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G. Ulrich Nienhaus

Researcher at Karlsruhe Institute of Technology

Publications -  269
Citations -  19651

G. Ulrich Nienhaus is an academic researcher from Karlsruhe Institute of Technology. The author has contributed to research in topics: Green fluorescent protein & Ligand (biochemistry). The author has an hindex of 74, co-authored 259 publications receiving 17790 citations. Previous affiliations of G. Ulrich Nienhaus include University of Illinois at Urbana–Champaign & Russian Academy of Sciences.

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Ultra-small fluorescent metal nanoclusters: Synthesis and biological applications

TL;DR: In this article, the authors summarize synthesis strategies of water-soluble fluorescent metal nanoclusters and their optical properties, highlight recent advances in their application for ultrasensitive biological detection and fluorescent biological imaging, and finally discuss current challenges for their potential biomedical applications.
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A quantitative fluorescence study of protein monolayer formation on colloidal nanoparticles.

TL;DR: In this article, the authors quantitatively analyzed the adsorption of human serum albumin onto small polymer-coated FePt and CdSe/ZnS nanoparticles by using fluorescence correlation spectroscopy.
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EosFP, a fluorescent marker protein with UV-inducible green-to-red fluorescence conversion

TL;DR: A gene encoding a fluorescent protein from the stony coral Lobophyllia hemprichii has been cloned in Escherichia coli and characterized by biochemical and biophysical methods and is found to be tetrameric, with strong Forster resonance coupling among the individual fluorophores.
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Surface Functionalization of Nanoparticles with Polyethylene Glycol: Effects on Protein Adsorption and Cellular Uptake

TL;DR: Even though the P EG coatings did not completely prevent protein adsorption, the PEGylated NPs still displayed a pronounced reduction of cellular uptake with respect to bare NPs, which is to be expected if the adsorbed proteins are not exposed on the NP surface.
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Differential Uptake of Functionalized Polystyrene Nanoparticles by Human Macrophages and a Monocytic Cell Line

TL;DR: The data show that the amount of internalized nanoparticles, the uptake kinetics, and its mechanism may differ considerably between primary cells and a related tumor cell line, whether differentiated or not, and that particle uptake by these cells is critically dependent on particle opsonization by serum proteins.