Do complement factor H 402Y and C7 M allotypes predispose to (typical) haemolytic uraemic syndrome?
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A. Mellmann | H. Karch | R. Würzner | S. Neururer | D. Orth | K. Poolpol | B. Gadner
[1] H. Jarva,et al. Complement factor H allotype 402H is associated with increased C3b opsonization and phagocytosis of Streptococcus pyogenes , 2012 .
[2] K. Budde,et al. Epidemiological Approach to Identifying Genetic Predispositions for Atypical Hemolytic Uremic Syndrome , 2010, Annals of human genetics.
[3] J. Thurman,et al. Alternative pathway of complement in children with diarrhea-associated hemolytic uremic syndrome. , 2009, Clinical journal of the American Society of Nephrology : CJASN.
[4] H. Karch,et al. Shiga Toxin Activates Complement and Binds Factor H: Evidence for an Active Role of Complement in Hemolytic Uremic Syndrome1 , 2009, The Journal of Immunology.
[5] P. Picotti,et al. C7 is expressed on endothelial cells as a trap for the assembling terminal complement complex and may exert anti-inflammatory function. , 2009, Blood.
[6] P. Zipfel,et al. Autoantibodies in haemolytic uraemic syndrome (HUS) , 2009, Thrombosis and Haemostasis.
[7] L. Zimmerhackl,et al. Treatment and outcome of Shiga-toxin-associated hemolytic uremic syndrome (HUS) , 2008, Pediatric Nephrology.
[8] S. D. de Córdoba,et al. Translational Mini‐Review Series on Complement Factor H: Genetics and disease associations of human complement factor H , 2007, Clinical and experimental immunology.
[9] M. Dierich,et al. The Shiga toxin genotype rather than the amount of Shiga toxin or the cytotoxicity of Shiga toxin in vitro correlates with the appearance of the hemolytic uremic syndrome. , 2007, Diagnostic microbiology and infectious disease.
[10] M. Oppermann,et al. Anti factor H autoantibodies block C-terminal recognition function of factor H in hemolytic uremic syndrome. , 2007, Blood.
[11] J. Atkinson,et al. Complement factor H and the hemolytic uremic syndrome , 2007, The Journal of experimental medicine.
[12] G. Remuzzi,et al. 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 , 2007, Human mutation.
[13] Ammarin Thakkinstian,et al. Systematic review and meta-analysis of the association between complementary factor H Y402H polymorphisms and age-related macular degeneration , 2006 .
[14] H. Karch,et al. Enterohaemorrhagic Escherichia coli in human medicine. , 2005, International journal of medical microbiology : IJMM.
[15] R. T. Smith,et al. A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[16] J. Gilbert,et al. Complement Factor H Variant Increases the Risk of Age-Related Macular Degeneration , 2005, Science.
[17] A. Edwards,et al. Complement Factor H Polymorphism and Age-Related Macular Degeneration , 2005, Science.
[18] J. Ott,et al. Complement Factor H Polymorphism in Age-Related Macular Degeneration , 2005, Science.
[19] W. Fridman,et al. Anti-Factor H autoantibodies associated with atypical hemolytic uremic syndrome. , 2005, Journal of the American Society of Nephrology : JASN.
[20] Benita J. O’Colmain,et al. Prevalence of age-related macular degeneration in the United States. , 2004, Archives of ophthalmology.
[21] A. Fletcher,et al. Age-related macular degeneration causing visual impairment in people 75 years or older in Britain: an add-on study to the Medical Research Council Trial of Assessment and Management of Older People in the Community. , 2004, Ophthalmology.
[22] G. Remuzzi,et al. Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease. , 2003, Human molecular genetics.
[23] J. Goodship,et al. Factor H mutations in hemolytic uremic syndrome cluster in exons 18-20, a domain important for host cell recognition. , 2001, American journal of human genetics.
[24] D. Pérez-Caballero,et al. Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome. , 2001, American journal of human genetics.
[25] G. Remuzzi,et al. The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20. , 2001, Journal of the American Society of Nephrology : JASN.
[26] R. Würzner. Modulation of complement membrane attack by local C7 synthesis , 2000, Clinical and experimental immunology.
[27] J. Goodship,et al. Genetic studies into inherited and sporadic hemolytic uremic syndrome. , 1998, Kidney international.
[28] P. Lachmann,et al. Molecular basis of the complement C7 M/N polymorphism. A neutral amino acid substitution outside the epitope of the allospecific monoclonal antibody WU 4-15. , 1995, Journal of immunology.
[29] R. Wurzner. The C7 M/N polymorphism is determined by a neutral amino acid substitution outside the epitope of the allospecific monoclonal antibody WU 4-15 , 1993 .
[30] R. Discipio. Formation and structure of the C5b-7 complex of the lytic pathway of complement. , 1992, The Journal of biological chemistry.
[31] P. Lachmann. Heberden oration 1986. Complement--friend or foe? , 1987, British journal of rheumatology.
[32] P. Lambert,et al. The complement system in hemolytic-uremic syndrome in childhood. , 1980, Clinical nephrology.
[33] K. Tokunaga,et al. A novel protein polymorphism of human complement C7 detected by a monoclonal antibody , 2004, Immunogenetics.
[34] Robert B Sim,et al. Sequence polymorphism of human complement factor H , 2004, Immunogenetics.
[35] M. Dierich,et al. Complement C7 M/N allotyping in infectious diseases. , 1995, Experimental and clinical immunogenetics.
[36] K. Tokunaga,et al. C7*N is a hypomorphic allele of the human complement c7 M/N protein polymorphism. , 1991, Experimental and clinical immunogenetics.
[37] O. Götze,et al. C7*9, a new frequent C7 allele detected by an allotype-specific monoclonal antibody. , 1990, Complement and inflammation.
[38] M. Pangburn,et al. Alternative pathway of complement. , 1988, Methods in enzymology.