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THPP target assignment reveals EchA6 as an essential fatty acid shuttle in mycobacteriaImproving Mycobacterium bovis bacillus Calmette-Guèrin as a vaccine delivery vector for viral antigens by incorporation of glycolipid activators of NKT cellsNovel inhibitors of Mycobacterium tuberculosis GuaB2 identified by a target based high-throughput phenotypic screenThe bovine CD1D gene has an unusual gene structure and is expressed but cannot present α-galactosylceramide with a C26 fatty acidA single subset of dendritic cells controls the cytokine bias of natural killer T cell responses to diverse glycolipid antigensCD1d-mediated activation of group 3 innate lymphoid cells drives IL-22 production.New CD1d agonists: synthesis and biological activity of 6″-triazole-substituted α-galactosyl ceramides.Design, synthesis, and functional activity of labeled CD1d glycolipid agonists.In contrast to other species, α-Galactosylceramide (α-GalCer) is not an immunostimulatory NKT cell agonist in horses.Towards multivalent CD1d ligands: synthesis and biological activity of homodimeric α-galactosyl ceramide analogues.Tether-directed synthesis of highly substituted oxasilacycles via an intramolecular allylation employing allylsilanes.Synthesis of a versatile building block for the preparation of 6-N-derivatized α-galactosyl ceramides: rapid access to biologically active glycolipids.Synthesis and biological activity of alpha-glucosyl C24:0 and C20:2 ceramides.Total synthesis and proof of relative stereochemistry of (-)-aureonitol.An appraisal of oxoketene cycloaddition methodology for the synthesis of 2,6-dideoxysugars and fluorinated 2,6-dideoxysugars.Temporary silicon connection strategies in intramolecular allylation of aldehydes with allylsilanes.A Brønsted acid mediated cascade enone synthesis from aldehydes containing a tethered propargylsilane.Photoactivable Glycolipid Antigens Generate Stable Conjugates with CD1d for Invariant Natural Killer T Cell ActivationStereoselective synthesis of 3,4-disubstituted tetrahydrofurans and 2,3,4-trisubstituted tetrahydrofurans using an intramolecular allylation strategy employing allylsilanesStereoselective Synthesis of 2,4,5-Trisubstituted Tetrahydropyrans Using an Intramolecular Allylation StrategyBiological Evaluation of Naproxen-Dehydrodipeptide Conjugates with Self-Hydrogelation Capacity as Dual LOX/COX InhibitorsDehydropeptide-based plasmonic magnetogels: a supramolecular composite nanosystem for multimodal cancer therapy
P50
Q27727961-AFA9BB48-9477-4AC4-85E8-C9A5396DEC13Q28543248-D7FD2748-51B2-44AA-80CB-7B1F67E16C8FQ28817264-2B826416-0F2F-4887-ABC9-176B40B5EAFBQ36749511-80997651-92C9-4C32-A882-12A2130E8567Q37491277-B8308E57-A134-4A73-9ECF-CA9F7645AAEEQ39230029-8179FD69-A410-4FC8-A8E7-91D41F93618AQ39339162-855F8371-4429-409B-9E3E-9F65DF8DB967Q39955940-AFC22CEC-5006-4915-9055-570FC64C8857Q41636681-9998ED3D-C403-4F76-8517-BD482D0E6074Q41841063-66F2AF5D-DBFC-42EF-92C8-2DC52A3162CBQ42081360-8B3EFA31-85ED-4F04-A1D3-3EE367BCD3F0Q42160618-0222A481-6C6D-49DD-B9C3-5ED6FA92FCAFQ42172806-9536ADDF-94A7-4D75-98E5-B26EA8AEAAB3Q44846634-929C80DD-8639-42CC-A4C6-067F4C7D5B58Q46063172-144731E1-C212-4DC1-8631-3D3DB9A2D68EQ46537282-111250A6-D2D3-4D44-B4D6-03F288CF3C00Q46806519-C47BC6F2-251F-4C8B-9754-2238E4B650E7Q63361216-2E25BCC2-8B4C-4DB7-B2A6-93EA4401D337Q63361236-3FA3F2E4-1247-4DEF-AE19-F61E732BAC48Q63361251-C3C54259-325D-4325-AD26-9D48A8EEE8D6Q89578237-37C4C5F8-10B1-4BCD-84EC-538096EFE5B3Q91437428-FEFAA7F8-CFF7-484E-BD23-332B2B1E2613
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Peter J Jervis
@ast
Peter J Jervis
@en
Peter J Jervis
@es
Peter J Jervis
@nl
type
label
Peter J Jervis
@ast
Peter J Jervis
@en
Peter J Jervis
@es
Peter J Jervis
@nl
prefLabel
Peter J Jervis
@ast
Peter J Jervis
@en
Peter J Jervis
@es
Peter J Jervis
@nl
P106
P21
P31
P496
0000-0002-5550-4535