Fedorov, Oleg.
Oleg Fedorov
Фёдоров, Олег
Фёдоров, О. иллюстратор Олег
Fiodorow, Oleg
Fedorov, Oleg P.
VIAF ID: 311284230 (Personal)
Permalink: http://viaf.org/viaf/311284230
Preferred Forms
- 100 1 _ ‡a Fedorov, Oleg
- 100 1 _ ‡a Fedorov, Oleg
- 100 1 _ ‡a Fedorov, Oleg
- 100 1 _ ‡a Fedorov, Oleg P.
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- 100 0 _ ‡a Oleg Fedorov
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4xx's: Alternate Name Forms (9)
Works
Title | Sources |
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7,8-Dichloro-1-oxo-β-carbolines as a Versatile Scaffold for the Development of Potent and Selective Kinase Inhibitors with Unusual Binding Modes | |
9 kompania [Dokument elektroniczny] / [kier. proj. Siergiej "Ulixes" Titarenko]. - Ostrów Wielkopolski, cop. 2008. | |
Arginine methylation-dependent reader-writer interplay governs growth control by E2F-1. | |
Bromo-deaza-SAH: a potent and selective DOT1L inhibitor | |
Bromodomain-peptide displacement assays for interactome mapping and inhibitor discovery | |
Chemical screening methods to identify ligands that promote protein stability, protein crystallization, and structure determination | |
The Cryptosporidium parvum Kinome | |
Crystal Structures of the p21-Activated Kinases PAK4, PAK5, and PAK6 Reveal Catalytic Domain Plasticity of Active Group II PAKs | |
The design and synthesis of 5- and 6-isoxazolylbenzimidazoles as selective inhibitors of the BET bromodomains | |
Discovery of Novel Small-Molecule Inhibitors of BRD4 Using Structure-Based Virtual Screening | |
Dziewiąta Kompania | |
Fragment Binding to the Nsp3 Macrodomain of SARS-CoV-2 Identified Through Crystallographic Screening and Computational Docking | |
Insights for the development of specific kinase inhibitors by targeted structural genomics | |
Kinase Domain Insertions Define Distinct Roles of CLK Kinases in SR Protein Phosphorylation | |
Kinase inhibitor selectivity profiling using differential scanning fluorimetry | |
Optimization of 3,5-Dimethylisoxazole Derivatives as Potent Bromodomain Ligands | |
PFI-1, a highly selective protein interaction inhibitor, targeting BET Bromodomains | |
Promiscuous targeting of bromodomains by bromosporine identifies BET proteins as master regulators of primary transcription response in leukemia. | |
Propionate analogues of zearalenone bind to Hsp90. | |
Resonance assignment of the RGS domain of human RGS10 | |
RhoB can adopt a Mg2+free conformation prior to GEF binding | |
RVX-208, an inhibitor of BET transcriptional regulators with selectivity for the second bromodomain | |
Samara : 81 arhitekturnyj šedevr : putevoditelʹ po sovremennoj arhitekture : 1917-2006= Samara : guide to modern architecture : 1917-2006, 2006 / Vitalij Stadnikov, Oleg Fedorov | |
Selective targeting of the BRG/PB1 bromodomains impairs embryonic and trophoblast stem cell maintenance. | |
Specific CLK Inhibitors from a Novel Chemotype for Regulation of Alternative Splicing | |
Structural analysis identifies imidazo[1,2-b]pyridazines as PIM kinase inhibitors with in vitro antileukemic activity | |
Structural basis of inhibitor specificity of the human protooncogene proviral insertion site in moloney murine leukemia virus (PIM-1) kinase | |
Structural Comparison of Human Mammalian Ste20-Like Kinases | |
Structural diversity in the RGS domain and its interaction with heterotrimeric G protein -subunits | |
Structural plasticity of histones H3-H4 facilitates their allosteric exchange between RbAp48 and ASF1 | |
Structure and regulation of the human Nek2 centrosomal kinase | |
Structure of dystrophia myotonica protein kinase | |
A systematic interaction map of validated kinase inhibitors with Ser/Thr kinases | |
Targeting Low-Druggability Bromodomains: Fragment Based Screening and Inhibitor Design against the BAZ2B Bromodomain | |
Topical antiangiogenic SRPK1 inhibitors reduce choroidal neovascularization in rodent models of exudative AMD | |
The (un)targeted cancer kinome | |
Use of Satellite and In-Situ Data to Improve Sustainability | |
Самара : 81 архитектурный шедевр : путеводитель по современной архитектуре : 1917-2006 = Samara :guide to modern architecture : 1917-2006 | |
Словод стихотворения | |
Янтарный ковчег |