Institut für Laboratoriumsmedizin, Klinische Chemie und Pathobiochemie
N-glycan analysis of recombinant L-Selectin reveals sulfated GalNAc and GalNAc-GalNAc motifs..
The transmembrane domains of L-selectin and CD44 regulate receptor cell surface positioning and leukocyte adhesion under flow.
Inhibition of selectin binding by colloidal gold with functionalized shells..
Modular synthesis of multivalent glycoarchitectures and their unique selectin binding behaviour.
Inhibition of L-selectin binding by polyacrylamide-based conjugates under defined flow conditions.
Diminished lymphocyte adhesion and alleviation of allergic responses by small-molecule- or antibody-mediated inhibition of L-selectin functions.
Optical molecular imaging of lymph nodes using a targeted vascular contrast agent.
The interaction of protein kinase C isozymes alpha, iota, and theta with the cytoplasmic domain of L-selectin is modulated by phosphorylation of the receptor.
Identification of nucleolin as a new L-selectin ligand.Dr. rer. nat. Jens Dernedde
Charité – Universitätsmedizin Berlin
Institut für Laboratoriumsmedizin, Klinische Chemie und Pathobiochemie
Campus Benjamin Franklin
Hindenburgdamm 30
D-12200 Berlin
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