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1. Functional Role and Therapeutic Potential of the Pim-1 Kinase in Colon Carcinoma

2. Inhibition of the SR protein-phosphorylating CLK kinases of Plasmodium falciparum impairs blood stage replication and malaria transmission.

3. PIM serine/threonine kinases in the pathogenesis and therapy of hematologic malignancies and solid cancers

5. Climate Capitalists

6. Discovery of High-Affinity Small-Molecule Binders of the Epigenetic Reader YEATS4

10. Corporate Discount Rates

11. Disaggregated Economic Accounts

12. A Chemical Probe for Tudor Domain Protein Spindlin1 to Investigate Chromatin Function

13. Fragment-based discovery of a chemical probe for the PWWP1 domain of NSD3

14. Alterations on growth and cell organization of Giardia intestinalis trophozoites after treatment with KH-TFMDI, a novel class III histone deacetylase inhibitor

15. A chemical biology toolbox to study protein methyltransferases and epigenetic signaling

16. Are Bigger Banks Better? Firm-Level Evidence from Germany

17. Circulating levels of proprotein convertase subtilisin/kexin type 9 (PCSK9) are associated with monocyte subsets in patients with stable coronary artery disease

18. Assays to Characterize the Cellular Pharmacology of a Chemical Probe

19. Deletion of the deISGylating enzyme USP18 enhances tumour cell antigenicity and radiosensitivity

20. Deliberately losing control of C-H activation processes in the design of small-molecule-fragment arrays targeting peroxisomal metabolism

21. Quantifying CDK inhibitor selectivity in live cells

22. Deep analysis of the USP18-dependent ISGylome and proteome unveils important roles for USP18 in tumour cell antigenicity and radiosensitivity

23. Quantifying Target Occupancy of Small Molecules Within Living Cells

24. Demonstration of the utility of DOS-derived fragment libraries for rapid hit derivatisation in a multidirectional fashion

26. Entdeckung einer chemischen Sonde für MLLT1/3-YEATS-Domänen

27. Nilotinib-induced vasculopathy: identification of vascular endothelial cells as a primary target site

28. Lapatinib potentiates cytotoxicity of YM155 in neuroblastoma via inhibition of the ABCB1 efflux transporter

29. Comprehensive Survey of CDK Inhibitor Selectivity in Live Cells with Energy Transfer Probes

30. Re-Evaluating the Mechanism of Action of α,β-Unsaturated Carbonyl DUB Inhibitors B-AP15 and VLX1570: A Paradigmatic Example of Unspecific Protein Crosslinking with Michael Acceptor Motif-Containing Drugs

31. Regulation of influenza A virus mRNA splicing by CLK1

32. The effect of house prices on household borrowing: a new approach

33. A Chemical Probe For Tudor Domain Protein Spindlin1 to Investigate Chromatin Functions

34. Rapid covalent-probe discovery by electrophile-fragment screening

35. Safety and efficacy of pharmacological cardioversion of recent-onset atrial fibrillation: a single-center experience

36. Reduced Ang2 expression in aging endothelial cells

37. Abstract 5808: Examination of clinically relevant inhibitor selectivity in live cells across the CDK family

38. Low-temperature plasma annealing of sputtered indium tin oxide for transparent and conductive thin-films on glass and polymer substrates

39. Rapid covalent-probe discovery by electrophile fragment screening

40. Discovery of an MLLT1/3 YEATS Domain Chemical Probe

41. Design, Synthesis and Characterization of Covalent KDM5 Inhibitors

42. Small molecule inhibitors reveal an indispensable scaffolding role of <scp>RIPK</scp> 2 in <scp>NOD</scp> 2 signaling

43. Statin treatment reduces matrix degradation capacity of proinflammatory polarized macrophages

44. Creation of a novel class of potent and selective MutT Homologue 1 (MTH1) inhibitors using fragment-based screening and structure-based drug design

45. A Chemical Biology Toolbox for the Study of Protein Methyltransferases and Epigenetic Signaling

46. Pharmacological targeting of the Wdr5-MLL interaction in C/EBPα N-terminal leukemia

47. SLC38A9 is a component of the lysosomal amino acid sensing machinery that controls mTORC1

48. Quantitative, wide-spectrum kinase profiling in live cells for assessing the effect of cellular ATP on target engagement

49. Isoform-selective ATAD2 chemical probe with novel chemical structure and unusual mode of action

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