Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and Bronchiectasis

Dougherty, Gerard W., Ostrowski, Lawrence E., Nöthe-Menchen, Tabea, Raidt, Johanna Felicitas, Schramm, Andre, Olbrich, Heike, Yin, Weining, Sears, Patrick R., Dang, Hong, Smith, Amanda J., Beule, Achim Georg, Hjeij, Rim, Rutjes, Niels, Haarman, Eric G, Maas, Saskia M., Ferkol, Thomas W., Noone, Peadar G., Olivier, Kenneth N., Bracht, Diana C., Barbry, Pascal, Zaragosi, Laure-Emmanuelle, Fierville, Morgane, Kliesch, Sabine, Wohlgemuth, Kai, König, Julia, George, Sebastian, Loges, Niki T., Ceppe, Agathe, Markovetz, Matthew R., Luo, Hong, Guo, Ting, Rizk, Hoda, Eldesoky, Tarek, Dahlke, Katrin, Boldt, Karsten, Ueffing, Marius, Hill, David B., Pang, Yuan-Ping, Knowles, Michael R., Zariwala, Maimoona A., Omran, Heymut
2024

Transskriptomische Analyse der postnatalen Entwicklung der Rattenretina in Bezug auf den kritischen Zeitpunkt der Augenöffnung

Schröer, Uwe
2006

A PQS-Cleaving Quorum Quenching Enzyme Targets Extracellular Membrane Vesicles of Pseudomonas aeruginosa

Arranz San Martín, Alba, Drees, Steffen Lorenz, Fetzner, Susanne
2022

MAPT genotype-dependent mitochondrial aberration and ROS production trigger dysfunction and death in cortical neurons of patients with hereditary FTLD

Korn, Lisanne, Speicher, Anna M., Schroeter, Christina Barbara, Gola, Lukas, Kaehne, Thilo, Engler, Alexander, Disse, Paul, Fernandez-Orth, Juncal, Csatári, Júlia, Naumann, Michael, Seebohm, Guiscard Friedrich Aldous, Meuth, Sven, Schöler, Hans Robert, Wiendl, Heinz, Kovać, Stjepana, Pawlowski, Matthias
2022