Diagnosing FSGS without kidney biopsy – a novel INF2-mutation in a family with ESRD of unknown origin

por Münch, Johannes, Grohmann, Maik, Lindner, Tom H., Bergmann, Carsten, Halbritter, Jan
Publicado 2016

Atypical hemolytic uremic syndrome induced by SARS-CoV2 infection in infants with EXOSC3 mutation

por Van Quekelberghe, Chantal, Latta, Kay, Kunzmann, Steffen, Grohmann, Maik, Hansen, Matthias
Publicado 2022

A mammalianized synthetic nitroreductase gene for high-level expression

por Grohmann, Maik, Paulmann, Nils, Fleischhauer, Sebastian, Vowinckel, Jakob, Priller, Josef, Walther, Diego J
Publicado 2009

Deleterious Impact of a Novel CFH Splice Site Variant in Atypical Hemolytic Uremic Syndrome

por Schönauer, Ria, Seidel, Anna, Grohmann, Maik, Lindner, Tom H., Bergmann, Carsten, Halbritter, Jan
Publicado 2019

Restricted mobility of Dnmt1 in preimplantation embryos: implications for epigenetic reprogramming

por Grohmann, Maik, Spada, Fabio, Schermelleh, Lothar, Alenina, Natalia, Bader, Michael, Cardoso, M Cristina, Leonhardt, Heinrich
Publicado 2005

Histaminylation of glutamine residues is a novel posttranslational modification implicated in G-protein signaling

por Vowinckel, Jakob, Stahlberg, Silke, Paulmann, Nils, Bluemlein, Katharina, Grohmann, Maik, Ralser, Markus, Walther, Diego J.
Publicado 2012

Effective immunosuppressive management with belatacept and eculizumab in post-transplant aHUS due to a homozygous deletion of CFHR1/CFHR3 and the presence of CFH antibodies

por Münch, Johannes, Bachmann, Anette, Grohmann, Maik, Mayer, Christof, Kirschfink, Michael, Lindner, Tom H, Bergmann, Carsten, Halbritter, Jan
Publicado 2017

Intracellular Serotonin Modulates Insulin Secretion from Pancreatic β-Cells by Protein Serotonylation

por Paulmann, Nils, Grohmann, Maik, Voigt, Jörg-Peter, Bert, Bettina, Vowinckel, Jakob, Bader, Michael, Skelin, Maša, Jevšek, Marko, Fink, Heidrun, Rupnik, Marjan, Walther, Diego J.
Publicado 2009

The underestimated burden of monogenic kidney disease in adults waitlisted for kidney transplantation

por Schrezenmeier, Eva, Kremerskothen, Elisa, Halleck, Fabian, Staeck, Oliver, Liefeldt, Lutz, Choi, Mira, Schüler, Markus, Weber, Ulrike, Bachmann, Nadine, Grohmann, Maik, Wagner, Timo, Budde, Klemens, Bergmann, Carsten
Publicado 2021

Correction to: The underestimated burden of monogenic kidney disease in adults waitlisted for kidney transplantation

por Schrezenmeier, Eva, Kremerskothen, Elisa, Halleck, Fabian, Staeck, Oliver, Liefeldt, Lutz, Choi, Mira, Schüler, Markus, Weber, Ulrike, Bachmann, Nadine, Grohmann, Maik, Wagner, Timo, Budde, Klemens, Bergmann, Carsten
Publicado 2021

Alternative Splicing and Extensive RNA Editing of Human TPH2 Transcripts

por Grohmann, Maik, Hammer, Paul, Walther, Maria, Paulmann, Nils, Büttner, Andreas, Eisenmenger, Wolfgang, Baghai, Thomas C., Schüle, Cornelius, Rupprecht, Rainer, Bader, Michael, Bondy, Brigitta, Zill, Peter, Priller, Josef, Walther, Diego J.
Publicado 2010

Loss of the collagen IV modifier prolyl 3-hydroxylase 2 causes thin basement membrane nephropathy

por Aypek, Hande, Krisp, Christoph, Lu, Shun, Liu, Shuya, Kylies, Dominik, Kretz, Oliver, Wu, Guochao, Moritz, Manuela, Amann, Kerstin, Benz, Kerstin, Tong, Ping, Hu, Zheng-mao, Alsulaiman, Sulaiman M., Khan, Arif O., Grohmann, Maik, Wagner, Timo, Müller-Deile, Janina, Schlüter, Hartmut, Puelles, Victor G., Bergmann, Carsten, Huber, Tobias B., Grahammer, Florian
Publicado 2022

Collagen IV(α345) dysfunction in glomerular basement membrane diseases. I. Discovery of a COL4A3 variant in familial Goodpasture’s and Alport diseases

por Pokidysheva, Elena N., Seeger, Harald, Pedchenko, Vadim, Chetyrkin, Sergei, Bergmann, Carsten, Abrahamson, Dale, Cui, Zhao Wei, Delpire, Eric, Fervenza, Fernando C., Fidler, Aaron L., Fogo, Agnes B., Gaspert, Ariana, Grohmann, Maik, Gross, Oliver, Haddad, George, Harris, Raymond C., Kashtan, Clifford, Kitching, A. Richard, Lorenzen, Johan M., McAdoo, Stephen, Pusey, Charles D., Segelmark, Marten, Simmons, Alicia, Voziyan, Paul A., Wagner, Timo, Wüthrich, Rudolf P., Zhao, Ming-Hui, Boudko, Sergei P., Kistler, Andreas D., Hudson, Billy G.
Publicado 2021

Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function

por Bedin, Mathilda, Boyer, Olivia, Servais, Aude, Li, Yong, Villoing-Gaudé, Laure, Tête, Marie-Josephe, Cambier, Alexandra, Hogan, Julien, Baudouin, Veronique, Krid, Saoussen, Bensman, Albert, Lammens, Florie, Louillet, Ferielle, Ranchin, Bruno, Vigneau, Cecile, Bouteau, Iseline, Isnard-Bagnis, Corinne, Mache, Christoph J., Schäfer, Tobias, Pape, Lars, Gödel, Markus, Huber, Tobias B., Benz, Marcus, Klaus, Günter, Hansen, Matthias, Latta, Kay, Gribouval, Olivier, Morinière, Vincent, Tournant, Carole, Grohmann, Maik, Kuhn, Elisa, Wagner, Timo, Bole-Feysot, Christine, Jabot-Hanin, Fabienne, Nitschké, Patrick, Ahluwalia, Tarunveer S., Köttgen, Anna, Andersen, Christian Brix Folsted, Bergmann, Carsten, Antignac, Corinne, Simons, Matias
Publicado 2022