about
Molecular Interactions of β-(1→3)-Glucans with Their ReceptorsBiological properties of (1 → 3)-β-D-glucan-based synthetic oligosaccharides.Identification of three elicitins and a galactan-based complex polysaccharide from a concentrated culture filtrate of Phytophthora infestans efficient against Pectobacterium atrosepticum.An ethoxylated surfactant enhances the penetration of the sulfated laminarin through leaf cuticle and stomata, leading to increased induced resistance against grapevine downy mildew.Recent progress in the field of beta-(1,3)-glucans and new applications.Recent knowledge and innovations related to hexofuranosides: structure, synthesis and applications.Specific and non-specific enzymes for furanosyl-containing conjugates: biosynthesis, metabolism, and chemo-enzymatic synthesis.The versatile enzyme Araf51 allowed efficient synthesis of rare pathogen-related β-D-galactofuranosyl-pyranoside disaccharides.Efficient gene transfer into human epithelial cell lines using glycosylated cationic carriers and neutral glycosylated co-lipids.Leishmania cell wall as a potent target for antiparasitic drugs. A focus on the glycoconjugates.Biocatalyzed synthesis of difuranosides and their ability to trigger production of TNF-α.Oligo-β-(1 → 3)-glucans: impact of thio-bridges on immunostimulating activities and the development of cancer stem cells.New 4-deoxy-(1→3)-β-D-glucan-based oligosaccharides and their immunostimulating potential.New oligo-beta-(1,3)-glucan derivatives as immunostimulating agents.Synthetic UDP-furanoses as potent inhibitors of mycobacterial galactan biogenesis.Synthesis and biological properties of galactofuranosyl-containing fluorescent dyes.Glucan-like synthetic oligosaccharides: iterative synthesis of linear oligo-beta-(1,3)-glucans and immunostimulatory effects.A single UDP-galactofuranose transporter is required for galactofuranosylation in Aspergillus fumigatus.4-Nitro-phenyl α-l-rhamnopyran-oside hemihydrateDouble diastereoselection explains limitations in synthesizing mannose-containing beta-(1,3)-glucans.Enzymatic synthesis of oligo-D-galactofuranosides and l-arabinofuranosides: from molecular dynamics to immunological assays.Synthetic UDP-furanoses inhibit the growth of the parasite Leishmania.Studies of a furanoside as antimycobacterial agent loaded into a biodegradable PBAT/sodium caseinate support.Cationic lipids derived from glycine betaine promote efficient and non-toxic gene transfection in cultured hepatocytes.Epoxidation of allylic alcohols in aqueous solutions of non surfactant amphiphilic sugars.A novel synthesis of D-galactofuranosyl, D-glucofuranosyl and D-mannofuranosyl 1-phosphates based on remote activation of new and free hexofuranosyl donors.A new synthesis of the oligosaccharide domain of acarbose.General one-step synthesis of free hexofuranosyl 1-phosphates using unprotected 1-thioimidoyl hexofuranosides.Probing UDP-galactopyranose mutase binding pocket: a dramatic effect on substitution of the 6-position of UDP-galactofuranose.Engineering ribonucleoside triphosphate specificity in a thymidylyltransferase.Synthesis of galactofuranose-containing disaccharides using thioimidoyl-type donorsThioimidoyl furanosides as first inhibitors of the alpha-L-arabinofuranosidase AbfD3Enzyme-catalyzed synthesis of furanosyl nucleotidesFirst o-glycosylation from unprotected 1-thioimidoyl hexofuranosides assisted by divalent cationsVersatile synthesis of rare nucleotide furanosesExploring the synthetic potency of the first furanothioglycoligase through original remote activationTwo-step synthesis of per-O-acetylfuranoses: optimization and rationalizationSynthesis and evaluation of 1,2-trans alkyl galactofuranoside mimetics as mycobacteriostatic agentsEfficient isomerization of methyl arabinofuranosides into corresponding arabinopyranosides in presence of pyridine6-Deoxy-6-fluoro galactofuranosides: regioselective glycosylation, unexpected reactivity, and anti-leishmanial activity
P50
Q26859196-DE460B89-36C8-4B8D-81A7-CE1F2AE82DCEQ33780741-79FC710E-A524-451E-9B38-224FDC6EAB2FQ35283939-C4E1ECF4-CFCE-4BF1-BD3F-B085B523CA2BQ35802920-64EDD000-C2D7-4FA5-B90C-97CFC273A3CEQ36683820-13806834-2772-42F9-A056-F29EE4C2C114Q37148970-E2C3B53F-15C6-4085-9214-598145B2A795Q38007228-57C6285E-AEC8-4904-A4AC-97CAC2970F98Q38307981-79366525-E439-4176-A205-6C30A4EE5342Q38344007-A15089D3-A301-4324-8441-10E4315B4C0FQ38541158-A0A3A859-E114-4F55-A468-7D022CA5A0EAQ38794130-22C3F442-E548-414B-9011-D0B40D618574Q38951971-6FB4B1FA-7D10-46D4-A24D-DF6017324F58Q39498313-F450D56D-DE29-4EA6-B968-4026F4B40AE3Q39774361-8DF54789-0A88-4015-9E90-BE06C76ADC07Q39804087-D49C247A-35CA-4F68-9084-C909833A9175Q40412771-70EBCB30-0A80-4605-B6BD-502EA30F4330Q40482148-F75DE210-B9CD-4ABF-A8B0-B600A421A64BQ41945725-7796DBF8-F2C7-4D0C-9021-9A26AB53FACDQ42766508-E527D85C-99DB-45E0-9FAD-DFFC40CCDA1EQ43062643-0309AF97-F690-4D25-B25F-2D6C0C7107DBQ43094628-060C2301-7B3B-4FC3-8C24-4E4C8365B1E5Q43123502-82824727-E1B3-4F59-A083-DAD931BEEBE1Q43709465-7A7F09AC-C61A-4B2F-BB59-DF12C24D7D3BQ44068998-936D0F9E-B6B6-4F65-A52E-5C2CE423063FQ44143428-A6F9CC59-565E-4013-89E7-2EF5BF4A50CAQ44223553-5B410F19-95B3-4ABD-81B2-15F2B7E03F96Q44687826-DFC31774-AD31-4F1C-A8D7-951FB1207C92Q45241458-5F83BBDC-5EF2-45FD-B435-EB5A9E1C03E5Q46177538-2E300F4A-C379-45BC-9C36-60AFC00913AFQ46461437-EFEC3AB2-4566-4119-BE34-DFF0FB9E49DCQ79286063-9CB0FF4F-7900-4CA5-A731-D6F56C5480F6Q79312686-50AE7331-5C0F-4C64-A78B-7E4D7A50B470Q80231632-997C158F-9A72-4800-BC53-29E89F9C7372Q80549400-17AC8606-E26C-4A58-B7FB-180D10B5D00CQ81588308-DC7B036F-A0B1-4701-A9CB-07DBA5ACF1EFQ82430961-035D047C-DD00-44B5-A441-337525895AAFQ83340415-53C44A1B-34F0-416F-AC92-D63EAB902D59Q86998636-A0FA70E1-4039-46B0-986D-CBC53DA1BE89Q87976482-5BF91177-EBFC-41B9-8A99-3818E2F794ABQ89561394-0DD756EF-C2DB-4271-87A8-769EF0156E9F
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Vincent Ferrières
@ast
Vincent Ferrières
@en
Vincent Ferrières
@es
Vincent Ferrières
@nl
Vincent Ferrières
@sl
type
label
Vincent Ferrières
@ast
Vincent Ferrières
@en
Vincent Ferrières
@es
Vincent Ferrières
@nl
Vincent Ferrières
@sl
prefLabel
Vincent Ferrières
@ast
Vincent Ferrières
@en
Vincent Ferrières
@es
Vincent Ferrières
@nl
Vincent Ferrières
@sl
P1053
B-4452-2009
P106
P21
P31
P3829
P496
0000-0002-2780-7774