31 results on '"Öster, Linda"'
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2. Discovery and optimization of cyclohexane-1,4-diamines as allosteric MALT1 inhibitors
3. Structure and biophysical characterization of the human full-length neurturin–GFRa2 complex: A role for heparan sulfate in signaling
4. A class of highly selective inhibitors bind to an active state of PI3Kγ
5. Discovery and Characterization of a Bicyclic Peptide (Bicycle) Binder to Thymic Stromal Lymphopoietin.
6. Successful generation of structural information for fragment-based drug discovery
7. Structural and functional characterization of a specific antidote for ticagrelor
8. Design of small molecule inhibitors of acetyl-CoA carboxylase 1 and 2 showing reduction of hepatic malonyl-CoA levels in vivo in obese Zucker rats
9. Discovery of AZD8154, a Dual PI3Kγδ Inhibitor for the Treatment of Asthma
10. Insights into Cephamycin Biosynthesis: the Crystal Structure of CmcI from Streptomyces clavuligerus
11. Fragment-Based Discovery of Novel Allosteric MEK1 Binders
12. Conformational Flexibility of the C Terminus with Implications for Substrate Binding and Catalysis Revealed in a New Crystal Form of Deacetoxycephalosporin C Synthase
13. Biophysical methods to aid protein crystallization in a pharmaceutical setting
14. Heme Ligation and Conformational Plasticity in the Isolatedc Domain of Cytochrome cd1 Nitrite Reductase
15. Discovery of triazole aminopyrazines as a highly potent and selective series of PI3Kδ inhibitors
16. Discovery of Highly Isoform Selective Orally Bioavailable Phosphoinositide 3-Kinase (PI3K)-γ Inhibitors
17. Design and Synthesis of Soluble and Cell-Permeable PI3Kδ Inhibitors for Long-Acting Inhaled Administration
18. Discovery of a novel pyrazole series of group X secreted phospholipase A2 inhibitor (sPLA2X) via fragment based virtual screening
19. FAM3B PANDER and FAM3C ILEI Represent a Distinct Class of Signaling Molecules with a Non-Cytokine-like Fold
20. Fragment Screening of Soluble Epoxide Hydrolase for Lead Generation—Structure‐Based Hit Evaluation and Chemistry Exploration
21. Identification and Optimization of Benzimidazole Sulfonamides as Orally Bioavailable Sphingosine 1-Phosphate Receptor 1 Antagonists with in Vivo Activity
22. Gränsdragning vid värdepappershandel : -beskattning av finansiella- och icke-finansiella företag
23. Structure-function studies of beta-lactam biosynthetic enzymes
24. A SPECIFIC ANTIDOTE FOR TICAGRELOR
25. Creating Novel Activated Factor XI Inhibitors through Fragment Based Lead Generation and Structure Aided Drug Design
26. Solutions for the storage and handling of SPINE standard pucks
27. Clavatadine A, A Natural Product with Selective Recognition and Irreversible Inhibition of Factor XIa
28. The structural basis of cephalosporin formation in a mononuclear ferrous enzyme
29. Heme Ligation and Conformational Plasticity in the Isolatedc Domain of Cytochrome cd 1 Nitrite Reductase
30. Expression, purification, crystallization and preliminary X-ray diffraction studies of the cmcI component of Streptomyces clavuligerus 7α-cephem-methoxylase.
31. Heme Ligation and Conformational Plasticity in the IsolatedcDomain of Cytochrome cd1Nitrite Reductase*
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