Development of a DNA-labeling system for array-based comparative genomic hybridization von Lieu, Pauline T, Jozsi, Peter, Gilles, Patrick, Peterson, Todd

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Factor H family proteins and human diseases von Józsi, Mihály, Zipfel, Peter F

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Functional analyses indicate a pathogenic role of factor H autoantibodies in atypical haemolytic uraemic syndrome von Strobel, Stefanie, Hoyer, Peter F., Mache, Christoph J., Sulyok, Endre, Liu, Wei-shih, Richter, Heiko, Oppermann, Martin, Zipfel, Peter F., Józsi, Mihály

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C3 glomerulopathy — understanding a rare complement-driven renal disease von Smith, Richard J. H., Appel, Gerald B., Blom, Anna M., Cook, H. Terence, D’Agati, Vivette D, Fakhouri, Fadi, Fremeaux-Bacchi, Véronique, Józsi, Mihály, Kavanagh, David, Lambris, John D., Noris, Marina, Pickering, Matthew C., Remuzzi, Giuseppe, de Córdoba, Santiago Rodriguez, Sethi, Sanjeev, Van der Vlag, Johan, Zipfel, Peter F., Nester, Carla M.

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Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome von Manuelian, Tamara, Hellwage, Jens, Meri, Seppo, Caprioli, Jessica, Noris, Marina, Heinen, Stefan, Jozsi, Mihaly, Neumann, Hartmut P H, Remuzzi, Giuseppe, Zipfel, Peter F

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Factor H and Factor H-Related Protein 1 Bind to Human Neutrophils via Complement Receptor 3, Mediate Attachment to Candida albicans, and Enhance Neutrophil Antimicrobial Activity von Losse, Josephine, Zipfel, Peter F, Jozsi, Mihaly

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Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome von Manuelian, T, Hellwage, J, Meri, S, Caprioli, J, Noris, M, Heinen, S, Jozsi, M, Neumann, HPH, Remuzzi, G, Zipfel, P F

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Large-Scale Plasma Proteome Epitome Profiling is an Efficient Tool for the Discovery of Cancer Biomarkers von Lazar, Jozsef, Antal-Szalmas, Peter, Kurucz, Istvan, Ferenczi, Annamaria, Jozsi, Mihaly, Tornyi, Ilona, Muller, Monika, Fekete, Janos Tibor, Lamont, John, FitzGerald, Peter, Gall-Debreceni, Anna, Kadas, Janos, Vida, Andras, Tardieu, Nadege, Kieffer, Yann, Jullien, Anne, Guergova-Kuras, Mariana, Hempel, William, Kovacs, Andras, Kardos, Tamas, Bittner, Nora, Csanky, Eszter, Szilasi, Maria, Losonczy, Gyorgy, Szondy, Klara, Galffy, Gabriella, Csada, Edit, Szalontai, Klara, Somfay, Attila, Malka, David, Cottu, Paul, Bogos, Krisztina, Takacs, Laszlo

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Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency von Józsi, Mihály, Licht, Christoph, Strobel, Stefanie, Zipfel, Svante L.H., Richter, Heiko, Heinen, Stefan, Zipfel, Peter F., Skerka, Christine

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Anti–factor H autoantibodies block C-terminal recognition function of factor H in hemolytic uremic syndrome von Józsi, Mihály, Strobel, Stefanie, Dahse, Hans-Martin, Liu, Wei-shih, Hoyer, Peter F., Oppermann, Martin, Skerka, Christine, Zipfel, Peter F.

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SARS-CoV-2 Nucleocapsid Protein Is Not Responsible for Over-Activation of Complement Lectin Pathway von Kocsis, Andrea, Bartus, Dalma, Hirsch, Edit, Józsi, Mihály, Hajdú, István, Dobó, József, Balczer, Júlia, Pál, Gábor, Gál, Péter

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Ecotin, a microbial inhibitor of serine proteases, blocks multiple complement dependent and independent microbicidal activities of human serum von Nagy, Zoltán Attila, Szakács, Dávid, Boros, Eszter, Héja, Dávid, Vígh, Eszter, Sándor, Noémi, Józsi, Mihály, Oroszlán, Gábor, Dobó, József, Gál, Péter, Pál, Gábor

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Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome von Zipfel, Peter F, Edey, Matthew, Heinen, Stefan, Józsi, Mihály, Richter, Heiko, Misselwitz, Joachim, Hoppe, Bernd, Routledge, Danny, Strain, Lisa, Hughes, Anne E, Goodship, Judith A, Licht, Christoph, Goodship, Timothy H J, Skerka, Christine

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Binding of Complement Factor H to Endothelial Cells Is Mediated by the Carboxy-Terminal Glycosaminoglycan Binding Site von Jokiranta, T. Sakari, Cheng, Zhu-Zhu, Seeberger, Harald, Jòzsi, Mihály, Heinen, Stefan, Noris, Marina, Remuzzi, Giuseppe, Ormsby, Rebecca, Gordon, David L., Meri, Seppo, Hellwage, Jens, Zipfel, Peter F.

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Autoantibodies in haemolytic uraemic syndrome (HUS) von Skerka, Christine, Józsi, Mihály, Zipfel, Peter F., Dragon-Durey, Marie-Agnes, Fremeaux-Bacchi, Veronique

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Complement and diseases: Defective alternative pathway control results in kidney and eye diseases von Zipfel, Peter F., Heinen, Stefan, Józsi, Mihály, Skerka, Christine

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Secreted aspartic protease 2 of Candida albicans inactivates factor H and the macrophage factor H-receptors CR3 (CD11b/CD18) and CR4 (CD11c/CD18) von Svoboda, Eliška, Schneider, Andrea E, Sándor, Noémi, Lermann, Ulrich, Staib, Peter, Kremlitzka, Mariann, Bajtay, Zsuzsa, Barz, Dagmar, Erdei, Anna, Józsi, Mihály

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Differential interaction of the two related fungal species Candida albicans and Candida dubliniensis with human neutrophils von Svobodová, Eliska, Staib, Peter, Losse, Josephine, Hennicke, Florian, Barz, Dagmar, Józsi, Mihály

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The C-terminus of complement factor H is essential for host cell protection von Józsi, Mihály, Oppermann, Martin, Lambris, John D., Zipfel, Peter F.

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Autoimmune forms of thrombotic micorangiopathy and membranoproliferative glomerulonephritis: Indications for a disease spectrum and common pathogenic principles von Skerka, Christine, Licht, Christoph, Mengel, Michael, Uzonyi, Barbara, Strobel, Stefanie, Zipfel, Peter F., Józsi, Mihály

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