Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ina Löschmann"'
Autor:
Sarah Irmscher, Svante L. H. Zipfel, Luke D. Halder, Lia Ivanov, Andres Gonzalez-Delgado, Christoph Waldeyer, Moritz Seiffert, Fabian J. Brunner, Monika von der Heide, Ina Löschmann, Sonia Wulf, Darina Czamara, Nikolina Papac-Milicevic, Olaf Strauß, Stefan Lorkowski, Hermann Reichenspurner, Michael V. Holers, Nirmal K. Banda, Tania Zeller, Elisabeth B. Binder, Christoph J. Binder, Thorsten Wiech, Peter F. Zipfel, Christine Skerka
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
Abstract Atherosclerotic cardiovascular disease (ACVD) is a lipid-driven inflammatory disease and one of the leading causes of death worldwide. Lipid deposits in the arterial wall lead to the formation of plaques that involve lipid oxidation, cellula
Externí odkaz:
https://doaj.org/article/f4fef222f3624b56b6f873bb7fc7bb7a
Autor:
Fei Zhao, Sara Afonso, Susanne Lindner, Andrea Hartmann, Ina Löschmann, Bo Nilsson, Kristina N. Ekdahl, Lutz T. Weber, Sandra Habbig, Gesa Schalk, Michael Kirschfink, Peter F. Zipfel, Christine Skerka
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
C3 glomerulopathy (C3G) is a severe kidney disease, which is caused by defective regulation of the alternative complement pathway. Disease pathogenesis is heterogeneous and is caused by both autoimmune and genetic factors. Here we characterized IgG a
Externí odkaz:
https://doaj.org/article/5d550f1fe1af4ecaa888ba08162e924f
Autor:
Sandra Habbig, Gesa Schalk, Kristina Nilsson Ekdahl, S Lindner, Christine Skerka, Fei Zhao, Ina Löschmann, Sara Afonso, Andrea Hartmann, Bo Nilsson, Peter F. Zipfel, Michael Kirschfink, Lutz T. Weber
Publikováno v:
Frontiers in Immunology
Frontiers in Immunology, Vol 10 (2019)
Frontiers in Immunology, Vol 10 (2019)
C3 glomerulopathy (C3G) is a severe kidney disease, which is caused by defective regulation of the alternative complement pathway. Disease pathogenesis is heterogeneous and is caused by both autoimmune and genetic factors. Here we characterized IgG a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e11f6cd5e9ed6d21c5e752cb288c0a43
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-387940
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-387940
Autor:
Christine Skerka, Peter F. Zipfel, Anna Erdei, Mihály Józsi, Heiko Richter, Friedrich Buck, Ulrike Beisiegel, Ina Löschmann
Publikováno v:
European Journal of Human Genetics. 13:321-329
We describe a new member of the human Factor H protein family, termed Factor H-related protein 4A (FHR-4A). The corresponding cDNA sequence was isolated and encodes a secreted protein of 559 amino acids, with a predicted molecular weight of 63.2 kDa.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::681e12a4261066a195e0951ceb36d3a3
https://doi.org/10.1038/sj.ejhg.5201324
https://doi.org/10.1038/sj.ejhg.5201324
Autor:
Christoph Licht, Stephen J. Perkins, Ina Löschmann, Michael Kirschfink, Bernd Hoppe, Rebecca E. Saunders, Christine Skerka, Mihály Józsi, Peter F. Zipfel, Ruediger Waldherr, Stefan Heinen
Publikováno v:
Kidney international. 70(1)
We report a novel pathomechanism for membranoproliferative glomerulonephritis type II (MPGN II) caused by a mutant Factor H protein expressed in the plasma. Genetic analyses of two patients revealed deletion of a single Lys residue (K224) located wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b092710a9c0c2cb7f48143fd33bb8f95
https://pubmed.ncbi.nlm.nih.gov/16810287
https://pubmed.ncbi.nlm.nih.gov/16810287