PARP Inhibitors In Vitro and In Vivo
3. Supplementary Figure Legends and Methods from Inhibition of BUB1 Kinase by BAY 1816032 Sensitizes Tumor Cells toward Taxanes, ATR, and PARP Inhibitors In Vitro and In Vivo
4. Characterization of 12 GnRH peptide agonists – a kinetic perspective
5. Discovery and Characterization of BAY 1214784, an Orally Available Spiroindoline Derivative Acting as a Potent and Selective Antagonist of the Human Gonadotropin-Releasing Hormone Receptor as Proven in a First-In-Human Study in Postmenopausal Women
6. Treating Cancer by Spindle Assembly Checkpoint Abrogation: Discovery of Two Clinical Candidates, BAY 1161909 and BAY 1217389, Targeting MPS1 Kinase
7. Characterization of the Menin-MLL Interaction as Therapeutic Cancer Target
8. Considerations for improved performance of competition association assays analysed with the Motulsky–Mahan's “kinetics of competitive binding” model
9. Inhibition of BUB1 Kinase by BAY 1816032 Sensitizes Tumor Cells toward Taxanes, ATR, and PARP Inhibitors In Vitro and In Vivo
10. Halogenaromatische π-Wechselwirkungen modulieren die Verweilzeit von Inhibitoren
11. Halogen-Aromatic π Interactions Modulate Inhibitor Residence Times
12. Isoform-Selective ATAD2 Chemical Probe with Novel Chemical Structure and Unusual Mode of Action
13. Abstract 287: BAY 1816032, a novel BUB1 kinase inhibitor with potent antitumor activity
14. Abstract 5084: Potent and isoform-selective ATAD2 bromodomain inhibitor with unprecedented chemical structure and mode of action
15. Abstract 160: High target binding affinity with long lasting cellular target engagement and high dose intermittent schedule of PI3K inhibitor copanlisib contribute to the potent anti-tumor activity and good safety profile
16. Abstract 980: BAY-299, a novel chemical probe for in-depth analysis of the function of the bromodomain proteins BRPF2 and TAF1
17. Benzoisoquinolinediones as Potent and Selective Inhibitors of BRPF2 and TAF1/TAF1L Bromodomains
18. ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication
19. Characterization of 12 GnRH peptide agonists - a kinetic perspective
20. ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.