118 results on '"Treiber, Daniel"'
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2. 9. “BIGNESS” & EURALILLE (1989–1998): I KNEW I WAS IN TROUBLE BUT I THOUGHT I WAS IN HELL
3. An Optimal Mg2+ Concentration for Kinetic Folding of the Tetrahymena Ribozyme
4. Kinetic Intermediates Trapped by Native Interactions in RNA Folding
5. Management of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Onboard a U.S. Navy Hospital Ship Amid a Global Omicron Surge
6. Management of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Onboard a U.S. Navy Hospital Ship Amid a Global Omicron Surge
7. Cisplatin-DNA Adducts are Molecular Decoys for the Ribosomal RNA Transcription Factor hUBF (Human Upstream Binding Factor)
8. Forschungsbericht 2012
9. Utilizing comprehensive and mini-kinome panels to optimize the selectivity of quinoline inhibitors for cyclin G associated kinase (GAK)
10. Abstract 6408: E3scan™ ligand binding assay platform for targeted protein degradation and PROTAC discovery
11. The Kinase Chemogenomic Set (KCGS): An open science resource for kinase vulnerability identification
12. Norman Foster
13. Frank Lloyd Wright
14. A CCHC metal‐binding domain in Nanos is essential for translational regulation
15. Ins and Outs of Kinase DFG Motifs
16. [21] Kinetic oligonucleotide hybridization for monitoring kinetic folding of large RNAs
17. The Kinase Chemogenomic Set (KCGS): An open science resource for kinase vulnerability identification
18. Utilizing comprehensive and mini-kinome panels to optimize the selectivity of quinoline inhibitors for cyclin G associated kinase (GAK)
19. Donated chemical probes for open science
20. Author response: Donated chemical probes for open science
21. Progress towards a public chemogenomic set for protein kinases and a call for contributions
22. Progress towards a public chemogenomic set for protein kinases and a call for contributions
23. Identification of a Chemical Probe for Family VIII Bromodomains through Optimization of a Fragment Hit
24. Les Sept Lampes et l’architecture organique de Frank Lloyd Wright
25. Novel series of pyrrolotriazine analogs as highly potent pan-Aurora kinase inhibitors
26. Abstract 5387: Dual kinase/bromodomain inhibitors for rationally designed polypharmacology
27. Erratum: Corrigendum: Dual kinase-bromodomain inhibitors for rationally designed polypharmacology
28. Dual kinase-bromodomain inhibitors for rationally designed polypharmacology
29. Arylcarboxyamino-substituted diaryl ureas as potent and selective FLT3 inhibitors
30. Abstract 4238: BROMOscan - a high throughput, quantitative ligand binding platform identifies best-in-class bromodomain inhibitors from a screen of mature compounds targeting other protein classes.
31. Abstract 4538: A novel assay platform for the detection of kinase-inhibitor binding in intact mammalian cells.
32. Discovery of AC710, a Globally Selective Inhibitor of Platelet-Derived Growth Factor Receptor-Family Kinases
33. Abstract LB-390: High throughput, quantitative ligand binding assays for human bromodomains
34. Discovery of Highly Potent and Selective Pan-Aurora Kinase Inhibitors with Enhanced in Vivo Antitumor Therapeutic Index
35. Comprehensive analysis of kinase inhibitor selectivity
36. Activation State-Dependent Binding of Small Molecule Kinase Inhibitors: Structural Insights from Biochemistry
37. A quantitative analysis of kinase inhibitor selectivity
38. Structure of the Kinase Domain of an Imatinib-Resistant Abl Mutant in Complex with the Aurora Kinase Inhibitor VX-680
39. Response to Molecule–kinase interaction map
40. Reply to BIRB-796 is not an effective ABL(T315I) inhibitor
41. A small molecule–kinase interaction map for clinical kinase inhibitors
42. Beyond kinetic traps in RNA folding
43. Concerted kinetic folding of a multidomain ribozyme with a disrupted loop-receptor interaction
44. An optimal Mg 2+ concentration for kinetic folding of the Tetrahymena ribozyme
45. Exposing the kinetic traps in RNA folding
46. Fast folding mutants of the Tetrahymena group I ribozyme reveal a rugged folding energy landscape 1 1Edited by D. Draper
47. A simple method for preparing pools of synthetic oligonucleotides with random point deletions
48. An ultraviolet light-damaged DNA recognition protein absent in xeroderma pigmentosum group E cells binds selectively to pyrimidine (6–4) pyrimidone photoproducts
49. Characterization of a DNA damage-recognition protein from mammalian cells that binds specifically to intrastrand d(GpG) and d(ApG) DNA adducts of the anticancer drug cisplatin
50. Fast folding mutants of the Tetrahymenagroup I ribozyme reveal a rugged folding energy landscape11Edited by D. Draper
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