308 results on '"Rotili, D"'
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2. Y3+ embedded in polymeric nanoparticles: Morphology, dimension and stability of composite colloidal system
3. Molecular insights into RmcA-mediated c-di-GMP consumption: Linking redox potential to biofilm morphogenesis in Pseudomonas aeruginosa
4. Molecular insights into RmcA-mediated c-di-GMP consumption: Linking redox potential to biofilm morphogenesis in Pseudomonas aeruginosa
5. Hydrophilic Gold Nanoparticles as Anti-PD-L1 Antibody Carriers: Synthesis and Interface Properties
6. JQ1, inibitore delle proteine BET, riduce i fattori di virulenza e la patogenicità di Aspergillus fumigatus
7. 6-(Arylmethyl)pyrimidin-4(3H)-ones: anthology and prospects of highly efficient anti-HIV agents
8. The specific character of the reaction of derivatives of 2-thioxo-2,3-dihydropyrimidin-4(1H)-one with iodomethane and alkyl chloromethyl sulfides
9. Stereoselective synthesis of 2-substituted 6-[1-(2,6-difluorophenyl)ethyl]-5-methylpyrimidin-4(3H)-ones
10. Reactions of 6-benzyl-5-methyl-2-(methylsulfanyl)pyrimidin-4(3H)-one with aliphatic and aliphatic-aromatic amines
11. Salermide, a Sirtuin inhibitor with a strong cancer-specific proapoptotic effect
12. Epigenetic modulators as a new strategies to reduce Aspergillus pathogenicity
13. Effect of alpha-Methoxy Substitution on the Anti-HIV Activity of Dihydropyrimidin-4(3H)-ones
14. Histone deacetylase inhibitors exert anti-tumor effects on human adherent and stem-like glioma cells 11 Medical and Health Sciences 1112 Oncology and Carcinogenesis
15. Inhibition of Histone Demethylases LSD1 and UTX Regulates ER alpha Signaling in Breast Cancer
16. H19-Dependent Transcriptional Regulation of beta 3 and beta 4 Integrins Upon Estrogen and Hypoxia Favors Metastatic Potential in Prostate Cancer
17. RIP1-HAT1-SIRT Complex Identification and Targeting in Treatment and Prevention of Cancer
18. Erratum: Salermide, a Sirtuin inhibitor with a strong cancer-specific proapoptotic effect
19. Vegetative and reproductive development of shoots of different order of three maize hybrids at two contrasting population densities
20. Crystal structure of the catalytic domain of human JARID1B in complex with MC3948
21. EZH2 methyltransferase and JMJD3/UTX demethylases are involved in hepatocytic differentiation and liver cancer cells plasticity
22. Nitrobenzoxadiazoles exert anti-melanoma activity modulating the MAPK/JNK signalling
23. A novel orally active water-soluble inhibitor of human glutathione transferase exerts a potent and selective antitumor activity against human melanoma xenografts
24. A novel water-soluble nitrobenzoxadiazole is highly effective against vemurafenib-resistant human melanoma cells
25. Evaluation of histone deacetylases as drug targets in Huntington's disease models. Study of HDACs in brain tissues from R6/2 and CAG140 knock-in HD mouse models and human patients and in a neuronal HD cell model
26. HDACs class II selective inhibition alters nuclear receptor dependent differentiation
27. Hydroxamic acid-containing histone deacetylase inhibitors potentiate the antiproliferative and apoptotic effects induced by the ribonucleotide reductase R1 inhibitor 3'-C-methyl-adenosine in promyelocytic leukemia cell lines
28. Histone deacetylase (HDAC) inhibitors potentiate the antiproliferative and apoptotic effects induced by the novel ribonucleotide reductase (RR) inhibitor 3'-metil-adenosine (3'-Me-Ado) in promyelocitic leukemia cell lines
29. Identification of two New Synthetic Histone Deacetylase Inhibitors that Modulate Globin Gene Expression in Erythroid Cells from Normal Donors and Thalassemic Patients
30. LSD1-CoREST1 in complex with polymyxin E (colistin)
31. LSD1-CoREST1 in complex with quinazoline-derivative reversible inhibitor
32. LSD1-CoREST1 in complex with polymyxin B
33. Selective inhibition of HDAC1 and HDAC2 counteracts medulloblastoma cell growth in mouse models through Gli acetylation
34. Class II (IIa)-Selective Histone Deacetylase Inhibitors: Synthesis and Biological Evaluation of Novel (Aryloxopropenyl)pyrrolyl Hydroxyamides
35. Context-selective death of acute myeloid leukemia cells triggered by the novel hybrid retinoid-hdac inhibitor mc2392
36. Chiral HPLC Separation and Absolute Configuration of Novel S-DABO Derivatives
37. Class II HDACs function is required during the nitric oxide-dependent early stage of embryonic stem cells cardiovascular differentiation
38. A novel Gcn5p inhibitor represses cell growth, gene transcription and histone acetylation in budding yeast
39. Epigenetic drugs targeting cccDNA-bound chromatin modifying enzymes silence HBV transcription and inhibit viral replication
40. 640 - Selective inhibition of HDAC1 and HDAC2 counteracts medulloblastoma cell growth in mouse models through Gli acetylation
41. Proteomic profile of differentially expressed plasma proteins from dystrophic mice and following suberoylanilide hydroxamic acid treatment
42. Nitric oxide determines mesodermic differentiation of mouse embryonic stem cells by activating class IIa histone deacetylases: potential therapeutic implications in a mouse model of hindlimb ischemia
43. ChemInform Abstract: 6‐(Arylmethyl)pyrimidin‐4(3H)‐ones: Anthology and Prospects of Highly Efficient anti‐HIV Agents
44. 56 SUPPRESSION OF HEPATITIS B VIRUS (HBV) TRANSCRIPTION AND REPLICATION BY SMALL MOLECULES THAT TARGET THE EPIGENETIC CONTROL OF NUCLEAR cccDNA MINICHROMOSOME
45. 1283 MC2791, A SPECIFIC Sirt1 AGONIST DRUG, DECREASES LIPIDS AND REACTIVE OXYGEN SPECIES ACCUMULATION IN AN IN VITRO MODEL OF STEATOSIS IN DIFFERENTIATED HepaRG CELLS
46. T-25 MC2791, a specific class III HDAC Sirt1 agonist drug, decreases lipids and reactive oxygen species accumulation in an in vitro model of steatosis in differentiated HepaRG cells
47. OC-22 Suppression of HBV transcription and replication by small molecules that target the epigenetic control of nuclear cccDNA minichromosome
48. PARP-1 inhibition decreases Beta-Amyloid-induced neurodegeneration: a cellular and animal model study
49. Targeting Histone Demethylases: A New Avenue for the Fight against Cancer
50. ChemInform Abstract: The Specific Character of the Reaction of Derivatives of 2-Thioxo-2,3-dihydropyrimidin-4(1H)-one with Iodomethane and Alkyl Chloromethyl Sulfides.
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