about
Ppm1-encoded polyprenyl monophosphomannose synthase activity is essential for lipoglycan synthesis and survival in mycobacteriaImproving Mycobacterium bovis bacillus Calmette-Guèrin as a vaccine delivery vector for viral antigens by incorporation of glycolipid activators of NKT cellsActivation of iNKT cells by a distinct constituent of the endogenous glucosylceramide fraction.Recognition of microbial and mammalian phospholipid antigens by NKT cells with diverse TCRs.Role for lysosomal phospholipase A2 in iNKT cell-mediated CD1d recognition.The bovine CD1D gene has an unusual gene structure and is expressed but cannot present α-galactosylceramide with a C26 fatty acidEndoplasmic reticulum glycoprotein quality control regulates CD1d assembly and CD1d-mediated antigen presentationDisruption of the serine/threonine protein kinase H affects phthiocerol dimycocerosates synthesis in Mycobacterium tuberculosis.Synthesis of a novel alpha-galactosyl ceramide haptenated-lipid antigen, a useful tool in demonstrating the involvement of iNKT cells in the production of antilipid antibodies.Saposins modulate human invariant Natural Killer T cells self-reactivity and facilitate lipid exchange with CD1d molecules during antigen presentation.A 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.Synthesis and biological activity of alpha-galactosyl ceramide KRN7000 and galactosyl (alpha1-->2) galactosyl ceramide.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.Amide analogues of CD1d agonists modulate iNKT-cell-mediated cytokine productionNon-glycosidic compounds can stimulate both human and mouse iNKT cells.Preparation, characterisation and entrapment of a non-glycosidic threitol ceramide into liposomes for presentation to invariant natural killer T cells.Reaction of 1,1'-divinyl ferrocene with one-electron oxidants: entry into functionalised [4]ferrocenophanes and observation of an isotope-dependent chemoselectivity effect.Synthesis of hybrid masked triyne-phenylene axial rods containing (E)-beta-chlorovinylsilanes in the pi-conjugated framework.Total synthesis and proof of relative stereochemistry of (-)-aureonitol.Stereoselective synthesis of allyl-C-mannosyl compounds: use of a temporary silicon connection in intramolecular allylation strategies with allylsilanes.Temporary silicon connection strategies in intramolecular allylation of aldehydes with allylsilanes.A Brønsted acid mediated cascade enone synthesis from aldehydes containing a tethered propargylsilane.Beta-chlorovinylsilanes as masked alkynes in oligoyne assembly: synthesis of the first aryl-end-capped dodecayne.Stereoselective synthesis of 2-dienyl-substituted piperidines using an eta4-dienetricarbonyliron complex as the stereocontrolling element in a double reductive amination cascade.Ultrasound-induced emulsification of subcritical carbon dioxide/water with and without surfactant as a strategy for enhanced mass transport.Identification and characterization of aspartyl-tRNA synthetase inhibitors against Mycobacterium tuberculosis by an integrated whole-cell target-based approachPhotoactivable Glycolipid Antigens Generate Stable Conjugates with CD1d for Invariant Natural Killer T Cell ActivationStereoselective Synthesis of 2,4,5-Trisubstituted Tetrahydropyrans Using an Intramolecular Allylation StrategyStereoselective Synthesis of 2-Dienyl-Substituted Pyrrolidines Using an η4-Dienetricarbonyliron Complex as the Stereodirecting Element: Elaboration to the Pyrrolizidine SkeletonRegio- and stereoselective hydrosilylation of terminal alkynes using Grubbs' first-generation olefin-metathesis catalystα-Amino acid synthesis via a Cu(II) chiral Lewis acid mediated addition of soft carbon nucleophiles to glycine cation equivalentsCatalytic Asymmetric Synthesis of a 1-Deoxy-1,1-difluoro-d-xyluloseStereoselective Synthesis of β-(Chloro)vinylsilanes Using a Regio- and (E)-Stereoselective Bis-Stannylation of Unsymmetrically Substituted Butadiynes: Application to the Synthesis of a Masked Triyne
P50
Q28484652-C4C35660-292E-486C-A5E3-F351FEBFDD7CQ28543248-BACEECDE-A133-44D5-AED3-138CFB9F63AEQ34218428-780931CF-787F-4DF4-AA1A-B1A46B903856Q36583205-4730D59A-F746-4171-9EAD-5619113B3CB6Q36729593-A681B500-F7FA-4D89-AD2C-52B9E203AED3Q36749511-9D3CBD36-AE10-4E91-858F-3DF37D24B918Q36910045-B9173998-B4B3-4C79-8E69-979CAF9DA7F6Q37007462-2C48A0B6-3AEE-42F3-98BA-E44D93FB5C15Q37322551-9A2AA90D-4E68-49AF-9C81-B468F472612BQ37377504-A55D3CAF-8F74-4894-9B8C-2E264B24542BQ37491277-BB45A1DC-DC3E-46E2-B652-B24C4C1D257CQ39230029-F68EEB20-DC4C-44AA-818F-340810E395F5Q39339162-04FD8BC0-C8AD-444C-8430-B2A26BD12CECQ39841856-B59FF753-26F5-444E-9D35-FE9C2884514CQ39955940-C81F00E9-A038-4323-952D-9652F77C7ADFQ41636681-644DD774-53F5-4846-9911-49981D532805Q41841063-844F23A1-DC2A-4FEC-A774-3209311CA3E1Q42081360-D721921A-8CF6-4542-A3C6-D90B1FE0C80BQ42160618-0C36F45D-5136-4F7F-A2B2-AD08B08980D0Q42172806-E8C57F40-82EA-4D79-A215-FC772FB72557Q42257577-CBEEA54D-AA9B-4585-A3FA-40C410BF506BQ42608724-AC33A548-21D8-4AD5-865F-F3AFB367E3E0Q42920496-45F14409-ECF7-4E1A-8651-84028EAD3E81Q43099938-26F5450A-63FA-4C63-A5A9-B05EB84A44FDQ43265142-9C98F3F3-752B-43C6-811B-0FB8BA124AA4Q44846634-10E21568-BD4B-4490-8C7D-7B3F80E712B6Q45051693-A2D20730-4750-4EEA-B0E4-1DFE4CFFC6BEQ46537282-FDA27C61-EE1C-4D62-9EFD-9E1B489C6E5BQ46806519-6C8FCEBA-E52B-4A0A-847F-48F857D6C740Q46969886-F6D420EE-D630-4DD7-80A3-41D84FDA49EEQ46969918-741A7689-6E54-4F9C-B10A-469975A5146DQ51802867-3661BDB2-0A5F-415E-86C1-8EA1D3AB06A9Q57093867-4E085195-A0CE-4C9C-8250-D36A679A4E08Q63361216-D0D71494-7C16-4A29-81E8-E71A02401771Q63361251-0381CC49-2E0C-4BE2-8937-43EBB05C8DE3Q63361257-78D33DB8-C373-4644-9BD4-72286E77F2E5Q63361269-65CD66DF-5CA6-43AA-8950-2EA3E32CB471Q63361271-00A7065E-6222-4C4F-9BC7-D5C288A9236BQ63361279-BCB0993D-456D-4EA0-9F71-F828074367DAQ63361283-E1D3E475-F004-4B8B-B650-DE7F8D04D880
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Liam R. Cox
@ast
Liam R. Cox
@en
Liam R. Cox
@es
Liam R. Cox
@nl
Liam R. Cox
@sl
ليام آر. كوكس
@ar
type
label
Liam R. Cox
@ast
Liam R. Cox
@en
Liam R. Cox
@es
Liam R. Cox
@nl
Liam R. Cox
@sl
ليام آر. كوكس
@ar
prefLabel
Liam R. Cox
@ast
Liam R. Cox
@en
Liam R. Cox
@es
Liam R. Cox
@nl
Liam R. Cox
@sl
ليام آر. كوكس
@ar
P108
P106
P1153
7202677662
P21
P31
P496
0000-0001-7018-3904