A Closer Look on the Polyhydroxybutyrate- (PHB-) Negative Phenotype of Ralstonia eutropha PHB-4

Raberg, Matthias, Voigt, Birgit, Hecker, Michael, Steinbüchel, Alexander
2014

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

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