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1. Acetylation reprograms MITF target selectivity and residence time

3. DNA damage remodels the MITF interactome to increase melanoma genomic instability

4. BRAF/MAPK and GSK3 signaling converges to control MITF nuclear export

6. BET bromodomain ligands: Probing the WPF shelf to improve BRD4 bromodomain affinity and metabolic stability

9. DNA damage-induced interaction between a lineage addiction oncogenic transcription factor and the MRN complex shapes a tissue-specific DNA Damage Response and cancer predisposition

10. Supplemental Methods and References from Generation of a Selective Small Molecule Inhibitor of the CBP/p300 Bromodomain for Leukemia Therapy

11. Supplementary Tables S1-S8 from Generation of a Selective Small Molecule Inhibitor of the CBP/p300 Bromodomain for Leukemia Therapy

12. Data from Generation of a Selective Small Molecule Inhibitor of the CBP/p300 Bromodomain for Leukemia Therapy

13. Supplemental Figures S1-S6 from Generation of a Selective Small Molecule Inhibitor of the CBP/p300 Bromodomain for Leukemia Therapy

14. Front Cover: Discovery of Benzo[d]imidazole‐6‐sulfonamides as Bromodomain and Extra‐Terminal Domain (BET) Inhibitors with Selectivity for the First Bromodomain (ChemMedChem 20/2022)

15. Discovery of Benzo[ d ]imidazole‐6‐sulfonamides as Bromodomain and Extra‐Terminal Domain (BET) Inhibitors with Selectivity for the First Bromodomain

19. Acetylation reprograms MITF target selectivity

20. Discovery of Novel BRD4 Ligand Scaffolds by Automated Navigation of the Fragment Chemical Space

21. The structure of nontypeable Haemophilus influenzae SapA in a closed conformation reveals a constricted ligand-binding cavity and a novel RNA binding motif

23. Controlling Intramolecular Interactions in the Design of Selective, High-Affinity Ligands for the CREBBP Bromodomain

24. Probing BRD Inhibition Substituent Effects in Bulky Analogues of (+)‐JQ1

26. BRD4 methylation by the methyltransferase SETD6 regulates selective transcription to control mRNA translation

28. Probing BRD Inhibition Substituent Effects in Bulky Analogues of (+)‐JQ1

30. Controlling Intramolecular Interactions in the Design of Selective, High-Affinity, Ligands for the CREBBP Bromodomain

31. Selective inhibition of BET bromodomains

32. Synthesis and Biological Investigation of (+)-JD1, an Organometallic BET Bromodomain Inhibitor

34. Interactome Rewiring Following Pharmacological Targeting of BET Bromodomains

36. A Tail-Based Mechanism Drives Nucleosome Demethylation by the LSD2/NPAC Multimeric Complex

37. Interactome Rewiring Following Pharmacological Targeting of BET Bromodomains

38. Evaluation of linker length effects on a BET bromodomain probe

40. Nut Directs p300-Dependent, Genome-Wide H4 Hyperacetylation in Male Germ Cells

41. Small molecule inhibitors reveal an indispensable scaffolding role of RIPK 2 in NOD 2 signaling

43. Promiscuous targeting of bromodomains by bromosporine identifies BET proteins as master regulators of primary transcription response in leukemia

44. Citrullination-acetylation interplay guides E2F-1 activity during the inflammatory response

45. The C-terminal extension landscape of naturally presented HLA-I ligands

48. Selective targeting of the BRG/PB1 bromodomains impairs embryonic and trophoblast stem cell maintenance

49. Multivalent Histone and DNA Engagement by a PHD/BRD/PWWP Triple Reader Cassette Recruits ZMYND8 to K14ac-Rich Chromatin

50. Synthesis and Biological Investigation of (+)-JD1, an Organometallic BET Bromodomain Inhibitor

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