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2. Bromodomain inhibitor i-BET858 triggers a unique transcriptional response coupled to enhanced DNA damage, cell cycle arrest and apoptosis in high-grade ovarian carcinoma cells

8. Modulation of macrophage inflammatory function through selective inhibition of the epigenetic reader protein SP140

10. Influenza virus infection causes global RNAPII termination defects

12. Discovery of a first-in-class reversible DNMT1-selective inhibitor with improved tolerability and efficacy in acute myeloid leukemia

16. Brd4 bridges the transcriptional regulators, Aire and P-TEFb, to promote elongation of peripheral-tissue antigen transcripts in thymic stromal cells

17. Epigenetic modulation of type-1 diabetes via a dual effect on pancreatic macrophages and β cells.

18. Structure-Guided Design of a Domain-Selective Bromodomain and Extra Terminal N-Terminal Bromodomain Chemical Probe

19. Combined noncanonical NF-[kappa]B agonism and targeted BET bromodomain inhibition reverse HIV latency ex vivo

20. Remodeling of the Enhancer Landscape during Macrophage Activation Is Coupled to Enhancer Transcription

21. Click chemistry enables preclinical evaluation of targeted epigenetic therapies

22. Design and Characterization of 1,3-Dihydro-2H-benzo[d]azepin-2-ones as Rule-of-5 Compliant Bivalent BET Inhibitors

26. Supplementary Methods; Supplementary Figures S1-S6; and Supplementary Tables S1-S4 from Antileukemic Efficacy of BET Inhibitor in a Preclinical Mouse Model of MLL-AF4+ Infant ALL

27. Data from Antileukemic Efficacy of BET Inhibitor in a Preclinical Mouse Model of MLL-AF4+ Infant ALL

28. List of Contributors

30. Targeting enhancer switching overcomes non-genetic drug resistance in acute myeloid leukaemia

31. IL-10 Drives Glycolysis and Hinders Mitochondrial Pathways in Human Macrophages: Implications for Inflammatory Bowel Disease and Anti-TNF Treatment

32. SRPK1 maintains acute myeloid leukemia through effects on isoform usage of epigenetic regulators including BRD4

33. Identification and Optimization of a Ligand-Efficient Benzoazepinone Bromodomain and Extra Terminal (BET) Family Acetyl-Lysine Mimetic into the Oral Candidate Quality Molecule I-BET432

35. Acute resistance to BET inhibitors remodels compensatory transcriptional programs via p300 co-activation

37. A BET Protein Inhibitor Targeting Mononuclear Myeloid Cells Affects Specific Inflammatory Mediators and Pathways in Crohn’s Disease

38. Potent antimyeloma activity of the novel bromodomain inhibitors I-BET151 and I-BET762

40. Phase 1 and preclinical profiling of ESM‐HDAC391, a myeloid‐targeted histone deacetylase inhibitor, shows enhanced pharmacology and monocytopaenia

43. Combined noncanonical NF-κB agonism and targeted BET bromodomain inhibition reverse HIV latency ex vivo

44. Selective inhibitors of bromodomain BD1 and BD2 of BET proteins modulate radiation‐induced profibrotic fibroblast responses

45. Additional file 16 of Modulation of macrophage inflammatory function through selective inhibition of the epigenetic reader protein SP140

46. Design, Synthesis, and Characterization of I-BET567, a Pan-Bromodomain and Extra Terminal (BET) Bromodomain Oral Candidate

48. Carboxylesterase-1 Assisted Targeting of HDAC Inhibitors to Mononuclear Myeloid Cells in Inflammatory Bowel Disease

49. BET inhibitor resistance emerges from leukaemia stem cells

50. Discovery of a Novel Bromodomain and Extra Terminal Domain (BET) Protein Inhibitor, I-BET282E, Suitable for Clinical Progression

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