about
End-stapled homo and hetero collagen triple helices: a click chemistry approach5-Hydroxyethyl-3-tetradecanoyltetramic acid represents a novel treatment for intravascular catheter infections due to Staphylococcus aureusTargeting Staphylococcus aureus quorum sensing with nonpeptidic small molecule inhibitors.Methicillin resistance reduces the virulence of healthcare-associated methicillin-resistant Staphylococcus aureus by interfering with the agr quorum sensing system.Virulence regulation and quorum sensing in staphylococcal infections: competitive AgrC antagonists as quorum sensing inhibitors.Modulation of pRB/E2F functions in the regulation of cell cycle and in cancer.Attenuating Staphylococcus aureus virulence gene regulation: a medicinal chemistry perspective.Look who's talking: communication and quorum sensing in the bacterial world.Protease sensing with nanoparticle based platforms.Thermoresponsive polymer colloids for drug delivery and cancer therapy.Controlled intracellular generation of reactive oxygen species in human mesenchymal stem cells using porphyrin conjugated nanoparticles.New Found Hope for Antibiotic Discovery: Lipid II Inhibitors.5-Carboxyfluorescein tagged N-phenylanthranilamide as a tracer reagent for fluorescence polarization: a robust method to screen MAPK pathway allosteric inhibitors.Targeting of polyamidoamine-DNA nanoparticles using the Staudinger ligation: attachment of an RGD motif either before or after complexation.Molecular mechanism of target recognition by subtilin, a class I lanthionine antibiotic.Regulation of neurotoxin production and sporulation by a Putative agrBD signaling system in proteolytic Clostridium botulinum.Antigenicity of chimeric and cyclic synthetic peptides based on nonstructural proteins of GBV-C/HGV.A facile method to clickable sensing polymeric nanoparticles.Facile synthesis of responsive nanoparticles with reversible, tunable and rapid thermal transitions from biocompatible constituents.Structure, activity and evolution of the group I thiolactone peptide quorum-sensing system of Staphylococcus aureus.Homochiral 4-azalysine building blocks: syntheses and applications in solid-phase chemistry.Peptide inhibitors of CDK2-cyclin A that target the cyclin recruitment-site: structural variants of the C-terminal Phe.Side-chain-to-tail thiolactone peptide inhibitors of the staphylococcal quorum-sensing system.Differential recognition of Staphylococcus aureus quorum-sensing signals depends on both extracellular loops 1 and 2 of the transmembrane sensor AgrC.Protease responsive nanoprobes with tethered fluorogenic peptidyl 3-arylcoumarin substrates.A facile approach to tryptophan derivatives for the total synthesis of argyrin analogues.Internally quenched peptides for the study of lysostaphin: An antimicrobial protease that kills Staphylococcus aureus.Rational design and synthesis of modified teixobactin analogues: in vitro antibacterial activity against Staphylococcus aureus, Propionibacterium acnes and Pseudomonas aeruginosa.Interaction of the lantibiotic nisin with mixed lipid bilayers: a 31P and 2H NMR studyStructure-activity relationships in the peptide antibiotic nisin: antibacterial activity of fragments of nisinProbing protein–peptide–protein molecular architecture by atomic force microscopy and surface plasmon resonanceA versatile polymer-supported 4-(4-Methylphenyl(chloro)methyl)phenoxy linker for solid-phase synthesis of pseudopeptidesTiming Is Everything: Impact of Naturally Occurring Staphylococcus aureus AgrC Cytoplasmic Domain Adaptive Mutations on Autoinduction
P50
Q27666402-5DA2C8F4-F868-4608-A0BB-B408640F33A3Q33589815-4AE7F04E-24DA-47EA-9EF7-13F3E6B18F7FQ35110055-4B034BC3-6BC5-4A45-BF9A-1B5EBA3314A0Q35868125-4DB4655E-A4A1-4105-B6BE-04FA6E2449EBQ35876322-61674013-6AF4-48E3-B4BC-E9C43E260B4EQ36126555-62259952-3048-4081-8D2B-3EC68778DA22Q36648854-51470CE2-46A2-4AE5-BFBA-405C8039F032Q36759802-B270CB80-49BF-4E1C-97F2-E750BEE3F233Q37793922-5BB1B538-FABE-4EBF-BB95-88EE4AFA650DQ37947523-43F8D1F8-6A51-4EFC-9388-689D685BAAB2Q38844808-9E6C3141-19F4-47D6-B69A-1759A2F319C2Q38889355-F5D4D583-BF5D-4B88-BD3F-7125320919F5Q39729131-45B59D10-CD60-4076-B911-B0626FA0A444Q39978551-78913941-A6AF-4178-B1B6-EBFB2DEDA574Q41915246-AE3A6F3F-9F9B-410F-89F2-76D29B14E519Q42738151-D201325A-F58C-44B5-A5D5-D8F8A864EA7EQ42995394-D6EEC81C-8A70-4D66-94F5-9749207E53C3Q43253064-B448FC21-8087-4A7E-8A82-288B5C5DF1C2Q43265999-AA815785-4436-4304-AC68-4E38E34370CAQ43698197-02635AA3-6D31-4FBD-BBBB-9DCFEF6254EFQ44021190-C564FD7E-D8D5-4D46-9CE6-E9D0B5F903C1Q44105387-3E6E5439-87E7-451B-8D7A-1DA5A9FF9498Q44508018-2A171B9F-FBE3-4C17-8087-58FF75BA45FCQ46517211-400AF699-5ACF-41C2-9DDE-AF04353AF0C3Q50598728-6D2C1BE0-C423-443A-806C-2D62D0619C57Q51039111-20D83398-D030-460C-8ED5-BE42033F5727Q53588360-22A7EF6B-5496-4BF0-A256-D1969B947EECQ54217425-90A287E2-AC77-428C-850F-DC528BB80762Q57102002-6638739F-0AD1-4E5C-AF65-0DA83CC31FA2Q58573572-543C8F0A-E65A-4A94-B312-EC903F2F3D0DQ58622625-A906AB00-2223-49E9-A084-B845A1ACDDA4Q74218602-1E3F15FC-FB2B-4230-A9E0-DD54AF550B3EQ92264592-AF8BE0EE-3B67-473C-8A66-757B5508A149
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Weng C. Chan
@ast
Weng C. Chan
@en
Weng C. Chan
@es
Weng C. Chan
@nl
Weng C. Chan
@sl
type
label
Weng C. Chan
@ast
Weng C. Chan
@en
Weng C. Chan
@es
Weng C. Chan
@nl
Weng C. Chan
@sl
prefLabel
Weng C. Chan
@ast
Weng C. Chan
@en
Weng C. Chan
@es
Weng C. Chan
@nl
Weng C. Chan
@sl
P1053
O-2045-2015
P106
P1153
7403918709
P31
P3829
P496
0000-0002-0488-825X
P569
2000-01-01T00:00:00Z