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The Journal of Experimental Medicine|October 1, 1985
Decay-accelerating factor is present on paroxysmal nocturnal hemoglobinuria erythroid progenitors and lost during erythropoiesis in vitroJ G Moore, M M Frank, H J Müller-Eberhard, et al.The Journal of Clinical Investigation|February 1, 1974
Hereditary deficiency of the sixth component of complement in man. I. Immunochemical, biologic, and family studiesJ P Leddy, M M Frank, T Gaither, et al.Inflammation|December 1, 1984
Deficiency in C3b receptors on neutrophils of patients with chronic granulomatous disease and hyperimmunoglobulin-E recurrent infection (Job's) syndromeT A Gaither, J I Gallin, K Iida, et al.Journal of Immunology (Baltimore, Md. : 1950)|May 15, 1987
A complement-resistant HeLa cell line (T638) is blocked at the step of C3 depositionP Santi, K A Joiner, C H Hammer, et al.Blood|July 1, 1989
High-dose intravenous immunoglobulin modifies complement-mediated in vivo clearanceM Basta, P F Langlois, M Marques, et al.Inflammation|June 1, 1981
Binding of immunoglobulin- and complement-coated erythrocytes to human neutrophil subpopulationsS C Whited, M Santaella, M M Frank, et al.The Journal of Experimental Medicine|February 1, 1987
Deficiency of the homologous restriction factor in paroxysmal nocturnal hemoglobinuriaL S Zalman, L M Wood, M M Frank, et al.Journal of Immunology (Baltimore, Md. : 1950)|September 8, 1999
IgG and complement-mediated tissue damage in the absence of C2: evidence of a functionally active C2-bypass pathway in a guinea pig modelE Wagner, J L Platt, D N Howell, et al.The Journal of Clinical Investigation|January 1, 1989
Studies on phagocytosis in patients with acute bacterial infectionsH H Simms, M M Frank, T C Quinn, et al.Journal of Immunology (Baltimore, Md. : 1950)|November 21, 2001
Surfactant protein A regulates complement activationW T Watford, J R Wright, C G Hester, et al.Pageof 22