93 results on '"Picaud, Sarah"'
Search Results
52. MOB1 Mediated Phospho-recognition in the Core Mammalian Hippo Pathway
53. Selective targeting of the BRG/PB1 bromodomains impairs embryonic and trophoblast stem cell maintenance
54. Discovery and Optimization of Small-Molecule Ligands for the CBP/p300 Bromodomains
55. Multivalent Histone and DNA Engagement by a PHD/BRD/PWWP Triple Reader Cassette Recruits ZMYND8 to K14ac-Rich Chromatin
56. Promiscuous targeting of bromodomains by bromosporine identifies BET proteins as master regulators of primary transcription response in leukemia
57. Discovery of New Bromodomain Scaffolds by Biosensor Fragment Screening
58. Identification of a Chemical Probe for Family VIII Bromodomains through Optimization of a Fragment Hit
59. Discovery of novel small-molecule inhibitors of BRD4 using structure-based virtual screening
60. BRAF/MAPK and GSK3 signaling converges to control MITF nuclear export.
61. A TFEB nuclear export signal integrates amino acid supply and glucose availability.
62. Synthesis and Biological Investigation of (+)-JD1, an Organometallic BET Bromodomain Inhibitor
63. Generation of a Selective Small Molecule Inhibitor of the CBP/p300 Bromodomain for Leukemia Therapy
64. Abstract IA19: Regulation of signaling interactomes in cancer
65. SPOTing Acetyl-Lysine Dependent Interactions
66. 9H-Purine Scaffold Reveals Induced-Fit Pocket Plasticity of the BRD9 Bromodomain
67. Targeting Aberrant Self-Renewal of Leukemic Cells with a Novel CBP/p300 Bromodomain Inhibitor
68. Abstract 5387: Dual kinase/bromodomain inhibitors for rationally designed polypharmacology
69. Erratum: Corrigendum: Dual kinase-bromodomain inhibitors for rationally designed polypharmacology
70. A Series of Potent CREBBP Bromodomain Ligands Reveals an Induced-Fit Pocket Stabilized by a Cation-π Interaction
71. Dual kinase-bromodomain inhibitors for rationally designed polypharmacology
72. Cloning and expression of a hexose transporter gene expressed during the ripening og grape berry
73. [1,2,4]Triazolo[4,3-a]phthalazines: Inhibitors of Diverse Bromodomains
74. PFI-1, a Highly Selective Protein Interaction Inhibitor, Targeting BET Bromodomains
75. Optimization of 3,5-Dimethylisoxazole Derivatives as Potent Bromodomain Ligands
76. Stimulation of Hepatic Apolipoprotein A-I Production by Novel Thieno-Triazolodiazepines: Roles of the Classical Benzodiazepine Receptor, PAF Receptor, and Bromodomain Binding
77. The design and synthesis of 5- and 6-isoxazolylbenzimidazoles as selective inhibitors of the BET bromodomains
78. Identification of a Chemical Probe for Bromo and Extra C-Terminal Bromodomain Inhibition through Optimization of a Fragment-Derived Hit
79. 3,5-Dimethylisoxazoles Act As Acetyl-lysine-mimetic Bromodomain Ligands
80. Bromodomain-peptide displacement assays for interactome mapping and inhibitor discovery
81. Crystal structure of human carbonic anhydrase-related protein VIII reveals the basis for catalytic silencing
82. Improved conditions for production of recombinant plant sesquiterpene synthases in Escherichia coli
83. 9H-PurineScaffold RevealsInduced-Fit Pocket Plasticity of the BRD9 Bromodomain.
84. Immunolocalization of the saposin‐like insert of plant aspartic proteinases exhibiting saposin C activity. Expression in young flower tissues and in barley seeds
85. Cloning and expression of two plasma membrane aquaporins expressed during the ripening of grape berry
86. [1,2,4]Triazolo[4,3-a]phthalazines:Inhibitors of Diverse Bromodomains.
87. Discovery of Novel Small-MoleculeInhibitors of BRD4Using Structure-Based Virtual Screening.
88. Optimizationof 3,5-Dimethylisoxazole Derivativesas Potent Bromodomain Ligands.
89. Identification of a ChemicalProbe for Bromo and ExtraC-Terminal Bromodomain Inhibition through Optimization of aFragment-Derived Hit.
90. Multivalent Histone and DNA Engagement by a PHD/BRD/PWWP Triple Reader Cassette Recruits ZMYND8 to K14ac-Rich Chromatin
91. Corrigendum: Dual kinase-bromodomain inhibitors for rationally designed polypharmacology.
92. Supertertiary structure analysis and comparison of BET proteins upon bivalent binding
93. 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.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.