about
Predictive toxicology of cobalt ferrite nanoparticles: comparative in-vitro study of different cellular models using methods of knowledge discovery from dataPredictive toxicology of cobalt nanoparticles and ions: comparative in vitro study of different cellular models using methods of knowledge discovery from data.Toward a better analysis of secreted proteins: the example of the myeloid cells secretomeTailoring nanostructured lipid carriers for the delivery of protein antigens: Physicochemical properties versus immunogenicity studies.Paramagnetic nanoparticles to track and quantify in vivo immune human therapeutic cells.B cell receptors and complement receptors target the antigen to distinct intracellular compartments.Autoactivation of human complement subcomponent C1r involves structural changes reflected in modifications of intrinsic fluorescence, circular dichroism and reactivity with monoclonal antibodies.Different in vitro exposure regimens of murine primary macrophages to silver nanoparticles induce different fates of nanoparticles and different toxicological and functional consequences.A top-down synthesis route to ultrasmall multifunctional Gd-based silica nanoparticles for theranostic applications.An interaction between CD16 and CR3 enhances iC3b binding to CR3 but is lost during differentiation of monocytes into dendritic cells.Normal differentiation and functions of mouse dendritic cells derived from RAG-deficient bone marrow progenitors.Impact of silica nanoparticle surface chemistry on protein corona formation and consequential interactions with biological cells.Anti-tumor immunotherapy via antigen delivery from a live attenuated genetically engineered Pseudomonas aeruginosa type III secretion system-based vector.CXCL-8/IL8 Produced by Diffuse Large B-cell Lymphomas Recruits Neutrophils Expressing a Proliferation-Inducing Ligand APRIL.Electronic sorting and recovery of single live cells from microlitre sized samples.The envelope of human endogenous retrovirus in neuro-inflammationCovalent binding of non-proteolysed C3 to Jurkat T cellsPrion protein activates and fixes complement directly via the classical pathway: implications for the mechanism of scrapie agent propagation in lymphoid tissueC1q binding and complement activation by prions and amyloidsOverexpression of cellular prion protein induces an antioxidant environment altering T cell development in the thymusEnhanced susceptibility of T lymphocytes to oxidative stress in the absence of the cellular prion protein
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P50
description
Forscher
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chercheur
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investigador
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researcher
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研究者
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name
C L Villiers
@ast
C L Villiers
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C L Villiers
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C L Villiers
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type
label
C L Villiers
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C L Villiers
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C L Villiers
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C L Villiers
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prefLabel
C L Villiers
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C L Villiers
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C L Villiers
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C L Villiers
@nl
P31
P496
0000-0002-6548-278X