44 results on '"Kireev, Dmitri B."'
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2. The entropic lock and key of the histone code
3. Efforts toward discovering inhibitors of the SYK SH2–FCER1γ interaction as potential Alzheimer’s disease chemical probes and therapeutics
4. Discovery of selective activators of PRC2 mutant EED-I363M
5. Screening for Inhibitors of Low-Affinity Epigenetic Peptide-Protein Interactions: An AlphaScreen™-Based Assay for Antagonists of Methyl-Lysine Binding Proteins
6. Use of AD Informer Set compounds to explore validity of novel targets in Alzheimer's disease pathology
7. AD Informer Set: Chemical tools to facilitate Alzheimer's disease drug discovery
8. Generation of the AD Informer Set: Chemical tools to facilitate Alzheimer’s disease drug discovery
9. AD Informer Set: Chemical tools to facilitate Alzheimer’s disease drug discovery
10. REPROGRAMMING CBX8-PRC1 FUNCTION WITH A POSITIVE ALLOSTERIC MODULATOR
11. A CoMFA Study of Enantiomeric Organophoshorus Inhibitors of Acetylcholinesterase
12. Automated docking of 82 N-benzylpiperidine derivatives to mouse acetylcholinesterase and comparative molecular field analysis with 'natural' alignment
13. Design and Construction of a Focused DNA-Encoded Library for Multivalent Chromatin Reader Proteins
14. 3D Model of the Acetylcholinesterase Catalytic Cavity Probed by Stereospecific Organophosphorous Inhibitors
15. Discovery and Characterization of a Cellular Potent Positive Allosteric Modulator of the Polycomb Repressive Complex 1 Chromodomain, CBX7
16. Synthesis and Antibacterial Evaluation of Cephalosporin Isosteres
17. Correction to “Quantitative Characterization of Bivalent Probes for a Dual Bromodomain Protein, Transcription Initiation Factor TFIID subunit 1”
18. Quantitative Characterization of Bivalent Probes for a Dual Bromodomain Protein, Transcription Initiation Factor TFIID Subunit 1
19. Towards the development of a chemical probe targeting the disruption of SYK tandem SH2 domain and FCεR1γ interactions for Alzheimer's disease.
20. Chromodomain Ligand Optimization via Target-Class Directed Combinatorial Repurposing
21. Small-Molecule Ligands of Methyl-Lysine Binding Proteins: Optimization of Selectivity for L3MBTL3
22. Protein Lysine Methyltransferase G9a Inhibitors: Design, Synthesis, and Structure Activity Relationships of 2,4-Diamino-7-aminoalkoxy-quinazolines.
23. Small-molecule ligands of methyl-lysine binding proteins: Optimization of selectivity for L3MBTL3
24. Abstract SY08-03: Targeting chromatin regulation for cancer therapy: progress towards chemical probes for methyl-lysine readers
25. Potent, Selective, and Cell-active Chemical Probe of Protein Lysine Methyltransferases G9a and GLP: Cell-Based Assays
26. Non-supervised Neural Networks: A New Classification Tool to Process Large Databases
27. Small-Molecule Ligands of Methyl-Lysine Binding Proteins: Optimization of Selectivity for L3MBTL3
28. Abstract PR03: Multivalent histone engagement by the linked tandem Tudor and PHD domains of UHRF1 is required for DNA methylation maintenance
29. Multivalent histone engagement by the linked tandem Tudor and PHD domains of UHRF1 is required for the epigenetic inheritance of DNA methylation
30. Discovery of a chemical probe for the L3MBTL3 methyllysine reader domain
31. The structure–activity relationships of L3MBTL3 inhibitors: flexibility of the dimer interface
32. Structure–activity relationships of methyl-lysine reader antagonists
33. Erratum: A chemical probe selectively inhibits G9a and GLP methyltransferase activity in cells
34. A chemical probe selectively inhibits G9a and GLP methyltransferase activity in cells
35. Small-Molecule Ligands of Methyl-Lysine Binding Proteins
36. Protein Lysine Methyltransferase G9a Inhibitors: Design, Synthesis, and Structure Activity Relationships of 2,4-Diamino-7-aminoalkoxy-quinazolines.
37. Discovery of a 2,4-Diamino-7-aminoalkoxyquinazoline as a Potent and Selective Inhibitor of Histone Lysine Methyltransferase G9a
38. A 3D QSAR Study of a Series of HEPT Analogues: The Influence of Conformational Mobility on HIV-1 Reverse Transcriptase Inhibition
39. The molecular modeling and QSAR study of anti-HIV-1 2-heteroaryl-quinoline-4-amines
40. Small-MoleculeLigands of Methyl-Lysine Binding Proteins:Optimization of Selectivity for L3MBTL3.
41. Complete Thermodynamic Description of H‐Bonding in the Framework of Multiplicative Approach
42. Effects of Aloe vera Flower Extract and Its Active Constituent Isoorientin on Skin Moisturization via Regulating Involucrin Expression: In Vitro and Molecular Docking Studies.
43. AD Informer Set: Chemical tools to facilitate Alzheimer's disease drug discovery.
44. Use of AD Informer Set compounds to explore validity of novel targets in Alzheimer's disease pathology.
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