Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Hannes U Eberhardt"'
Autor:
Hannes U Eberhardt, Denise Buhlmann, Peter Hortschansky, Qian Chen, Sascha Böhm, Markus J Kemper, Reinhard Wallich, Andrea Hartmann, Teresia Hallström, Peter F Zipfel, Christine Skerka
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e78617 (2013)
Mutations and deletions within the human CFHR gene cluster on chromosome 1 are associated with diseases, such as dense deposit disease, CFHR nephropathy or age-related macular degeneration. Resulting mutant CFHR proteins can affect complement regulat
Externí odkaz:
https://doaj.org/article/0a3e82dd6e944352ab29effbc719de8a
Autor:
Denise Buhlmann, Hannes U. Eberhardt, Marc Thilo Figge, Peter F. Zipfel, Christine Skerka, Anna Medyukhina, Wolfgang M. Prodinger
Publikováno v:
The Journal of Immunology. 197:620-629
The autoimmune renal disease deficient for complement factor H–related (CFHR) genes and autoantibody-positive form of hemolytic uremic syndrome is characterized by the presence of autoantibodies specific for the central complement regulator, factor
Autor:
Christian Hugo, Christine Skerka, Hannes U. Eberhardt, Kerstin Amann, Peter F. Zipfel, Michael Kirschfink, Barbara Uzonyi, Timothy H.J. Goodship, Qian Chen, Michael S. Wiesener, Maike Buettner, Andrea Hartmann
Publikováno v:
Journal of Clinical Investigation; Vol 124
The renal disorder C3 glomerulopathy with dense deposit disease (C3G-DDD) pattern results from complement dysfunction and primarily affects children and young adults. There is no effective treatment, and patients often progress to end-stage renal fai
Autor:
Lin Zhou, Paul N. Barlow, Takayuki Hamano, Yuko Kimura, Kenneth S. K. Tung, Sayaka Sato, Hannes U. Eberhardt, Peter F. Zipfel, Damodar Gullipalli, C. Skerka, Allison M. Lesher, Wen-Chao Song, Takashi Miwa, Andrew P. Herbert
Publikováno v:
Journal of the American Society of Nephrology. 24:53-65
Factor H (fH) and properdin both modulate complement; however, fH inhibits activation, and properdin promotes activation of the alternative pathway of complement. Mutations in fH associate with several human kidney diseases, but whether inhibiting pr
Autor:
Reinhard Wallich, Qian Chen, Hannes U. Eberhardt, Peter F. Zipfel, Teresia Hallström, Andrea Hartmann, Markus J. Kemper, Denise Buhlmann, Peter Hortschansky, Christine Skerka, Sascha Böhm
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e78617 (2013)
PLoS ONE
PLoS ONE
Mutations and deletions within the human CFHR gene cluster on chromosome 1 are associated with diseases, such as dense deposit disease, CFHR nephropathy or age-related macular degeneration. Resulting mutant CFHR proteins can affect complement regulat
Autor:
Brian Stevenson, Hannes U. Eberhardt, Corinna Siegel, Peter F. Zipfel, Barbara Uzonyi, Peter Kraiczy, Teresia Hallström, Michael Karas, Christine Skerka, Tobias Beckhaus, Reinhard Wallich
Publikováno v:
PLoS ONE
PLoS ONE, Vol 5, Iss 10, p e13519 (2010)
PLoS ONE, Vol 5, Iss 10, p e13519 (2010)
Background: One virulence property of Borrelia burgdorferi is its resistance to innate immunity, in particular to complement-mediated killing. Serum-resistant B. burgdorferi express up to five distinct complement regulator-acquiring surface proteins
Publikováno v:
Molecular Immunology. 56:312-313
Autor:
Qian Chen, Christine Skerka, Christian Hugo, Michael Wiesener, Andrea Hartmann, Peter F. Zipfel, Hannes U. Eberhardt
Publikováno v:
Immunobiology. 217:1131-1132
Autor:
Michael S. Wiesener, Christian Hugo, Kerstin Amann, C. Skerka, Qian Chen, Michael Kirschfink, Peter F. Zipfel, Andrea Hartmann, Hannes U. Eberhardt, Timothy H.J. Goodship, Maike Buettner
Publikováno v:
Molecular Immunology. 56:248
Autor:
Qian Chen, Teresia Hallström, Andrea Hartmann, Peter F. Zipfel, Hannes U. Eberhardt, Christine Skerka
Publikováno v:
Immunobiology. 217:1143