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135 related items for PubMed ID: 2468081
1. Effect of osmotic protection on nucleated cell killing by C5b-9: cell death is not affected by the prevention of cell swelling. Kim SH, Carney DF, Papadimitriou JC, Shin ML. Mol Immunol; 1989 Mar; 26(3):323-31. PubMed ID: 2468081 [Abstract] [Full Text] [Related]
2. Nucleated cell killing by complement: effects of C5b-9 channel size and extracellular Ca2+ on the lytic process. Kim SH, Carney DF, Hammer CH, Shin ML. J Immunol; 1987 Mar 01; 138(5):1530-6. PubMed ID: 2433349 [Abstract] [Full Text] [Related]
3. Complement lysis of U937, a nucleated mammalian cell line in the absence of C9: effect of C9 on C5b-8 mediated cell lysis. Morgan BP, Imagawa DK, Dankert JR, Ramm LE. J Immunol; 1986 May 01; 136(9):3402-6. PubMed ID: 3514758 [Abstract] [Full Text] [Related]
4. Elimination of terminal complement intermediates from the plasma membrane of nucleated cells: the rate of disappearance differs for cells carrying C5b-7 or C5b-8 or a mixture of C5b-8 with a limited number of C5b-9. Carney DF, Koski CL, Shin ML. J Immunol; 1985 Mar 01; 134(3):1804-9. PubMed ID: 3968432 [Abstract] [Full Text] [Related]
5. Bacterial killing by complement. C9-mediated killing in the absence of C5b-8. Dankert JR, Esser AF. Biochem J; 1987 Jun 01; 244(2):393-9. PubMed ID: 3311029 [Abstract] [Full Text] [Related]
6. Multimeric C9 within C5b-9 is required for inner membrane damage to Escherichia coli J5 during complement killing. Bloch EF, Schmetz MA, Foulds J, Hammer CH, Frank MM, Joiner KA. J Immunol; 1987 Feb 01; 138(3):842-8. PubMed ID: 3100618 [Abstract] [Full Text] [Related]
7. Elimination of terminal complement complexes in the plasma membrane of nucleated cells: influence of extracellular Ca2+ and association with cellular Ca2+. Carney DF, Hammer CH, Shin ML. J Immunol; 1986 Jul 01; 137(1):263-70. PubMed ID: 3711667 [Abstract] [Full Text] [Related]
8. Studies on the mechanism of bacterial resistance to complement-mediated killing. VI. IgG increases the bactericidal efficiency of C5b-9 for E. coli 0111B4 by acting at a step before C5 cleavage. Joiner KA, Goldman RC, Hammer CH, Leive L, Frank MM. J Immunol; 1983 Nov 01; 131(5):2570-5. PubMed ID: 6355297 [Abstract] [Full Text] [Related]
9. Membrane factors responsible for homologous species restriction of complement-mediated lysis: evidence for a factor other than DAF operating at the stage of C8 and C9. Shin ML, Hänsch G, Hu VW, Nicholson-Weller A. J Immunol; 1986 Mar 01; 136(5):1777-82. PubMed ID: 2419414 [Abstract] [Full Text] [Related]
10. The membrane attack complex of complement: C5b-8 complex as accelerator of C9 polymerization. Tschopp J, Podack ER, Müller-Eberhard HJ. J Immunol; 1985 Jan 01; 134(1):495-9. PubMed ID: 3964819 [Abstract] [Full Text] [Related]
11. Increased ion permeability of planar lipid bilayer membranes after treatment with the C5b-9 cytolytic attack mechanism of complement. Michaels DW, Abramovitz AS, Hammer CH, Mayer MM. Proc Natl Acad Sci U S A; 1976 Aug 01; 73(8):2852-6. PubMed ID: 1066698 [Abstract] [Full Text] [Related]
12. Increased susceptibility to erythrocyte C5b-9 deposition and complement-mediated lysis in chronic renal failure. Himmelfarb J, McMonagle E, Holbrook D, Hakim R. Kidney Int; 1999 Feb 01; 55(2):659-66. PubMed ID: 9987090 [Abstract] [Full Text] [Related]
13. Homologous species restriction in lysis of erythrocytes by terminal complement proteins. Hänsch GM, Hammer CH, Vanguri P, Shin ML. Proc Natl Acad Sci U S A; 1981 Aug 01; 78(8):5118-21. PubMed ID: 6946459 [Abstract] [Full Text] [Related]
14. C5b-9 assembly: average binding of one C9 molecule to C5b-8 without poly-C9 formation generates a stable transmembrane pore. Bhakdi S, Tranum-Jensen J. J Immunol; 1986 Apr 15; 136(8):2999-3005. PubMed ID: 3958488 [Abstract] [Full Text] [Related]
15. Inhibition of the lytic action of cell-bound terminal complement components by human high density lipoproteins and apoproteins. Rosenfeld SI, Packman CH, Leddy JP. J Clin Invest; 1983 Apr 15; 71(4):795-808. PubMed ID: 6403580 [Abstract] [Full Text] [Related]
16. Measurement of the ratio of the eighth and ninth components of human complement on complement-lysed membranes. Stewart JL, Monahan JB, Brickner A, Sodetz JM. Biochemistry; 1984 Aug 28; 23(18):4016-22. PubMed ID: 6487588 [Abstract] [Full Text] [Related]
17. Complement pores in erythrocyte membranes. Analysis of C8/C9 binding required for functional membrane damage. Sims PJ. Biochim Biophys Acta; 1983 Aug 10; 732(3):541-52. PubMed ID: 6871214 [Abstract] [Full Text] [Related]
18. Quantitative analysis of adenine nucleotides during the prelytic phase of cell death mediated by C5b-9. Papadimitriou JC, Ramm LE, Drachenberg CB, Trump BF, Shin ML. J Immunol; 1991 Jul 01; 147(1):212-7. PubMed ID: 1904901 [Abstract] [Full Text] [Related]
19. Multimeric complement component C9 is necessary for killing of Escherichia coli J5 by terminal attack complex C5b-9. Joiner KA, Schmetz MA, Sanders ME, Murray TG, Hammer CH, Dourmashkin R, Frank MM. Proc Natl Acad Sci U S A; 1985 Jul 01; 82(14):4808-12. PubMed ID: 3895225 [Abstract] [Full Text] [Related]
20. Human protectin (CD59), an 18,000-20,000 MW complement lysis restricting factor, inhibits C5b-8 catalysed insertion of C9 into lipid bilayers. Meri S, Morgan BP, Davies A, Daniels RH, Olavesen MG, Waldmann H, Lachmann PJ. Immunology; 1990 Sep 01; 71(1):1-9. PubMed ID: 1698710 [Abstract] [Full Text] [Related] Page: [Next] [New Search]