about
The Cyclic Cystine Ladder in -Defensins Is Important for Structure and Stability, but Not Antibacterial ActivityThe cyclic cystine ladder of theta-defensins as a stable, bifunctional scaffold: A proof-of-concept study using the integrin-binding RGD motifTransforming conotoxins into cyclotides: Backbone cyclization of P-superfamily conotoxinsMirror Images of Antimicrobial Peptides Provide Reflections on Their Functions and Amyloidogenic PropertiesEfficient enzymatic cyclization of an inhibitory cystine knot-containing peptideThe chemistry and biology of theta defensins.Multifunctional αvβ6 Integrin-Specific Peptide-Pt(IV) Conjugates for Cancer Cell Targeting.Approaches to the stabilization of bioactive epitopes by grafting and peptide cyclization.Synthesis and evaluation of phosphonated N-heteroarylcarboxamides as DOXP-reductoisomerase (DXR) inhibitors.Exploring DOXP-reductoisomerase binding limits using phosphonated N-aryl and N-heteroarylcarboxamides as DXR inhibitors.The chemistry of cyclotides.Synthetic integrin-binding immune stimulators target cancer cells and prevent tumor formation.Recent Advances in Peptide-Based Approaches for Cancer Treatment.A comparative study of synthetic and semisynthetic approaches for ligating the epidermal growth factor to a bivalent scaffold.Synthetic Cancer-Targeting Innate Immune Stimulators Give Insights into Avidity Effects.Insights into the molecular flexibility of θ-defensins by NMR relaxation analysis.Advancing the Frontiers of Chemical Protein Synthesis-The 7th CPS Meeting, Haifa, Israel.Multifunctional Scaffolds for Assembling Cancer-Targeting Immune Stimulators Using Chemoselective LigationsArginine side-chain modification that occurs during copper-catalysed azide-alkyne click reactions resembles an advanced glycation end productProtein Chemistry Looking Ahead: 8th Chemical Protein Synthesis Meeting 16-19 June 2019, Berlin, GermanyRandom coil shifts of posttranslationally modified amino acidsTumor-Targeting Immune System Engagers (ISErs) Activate Human Neutrophils after Binding to Cancer CellsNative chemical ligation in protein synthesis and semi-synthesis
P50
Q27676502-2F565969-6D49-40E2-B678-96D1F2859880Q27688055-8FD483A1-12EF-4218-97B2-B7F7CEA1FDC3Q27701553-0D14784B-C969-4AE9-9350-C4CF5DD7F11BQ27704538-DA7A4226-A7C8-4612-B751-7A3598718F70Q27704653-60D08381-4D49-4D2F-A918-E92803077055Q34431648-0295984B-2E38-4EB8-80F2-D42E1046A2B3Q38695235-D9C6FE19-F9FC-4B6E-8464-F793ACF76E29Q38819655-55BA4D40-56D7-43C4-A656-FF3BCE49FC78Q39795703-DD852191-0A84-4512-9C67-D607D6C33890Q42710856-1E357FF9-705E-409D-B5D3-941C2C12D36DQ44967153-EA748472-08AB-466F-87BB-49E133A68EF4Q46783569-7154C736-45BF-4F60-A9AB-57A5B88F6FC5Q47367240-805483A2-E431-4DC5-80E0-A3C3F4743F0FQ47438485-964DCAAE-3464-48C1-BD21-2B2CAAF6C523Q48136015-6B053222-6231-46B4-AFE1-B907ABFEE07BQ50281951-D83BE457-F823-488A-8072-E8E6BAFB303EQ52652159-2A7DEB8A-D90F-4F26-8289-C0345D6D42A9Q64056464-C59BE815-431C-4F7D-9626-D24E7F0D9AD0Q87628666-A75F21F1-7F11-45FD-8B19-EE6C2D77B674Q90798396-EBB307FD-1E40-4B28-87BC-BFE026FE7CCBQ91977772-385DA636-8AF5-4E38-83A9-172A35CDF301Q92220292-622C02DC-B08B-456F-99C7-1080A0661B7DQ93002062-08A1F816-F79E-46C6-A8B2-C9A345A2417E
P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Anne C. Conibear
@ast
Anne C. Conibear
@en
Anne C. Conibear
@es
Anne C. Conibear
@nl
Anne C. Conibear
@sl
type
label
Anne C. Conibear
@ast
Anne C. Conibear
@en
Anne C. Conibear
@es
Anne C. Conibear
@nl
Anne C. Conibear
@sl
prefLabel
Anne C. Conibear
@ast
Anne C. Conibear
@en
Anne C. Conibear
@es
Anne C. Conibear
@nl
Anne C. Conibear
@sl
P1053
C-5246-2014
P106
P1153
36598269400
P21
P31
P3829
P496
0000-0002-5482-6225