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Serge Muyldermans

Researcher at Vrije Universiteit Brussel

Publications -  323
Citations -  30516

Serge Muyldermans is an academic researcher from Vrije Universiteit Brussel. The author has contributed to research in topics: Single-domain antibody & Antibody. The author has an hindex of 80, co-authored 305 publications receiving 26561 citations. Previous affiliations of Serge Muyldermans include Dalian University of Technology & Université libre de Bruxelles.

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Targeted alpha therapy using short-lived alpha-particles and the promise of nanobodies as targeting vehicle

TL;DR: It is argued that the nanobodies’ pharmacokinetic properties match perfectly with the interesting decay properties of the short-lived α-particle emitting radionuclides Astatine-211 and Bismuth-213 and offer an interesting treatment option particularly for micrometastatic cancer and residual disease.
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Localization, mechanism and reduction of renal retention of technetium-99m labeled epidermal growth factor receptor-specific nanobody in mice.

TL;DR: Megalin contributes to the renal accumulation of (99m)Tc-7C12 and the combined effect of gelofusine and lysine was the most effective, namely a reduction of renal retention and improved tumor uptake.
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In Vitro Analysis and In Vivo Tumor Targeting of a Humanized, Grafted Nanobody in Mice Using Pinhole SPECT/Micro-CT

TL;DR: This study shows the potency of antigen-binding loop-grafting to efficiently generate humanized Nanobodies that retain their targeting capacities for noninvasive in vivo imaging of tumors.
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A bispecific nanobody to provide full protection against lethal scorpion envenoming

TL;DR: To ameliorate the current 100‐kDa horse plasma antivenom serum (PAS)‐derived Fab′2 to more quickly reach the highly diffusible scorpion toxins, the designed bispecific NbF12‐10 against AahI′/AahII toxins succeeded in neutralizing 5 LD50.
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Reduced global cooperativity is a common feature underlying the amyloidogenicity of pathogenic lysozyme mutations.

TL;DR: Results indicate that the reduction in global cooperativity, and the associated ability to populate transiently a specific, partly unfolded intermediate state under physiologically relevant conditions, is a common feature underlying the behaviour of these two pathogenic mutations.