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

Immunoadsorption versus double-dose methylprednisolone in refractory multiple sclerosis relapses

Pfeuffer, Steffen, Rolfes, Leoni, Wirth, Timo, Steffen, Falk, Pawlitzki, Marc, Schulte-Mecklenbeck, Andreas, Gross, Catharina C., Brand, Marcus, Bittner, Stefan, Ruck, Tobias, Klotz, Luisa Hildegard, Wiendl, Heinz, Meuth, Sven
2022

Spezifische Tumortherapie durch Rezeptorvermittelte RNA Interferenz

Appel, Neele
2017

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