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Complement factor H and hemolytic uremic syndrome.
Zipfel PF, Skerka C, Caprioli J, Manuelian T, Neumann HH, Noris M, Remuzzi G. Zipfel PF, et al. Among authors: skerka c. Int Immunopharmacol. 2001 Mar;1(3):461-8. doi: 10.1016/s1567-5769(00)00047-3. Int Immunopharmacol. 2001. PMID: 11367530 Review.
Factor H family proteins: on complement, microbes and human diseases.
Zipfel PF, Skerka C, Hellwage J, Jokiranta ST, Meri S, Brade V, Kraiczy P, Noris M, Remuzzi G. Zipfel PF, et al. Among authors: skerka c. Biochem Soc Trans. 2002 Nov;30(Pt 6):971-8. doi: 10.1042/bst0300971. Biochem Soc Trans. 2002. PMID: 12440956 Review.
De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome.
Heinen S, Sanchez-Corral P, Jackson MS, Strain L, Goodship JA, Kemp EJ, Skerka C, Jokiranta TS, Meyers K, Wagner E, Robitaille P, Esparza-Gordillo J, Rodriguez de Cordoba S, Zipfel PF, Goodship TH. Heinen S, et al. Among authors: skerka c. Hum Mutat. 2006 Mar;27(3):292-3. doi: 10.1002/humu.9408. Hum Mutat. 2006. PMID: 16470555
Complement dysfunction in hemolytic uremic syndrome.
Zipfel PF, Skerka C. Zipfel PF, et al. Among authors: skerka c. Curr Opin Rheumatol. 2006 Sep;18(5):548-55. doi: 10.1097/01.bor.0000240370.47336.ae. Curr Opin Rheumatol. 2006. PMID: 16896298 Review.
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