33 results on '"Chory, Emma"'
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2. RNA-responsive elements for eukaryotic translational control
3. Systematic molecular evolution enables robust biomolecule discovery
4. Random adversarial threshold search enables automated DNA screening
5. A Deep Learning Approach to Antibiotic Discovery
6. Nucleosome Turnover Regulates Histone Methylation Patterns over the Genome
7. Chemically induced proximity in biology and medicine
8. Enabling high‐throughput biology with flexible open‐source automation
9. Low-cost camera-based estrous tracking enables transgenesis inPeromyscus leucopus, the primary reservoir for Lyme disease
10. High-throughput Approaches to Uncover Synergistic Drug Combinations in Leukemia
11. High-throughput Approaches to Uncover Synergistic Drug Combinations in Leukemia
12. Dynamics of BAF–Polycomb complex opposition on heterochromatin in normal and oncogenic states
13. Dynamic Opposition of Histone Modifications
14. Dynamic Opposition of Histone Modifications.
15. Systematic molecular evolution enables robust biomolecule discovery
16. RNA-responsive elements for eukaryotic translational control
17. A high-throughput platform for feedback-controlled directed evolution
18. Enabling high‐throughput biology with flexible open‐source automation
19. Chemical Inhibitors of a Selective SWI/SNF Function Synergize with ATR Inhibition in Cancer Cell Killing
20. Flexible open-source automation for robotic bioengineering
21. A high-throughput platform for feedback-controlled directed evolution
22. A Deep Learning Approach to Antibiotic Discovery
23. Catalytic site remodelling of the DOT1L methyltransferase by selective inhibitors
24. Inhibition of a Selective SWI/SNF Function Synergizes with ATR Inhibitors in Cancer Cell Killing
25. Nucleosome turnover is sufficient to establish varied histone methylation states
26. Rapid and reversible epigenome editing by endogenous chromatin regulators
27. Dynamics of BAF–Polycomb complex opposition on heterochromatin in normal and oncogenic states
28. Structure-Guided DOT1L Probe Optimization by Label-Free Ligand Displacement
29. p38 Signaling and Receptor Recycling Events in a Microfluidic Endothelial Cell Adhesion Assay
30. Correction: Corrigendum: Catalytic site remodelling of the DOT1L methyltransferase by selective inhibitors
31. Separation of two phenotypically similar cell types via a single common marker in microfluidic channels
32. Structure-Guided DOT1L Probe Optimization by Label-Free Ligand Displacement
33. Corrigendum: Catalytic site remodelling of the DOT1L methyltransferase by selective inhibitors.
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