High-Throughput Profiling of Colorectal Cancer Liver Metastases Reveals Intra- and Inter-Patient Heterogeneity in the EGFR and WNT Pathways Associated with Clinical Outcome

Menck, Kerstin, Wlochowitz, Darius, Wachter, Astrid, Conradi, Lena-Christin, Wolff, Alexander, Scheel, Andreas, Korf, Ulrike, Wiemann, Stefan, Schildhaus, Hans-Ulrich, Bohnenberger, Hanibal, Wingender, Edgar, Pukrop, Tobias, Homayounfar, Kia, Beissbarth, Tim, Bleckmann, Annalen
2022

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

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

Diagnosing contaminations of Echis venom pools

König, Simone, Berg, Anna Maria, Aiyelaagbe, Olapeju, Adeyi, Akindele, Abiola, Julius
Veröffentlicht in: Mercator Journal of Biomolecular Analysis
2024

Life cycle adapted upstream open reading frames (uORFs) in 'Trypanosoma congolense': A post-transcriptional approach to accurate gene regulation

Fervers, Philipp Christopher, Fervers, Florian, Makałowski, Wojciech, Jąkalski, Marcin
2018

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

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

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

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