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1. Supplementary Table 3 from PARP1 Trapping by PARP Inhibitors Drives Cytotoxicity in Both Cancer Cells and Healthy Bone Marrow

2. Supplementary Table 4 from PARP1 Trapping by PARP Inhibitors Drives Cytotoxicity in Both Cancer Cells and Healthy Bone Marrow

3. Supplementary Figure 2 from PARP1 Trapping by PARP Inhibitors Drives Cytotoxicity in Both Cancer Cells and Healthy Bone Marrow

4. Supplementary Figure 1 from PARP1 Trapping by PARP Inhibitors Drives Cytotoxicity in Both Cancer Cells and Healthy Bone Marrow

5. Supplementary Table 2 from PARP1 Trapping by PARP Inhibitors Drives Cytotoxicity in Both Cancer Cells and Healthy Bone Marrow

6. Data from PARP1 Trapping by PARP Inhibitors Drives Cytotoxicity in Both Cancer Cells and Healthy Bone Marrow

7. Supplementary Table 1 from PARP1 Trapping by PARP Inhibitors Drives Cytotoxicity in Both Cancer Cells and Healthy Bone Marrow

8. Discovery of a Potent Chloroacetamide GPX4 Inhibitor with Bioavailability to Enable Target Engagement in Mice, a Potential Tool Compound for Inducing Ferroptosis In Vivo

9. Discovery of a selective catalytic p300/CBP inhibitor that targets lineage-specific tumours

10. Creation of a Bacterial Cell Controlled by a Chemically Synthesized Genome

16. Author Correction: Discovery of a selective catalytic p300/CBP inhibitor that targets lineage-specific tumours

19. Discovery of a Potent and Selective Covalent p300/CBP Inhibitor

23. Cloning whole bacterial genomes in yeast

25. PARP1 Trapping by PARP Inhibitors Drives Cytotoxicity in Both Cancer Cells and Healthy Bone Marrow

26. SAR and characterization of non-substrate isoindoline urea inhibitors of nicotinamide phosphoribosyltransferase (NAMPT)

27. SAR of amino pyrrolidines as potent and novel protein-protein interaction inhibitors of the PRC2 complex through EED binding

28. Dissociation of eIF1 from the 40S ribosomal subunit is a key step in start codon selection in vivo

29. Abstract LB-A23: Discovery of a potent catalytic p300/CBP inhibitor that targets lineage-specific tumors

30. Erratum: The EED protein–protein interaction inhibitor A-395 inactivates the PRC2 complex

31. Discovery of a selective catalytic p300/CBP inhibitor that targets lineage-specific tumours

32. The EED protein–protein interaction inhibitor A-395 inactivates the PRC2 complex

33. The SUV4-20 inhibitor A-196 verifies a role for epigenetics in genomic integrity

35. Discovery of A-893, A New Cell-Active Benzoxazinone Inhibitor of Lysine Methyltransferase SMYD2

36. Synthetic Generation of Influenza Vaccine Viruses for Rapid Response to Pandemics

44. A Type III restriction-modification system in Mycoplasma mycoides subsp. capri

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