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Dick Hoekstra

Researcher at University Medical Center Groningen

Publications -  280
Citations -  19674

Dick Hoekstra is an academic researcher from University Medical Center Groningen. The author has contributed to research in topics: Vesicle & Lipid bilayer fusion. The author has an hindex of 69, co-authored 280 publications receiving 18789 citations. Previous affiliations of Dick Hoekstra include University of Groningen.

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Kinetics of intermixing of lipids and mixing of aqueous contents during vesicle fusion

TL;DR: Under conditions where leakage of vesicle contents during fusion is limited, both fusion assays accurately reflect the occurrence of this process, thus indicating the usefulness of these assays as reliable, complementary tools in the study of fusion of (model) membranes.
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The influence of physicochemical parameters on the efficacy of non-viral DNA transfection complexes: a comparative study.

TL;DR: Transfection efficiency seems to require a positive or neutral zeta potential, which is depending on size, e.g., is higher for smaller particles, and requires a vector that is stable in serum.
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Probe transfer with and without membrane fusion in a fluorescence fusion assay

TL;DR: The kinetics of the R18-labeled lipid mixing were compared to those obtained with an assay in which the fusion-monitoring probe, eosin-maleimide, was attached to the viral surface proteins and the increase in R18 fluorescence was evaluated in terms of the different processes that in principle may contribute to this increase.
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Novel biodegradable pyridinium amphiphiles for gene delivery

TL;DR: Biodegradable synthetic cationic pyridinium-based amphiphiles (SAINTs) prove to be promising non-viral carrier systems for delivery of DNA into eukaryotic cells.
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Differential effects of TNF (TNFSF2) and IFN-γ on intestinal epithelial cell morphogenesis and barrier function in three-dimensional culture.

TL;DR: This study provides an optimized 3D model system for the integrated analysis of (real-time) intestinal epithelial paracellular permeability and morphogenesis, and reveals apoptosis as a pivotal mechanism underlying the enhanced permeable and altered morphogenesis in response to TNF, but not IFNγ.