2022 - Research.com Microbiology in Germany Leader Award
Peter F. Zipfel mostly deals with Factor H, Complement system, Alternative complement pathway, Microbiology and Molecular biology. His Factor H study is associated with Immunology. The concepts of his Immunology study are interwoven with issues in Genetics and Gene.
His studies deal with areas such as Platelet, Innate immune system and Endocrinology as well as Complement system. As part of the same scientific family, Peter F. Zipfel usually focuses on Alternative complement pathway, concentrating on Biochemistry and intersecting with Candida albicans. His Microbiology research integrates issues from Virulence factor, Borrelia burgdorferi, Immune system and Binding site.
The scientist’s investigation covers issues in Factor H, Complement system, Microbiology, Immunology and Alternative complement pathway. His Factor H study integrates concerns from other disciplines, such as Complement factor I, Molecular biology and Cell biology. As a part of the same scientific family, he mostly works in the field of Cell biology, focusing on Complement and, on occasion, Regulator.
In most of his Complement system studies, his work intersects topics such as Plasma protein binding. His research integrates issues of Plasmin, Innate immune system, Immune system and Borrelia burgdorferi in his study of Microbiology. The Immunology study combines topics in areas such as Internal medicine and Disease.
His primary areas of investigation include Complement system, Immune system, Microbiology, Immunology and Cell biology. His research related to Factor H, Alternative complement pathway, Complement inhibitor and Complement factor I might be considered part of Complement system. Peter F. Zipfel studies Factor H, focusing on CFHR5 in particular.
His Immune system study combines topics from a wide range of disciplines, such as Virology, Gene, Borrelia miyamotoi and Candida albicans. The study incorporates disciplines such as Receptor, Plasma protein binding, Vitronectin and Plasmin in addition to Microbiology. His work in Immunology tackles topics such as Glomerulopathy which are related to areas like Transplantation, Membranoproliferative glomerulonephritis, Atypical hemolytic uremic syndrome and Vasculitis.
His primary areas of study are Complement system, Immunology, Microbiology, Innate immune system and Alternative complement pathway. His Complement system research is multidisciplinary, incorporating elements of Molecular biology and Microglia. His work carried out in the field of Immunology brings together such families of science as Albuminuria and Glomerulopathy.
His biological study spans a wide range of topics, including Extracellular and Plasmin. His Alternative complement pathway research is multidisciplinary, relying on both Recombinant DNA, Glycosylation, Glycoprotein, Disease and Pharmacology. His Factor H research includes themes of Complement factor I, Classical complement pathway and Virology.
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Complement Resistance of Borrelia burgdorferi Correlates with the Expression of BbCRASP-1, a Novel Linear Plasmid-encoded Surface Protein That Interacts with Human Factor H and FHL-1 and Is Unrelated to Erp Proteins
Peter Kraiczy;Jens Hellwage;Christine Skerka;Heiko Becker.
Journal of Biological Chemistry (2004)
Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries
H P H Neumann;M Salzmann;B Bohnert-Iwan;T Mannuelian.
Journal of Medical Genetics (2003)
Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease)
Maria Asuncion Abrera-Abeleda;Carla Nishimura;Jenna L.H. Smith;Sanjjev Sethi.
Journal of Medical Genetics (2005)
Complement and diseases: defective alternative pathway control results in kidney and eye diseases.
Peter F. Zipfel;Stefan Heinen;Mihály Józsi;Christine Skerka.
Molecular Immunology (2006)
Immune evasion of the human pathogen Pseudomonas aeruginosa: elongation factor Tuf is a factor H and plasminogen binding protein.
Anja Kunert;Josephine Losse;Christin Gruszin;Michael Hühn.
Journal of Immunology (2007)
Regulation of Complement Activation by C-Reactive Protein: Targeting the Complement Inhibitory Activity of Factor H by an Interaction with Short Consensus Repeat Domains 7 and 8–11
Jarva H;Jokiranta Ts;Hellwage J;Zipfel Pf.
Journal of Immunology (1999)
Mitogenic activation of human T cells induces two closely related genes which share structural similarities with a new family of secreted factors.
Zipfel Pf;Balke J;Irving Sg;Kelly K.
Journal of Immunology (1989)
Anti–factor H autoantibodies block C-terminal recognition function of factor H in hemolytic uremic syndrome
Mihály Józsi;Stefanie Strobel;Hans-Martin Dahse;Wei-shih Liu.
The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural models.
Rebecca E. Saunders;Cynthia Abarrategui-Garrido;Véronique Frémeaux-Bacchi;Elena Goicoechea de Jorge.
Human Mutation (2007)
Nephritogenic lambda light chain dimer: a unique human miniautoantibody against complement factor H.
Jokiranta Ts;Solomon A;Pangburn Mk;Zipfel Pf.
Journal of Immunology (1999)
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