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Studies of a hypo-morphic variant of human C3
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Partial lipodystrophy, C3 nephritic factor and clinically inapparent mesangiocapillary glomerulonephritis
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Bennett, W. M.; Bardana, E. J.; Wuepper, K.; Houghton, D.; Border, W. A.; Götze, O., and Schreiber, R.: Partial lipodystrophy, C3 nephritic factor and clinically inapparent mesangiocapillary glomerulonephritis. Am J. Med. 62: 757-760 (1977).
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0017090694
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Nephritic factor: Description of a new quantitative assay and findings in glomerulonephritis
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Border W.; Wilson, C. B., and Gotze, O.: Nephritic factor: description of a new quantitative assay and findings in glomerulonephritis. Kidney int. 10: 311-318(1976)
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Border, W.1
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Studies of C3 polymorphism. Re-lationship between phenotype and conversion rates in vitro
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Bronnestam, R.: Studies of C3 polymorphism. Re-lationship between phenotype and conversion rates in vitro. Hum. Hered. 23: 220-225 (1973).
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Metabolic studies of the third component of complement and the glycine-rich beta glycoprotein in patients with hypocomplementemia
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Charlesworth J. D.: Williams, D. G.; Shcrington, E.; Lachmann, P. I., and Peters, D. K.: Metabolic studies of the third component of complement and the glycine-rich beta glycoprotein in patients with hypocomplementemia. J. clin. Invest. 53: 1578-1587 (1974).
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6
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0017762516
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The incorporation of C3 nephritic factor (C3NeF) into a stabilized C3 convertase, C3hUb (C3NeF) and its release after decay of convertase function
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Daha M. R.: Austen, K. F., and Fearon D. T.: The incorporation of C3 nephritic factor (C3NeF) into a stabilized C3 convertase, C3hUb (C3NeF). and its release after decay of convertase function. J. Immun. 119: 812-817 (1977).
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Daha, M.R.1
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0017780751
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Transfer of C3 nephritic factor from mother to fetus. Is C3 nephritic factor IgG?
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Davis, A. E.: Arnaout M. A.: Alper C. A., and Rosen F. S.: Transfer of C3 nephritic factor from mother to fetus. Is C3 nephritic factor IgG? New Engl J. Med. 297: 144-145 (1977).
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Davis, A.E.1
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8
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0017177146
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Inherited deficiency of the second component of complement. Rheumatic disease associations
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Glass D.; Raum, D.: Gibson D.: Stillman J. S. and Shur P. H.: Inherited deficiency of the second component of complement. Rheumatic disease associations. J. clin. Invest. 58: 853-861 (1976).
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0016733991
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Dense deposit disease: A variant of membranoproliferative glomerulonephritis
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Habib R.; Gubler, M. C; Loirat, C; Maize, H. B., and Levy, M.: Dense deposit disease: a variant of membranoproliferative glomerulonephritis. Kidney int. 7: 204-215 (1975).
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Recurrence of membranoproliferative glomerulonephritis following kidney transplantation
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McLean R. H.; Geiger, H.; Burke B.: Simmons, R.; Najarian, J.: Vernier, R. L., and Michael, A. F.: Recurrence of membranoproliferative glomerulonephritis following kidney transplantation. Am J. Med. 60: 60-72 (1976).
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Hypomorphic variant of C3, arthritis and chronic glomerulonephritis
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McLean, R.; Weinstein A.: Damjanov, I., and Rothfield N.: Hypomorphic variant of C3, arthritis and chronic glomerulonephritis. J. Pediat. 93: 937-943 (1978).
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Immunity deficiency in pathogenesis of glomerulonephritis
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Peters, D. K. and Lachmann P. J.: Immunity deficiency in pathogenesis of glomerulonephritis. Lancet i: 58-60 (1974).
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The complement abnormalities of lipodystrophy
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Sissons J. G. P.; West R. J.; Fallows J.; Williams, D. G.; Boucher, B. J.: Amos N., and Peters, D. K.: The complement abnormalities of lipodystrophy. New Engl J. Med. 294: 461-465 (1975).
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High voltage agarose electrophoresis in the study of C3 polymorphism
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Teisberg P.: High voltage agarose electrophoresis in the study of C3 polymorphism. Vox Sang. 19: 47-56 (1970).
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Teisberg, P.1
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C3 inactivation factor in thescrum of a patient with chronic hypocomplementemic proliferative glomerulonephritis
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Thompson R. A.: C3 inactivation factor in thescrum of a patient with chronic hypocomplementemic proliferative glomerulonephritis. Immunology 22: 147-158 (1972).
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Thompson, R.A.1
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