about
Phosphorylation controls the interaction of the connexin43 C-terminal domain with tubulin and microtubulesBiochemical analysis of leishmanial and human GDP-Mannose Pyrophosphorylases and selection of inhibitors as new leads.Effect of Post-Translational Amidation on Islet Amyloid Polypeptide Conformational Ensemble: Implications for Its Aggregation Early Steps.Coarse-grained models of the proteins backbone conformational dynamics.Structure of ring-shaped Aβ₄₂ oligomers determined by conformational selection.Exploring the Alzheimer amyloid-β peptide conformational ensemble: A review of molecular dynamics approaches.Insights into the Conformational Ensemble of Human Islet Amyloid Polypeptide from Molecular Simulations.Cetuximab directly inhibits P-glycoprotein function in vitro independently of EGFR binding.Interaction of chemokine receptor CXCR4 in monomeric and dimeric state with its endogenous ligand CXCL12: coarse-grained simulations identify differences.Modeling Protein-Protein Recognition in Solution Using the Coarse-Grained Force Field SCORPION.Comparative study of structural models of Leishmania donovani and human GDP-mannose pyrophosphorylases.A semi-implicit solvent model for the simulation of peptides and proteins.Particle-Based Implicit Solvent Model for Biosimulations: Application to Proteins and Nucleic Acids Hydration.The use of 4,4,4-trifluorothreonine to stabilize extended peptide structures and mimic β-strands.Conformational Ensemble and Biological Role of the TCTP Intrinsically Disordered Region: Influence of Calcium and PhosphorylationInfluence of drug binding on DNA flexibility: a normal mode analysisA coarse-grained protein-protein potential derived from an all-atom force fieldProtein Backbone Dynamics Simulations Using Coarse-Grained Bonded Potentials and Simplified Hydrogen BondsStructure-activity relationships of β-hairpin mimics as modulators of amyloid β-peptide aggregationInvestigation into Early Steps of Actin Recognition by the Intrinsically Disordered N-WASP Domain VBinding Modes of a Glycopeptidomimetic Molecule on Aβ Protofibrils: Implication for Its Inhibition MechanismMolecular Dynamics Simulations Combined with Nuclear Magnetic Resonance and/or Small-Angle X-ray Scattering Data for Characterizing Intrinsically Disordered Protein Conformational EnsemblesStructural Characterization of N-WASP Domain V Using MD Simulations with NMR and SAXS DataGDP-Mannose Pyrophosphorylase: A Biologically Validated Target for Drug Development Against Leishmaniasis
P50
Q27678895-B1B97C37-9A90-4B10-B491-32745F1A5FF2Q33677834-648F7EAD-FE66-41FD-95F0-43FC12F47CADQ37465610-A145B044-0E94-494B-BCF9-1EC0EBD10723Q38180424-9C428800-544C-4574-83D8-7BC41768C1A9Q38379874-A8FBCC17-7D57-40CC-A7B5-45A202566A8CQ38440007-FDC98FB5-1558-42C1-8274-442B5FD6A2EEQ38807664-3ADCE056-B6D9-4CBC-859D-1E84F0D51B99Q38880372-6AF42951-CEAE-4A21-8700-EAFF9D6D3AD9Q40058610-B48ED3DC-1D53-41FB-82E2-9FCF13275BA2Q40295705-8AC677C8-3149-43A6-AB09-70AFACCF886DQ40327849-C4509403-F51A-4B8C-A798-63B175739029Q47808116-A6950409-57AE-4AB3-96EE-20DDE2829573Q51929927-3DE7D71B-F02A-4787-96B0-A15DF2C266F3Q55070006-55696FC8-17BC-4AB4-A46A-C225BE1D11DEQ57980391-AEF9D348-F820-4E91-9E80-968D102E5704Q73441787-A25FD0E8-4662-4549-A629-E4D7E26C99EAQ80578757-89C47F13-8B90-418A-924A-3E628164B245Q86820923-671A76AB-CD59-41E9-B990-83C0E4E613F7Q88883070-F3ED0294-107A-4F39-AFD6-660BBE0CBB91Q90079877-44B1D975-4799-4417-B37E-68C9603490B8Q90342947-E9627444-9766-425D-9698-FA30599BC557Q92165877-40F2521B-D84A-450F-BFD9-ADF1DA9520F9Q92409822-305B7B14-06F5-42EB-BD07-3FA6212AD3B6Q92864476-CDC2EE94-47AE-4524-B749-6712F3ADB956
P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0002-0847-2948
@en
name
Tâp Ha-Duong
@ast
Tâp Ha-Duong
@en
Tâp Ha-Duong
@nl
type
label
Tâp Ha-Duong
@ast
Tâp Ha-Duong
@en
Tâp Ha-Duong
@nl
prefLabel
Tâp Ha-Duong
@ast
Tâp Ha-Duong
@en
Tâp Ha-Duong
@nl
P106
P31
P496
0000-0002-0847-2948