Complement C3 variant and the risk of age-related macular degeneration.
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I. Deary | D. Clayton | A. Bird | A. Wright | C. Hayward | A. Moore | T. Sepp | J. Yates | B. Dhillon | J. Khan | H. Shahid | A. Armbrecht | J. Morgan | D. Thurlby | Baljinder K. Matharu | E. Redmond | A. Wright | A. Moore | A. Wright | A. Wright | A. Wright | A. Wright
[1] Johanna M Seddon,et al. The genetics of age-related macular degeneration: a review of progress to date. , 2006, Survey of ophthalmology.
[2] P. Mathieson,et al. Molecular analysis of C3 allotypes in patients with nephritic factor , 1993, Clinical and experimental immunology.
[3] P T de Jong,et al. An international classification and grading system for age-related maculopathy and age-related macular degeneration , 1995 .
[4] N. Behrendt,et al. A novel polymorphism of human complement component C3 detected by means of a monoclonal antibody , 2004, Immunogenetics.
[5] P. Mathieson,et al. Molecular analysis of C3 allotypes in patients with systemic vasculitis. , 1994, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[6] N. Orr,et al. A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degeneration , 2006, Nature Genetics.
[7] D. Patel,et al. Ocular complications in acquired partial lipodystrophy , 2006, Postgraduate Medical Journal.
[8] T. Welch,et al. Functional consequences of the genetic polymorphism of the third component of complement. , 1990, The Journal of pediatrics.
[9] Gudmundur A. Thorisson,et al. The International HapMap Project Web site. , 2005, Genome research.
[10] D. Clayton,et al. Complement Factor H Variant Y 402 H Is a Major Risk Determinant for Geographic Atrophy and Choroidal Neovascularization in Smokers and Nonsmokers , 2006 .
[11] J. Winkelstein,et al. Genetically determined variation in the complement system: relationship to disease. , 1984, The Journal of pediatrics.
[12] Yun Li,et al. CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration , 2006, Nature Genetics.
[13] P.T.V.M. de Jong,et al. Mechanisms of disease: Age-related macular degeneration , 2006 .
[14] 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.
[15] A. Edwards,et al. Complement Factor H Polymorphism and Age-Related Macular Degeneration , 2005, Science.
[16] John D Lambris,et al. Membranoproliferative glomerulonephritis type II (dense deposit disease): an update. , 2005, Journal of the American Society of Nephrology : JASN.
[17] C. Barnstable,et al. HTRA1 Promoter Polymorphism in Wet Age-Related Macular Degeneration , 2006, Science.
[18] M. Rambausek,et al. Genetic polymorphism of C3 and Bf in IgA nephropathy. , 1987, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[19] Ian J Deary,et al. The impact of childhood intelligence on later life: following up the Scottish mental surveys of 1932 and 1947. , 2004, Journal of personality and social psychology.
[20] O. Smithies,et al. Genetic polymorphism of C'3(beta1C-globulin) in human serum. , 1968, Science.
[21] M. Walport. Complement. First of two parts. , 2001, The New England journal of medicine.
[22] D. Clayton,et al. Complement factor H variant Y402H is a major risk determinant for geographic atrophy and choroidal neovascularization in smokers and nonsmokers. , 2006, Investigative ophthalmology & visual science.
[23] H. Arvilommi. Capacity of complement C3 phenotypes to bind on to mononuclear cells in man , 1974, Nature.
[24] D. Weeks,et al. Susceptibility genes for age-related maculopathy on chromosome 10q26. , 2005, American journal of human genetics.
[25] N. Camp,et al. A Variant of the HTRA1 Gene Increases Susceptibility to Age-Related Macular Degeneration , 2006, Science.
[26] J. Gilbert,et al. Complement Factor H Variant Increases the Risk of Age-Related Macular Degeneration , 2005, Science.
[27] M. Walport,et al. Comparison of the binding of C3S and C3F to complement receptors types 1, 2, and 3. , 1995, Journal of immunology.
[28] M. Walport,et al. Molecular basis of polymorphisms of human complement component C3 , 1990, The Journal of experimental medicine.
[29] M. Walport,et al. Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H , 2002, Nature Genetics.
[30] H. Kaplan,et al. Immunotherapy for choroidal neovascularization in a laser-induced mouse model simulating exudative (wet) macular degeneration , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[31] Johanna M Seddon,et al. Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration , 2006, Nature Genetics.
[32] O. Smithies,et al. Genetic Polymorphism of C'3(β1c-Globuiin) in Human Serum , 1968, Science.
[33] S. Russell,et al. Drusen associated with aging and age‐related macular degeneration contain proteins common to extracellular deposits associated with atherosclerosis, elastosis, amyloidosis, and dense deposit disease , 2000, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[34] G. Hageman,et al. Structure and composition of drusen associated with glomerulonephritis: Implications for the role of complement activation in drusen biogenesis , 2001, Eye.
[35] R. T. Smith,et al. Variation in factor B (BF) and complement component 2 (C2) genes is associated with age-related macular degeneration , 2006, Nature Genetics.
[36] D. Colville,et al. Visual impairment caused by retinal abnormalities in mesangiocapillary (membranoproliferative) glomerulonephritis type II ("dense deposit disease"). , 2003, American journal of kidney diseases : the official journal of the National Kidney Foundation.
[37] J. H. Jansen,et al. Hereditary porcine membranoproliferative glomerulonephritis type II is caused by factor H deficiency. , 1995, The Journal of clinical investigation.
[38] C. Barnstable,et al. Supporting Online Material for HTRA 1 Promoter Polymorphism in Wet Age-Related Macular Degeneration , 2006 .
[39] R. Vaughan,et al. Influence of donor C3 allotype on late renal-transplantation outcome. , 2006, The New England journal of medicine.
[40] A. Goldman,et al. Structure of complement factor H carboxyl‐terminus reveals molecular basis of atypical haemolytic uremic syndrome , 2006, The EMBO journal.
[41] Piet Gros,et al. Structure of C3b reveals conformational changes that underlie complement activity , 2006, Nature.
[42] J L McRae,et al. 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) , 2005, Journal of Medical Genetics.