814 results on '"Kutateladze, Tatiana G."'
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2. Molecular insight into interactions between the Taf14, Yng1 and Sas3 subunits of the NuA3 complex
3. ASXLs binding to the PHD2/3 fingers of MLL4 provides a mechanism for the recruitment of BAP1 to active enhancers
4. Circadian rhythms are set by epigenetic marks in neurons
5. HBO1, a MYSTerious KAT and its links to cancer
6. Molecular basis for nuclear accumulation and targeting of the inhibitor of apoptosis BIRC2
7. MLL4 binds TET3
8. The winged helix domain of MORF binds CpG islands and the TAZ2 domain of p300
9. Histone H4K16ac Binding Function of the Triple PHD Finger Cassette of MLL4
10. MORF and MOZ acetyltransferases target unmethylated CpG islands through the winged helix domain
11. Enzymatic Reactions inside Biological Condensates
12. Principles of assembly and regulation of condensates of Polycomb repressive complex 1 through phase separation
13. Differences and similarities in recognition of co-factors by Taf14
14. Design of thienopyranone-based BET inhibitors that bind multiple synthetic lethality targets.
15. Non-histone binding functions of PHD fingers
16. Chemical tools targeting readers of lysine methylation
17. Atypical histone targets of PHD fingers
18. Engaging with benzoyllysine through a π-π-π mechanism
19. Catching BETs by viruses
20. Binding of the SARS-CoV-2 envelope E protein to human BRD4 is essential for infection
21. Dusquetide modulates innate immune response through binding to p62
22. The ZZ domain of HERC2 is a receptor of arginylated substrates
23. Taf2 mediates DNA binding of Taf14
24. Combinatorial inhibition of BTK, PI3K-AKT and BRD4-MYC as a strategy for treatment of mantle cell lymphoma
25. SRX3177, a CDK4/6-PI3K-BET inhibitor, in combination with an RdRp inhibitor, Molnupiravir, or an entry inhibitor MU-UNMC-2, has potent antiviral activity against the Omicron Variant of SARS-CoV-2
26. Mechanistic similarities in recognition of histone tails and DNA by epigenetic readers
27. The BTK/PI3K/BRD4 axis inhibitor SRX3262 overcomes Ibrutinib resistance in mantle cell lymphoma
28. Suppression of canonical TGF-β signaling enables GATA4 to interact with H3K27me3 demethylase JMJD3 to promote cardiomyogenesis
29. Characterization of functional disordered regions within chromatin-associated proteins
30. KAP1 Is a Chromatin Reader that Couples Steps of RNA Polymerase II Transcription to Sustain Oncogenic Programs
31. Guiding the HBO1 complex function through the JADE subunit
32. Principles of assembly and regulation of condensates of Polycomb repressive complex 1 through phase separation
33. Sparse CBX2 nucleates many Polycomb proteins to promote facultative heterochromatinization of Polycomb target genes
34. Mechanism for autoinhibition and activation of the MORC3 ATPase
35. Nuclear condensates of p300 formed though the structured catalytic core can act as a storage pool of p300 with reduced HAT activity
36. The role of the PZP domain of AF10 in acute leukemia driven by AF10 translocations
37. MORC3 Forms Nuclear Condensates through Phase Separation
38. A Chromatin-Dependent Role of the Fragile X Mental Retardation Protein FMRP in the DNA Damage Response
39. Exploring epigenetics with chemical tools
40. Architecture of PRC2 Holo Complexes
41. Targeting of the FYVE Domain to Endosomal Membranes Is Regulated by a Histidine Switch
42. Dual-activity PI3K–BRD4 inhibitor for the orthogonal inhibition of MYC to block tumor growth and metastasis
43. Preclinical activity of a novel multi-axis inhibitor in aggressive and indolent B-cell malignancies
44. Covalent Modifications of Histone H3K9 Promote Binding of CHD3
45. A Unique pH-Dependent Recognition of Methylated Histone H3K4 by PPS and DIDO
46. The SET1 Complex Selects Actively Transcribed Target Genes via Multivalent Interaction with CpG Island Chromatin
47. Structural Insight into Recognition of Methylated Histone H3K4 by Set3
48. Molecular mechanism of the MORC4 ATPase activation
49. Inhibition of translation and immune responses by the virulence factor Nsp1 of SARS-CoV-2
50. A triple action CDK4/6-PI3K-BET inhibitor with augmented cancer cell cytotoxicity
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