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B P Morgan

Showing results (241-250 of 247) with videos related to

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Journal of Immunology (Baltimore, Md. : 1950)|October 15, 1996
Molecular bases of combined subtotal deficiencies of C6 and C7: their effects in combination with other C6 and C7 deficienciesB A Fernie, R Würzner, A Orren, et al.
Molecular Immunology|March 23, 2010
Impact of compound heterozygous complement factor H mutations on development of atypical hemolytic uremic syndrome-A pedigree revisitedS A Johnson, J M Williams, S Hakobyan, et al.
Annals of Neurology|February 16, 1999
Miller Fisher anti-GQ1b antibodies: alpha-latrotoxin-like effects on motor end platesJ J Plomp, P C Molenaar, G M O'Hanlon, et al.
The Journal of Experimental Medicine|May 17, 2000
Innate recognition of bacteria in human milk is mediated by a milk-derived highly expressed pattern recognition receptor, soluble CD14M O Labéta, K Vidal, J E Nores, et al.
Journal of Thrombosis and Haemostasis : JTH|September 5, 2015
Thrombin-activatable fibrinolysis inhibitor influences disease severity in humans and mice with pneumococcal meningitisB B Mook-Kanamori, M Valls Serón, M Geldhoff, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 22, 2004
Complement regulation at the molecular level: the structure of decay-accelerating factorP Lukacik, P Roversi, J White, et al.
Human Molecular Genetics|March 30, 2021
The rare C9 P167S risk variant for age-related macular degeneration increases polymerization of the terminal component of the complement cascadeO McMahon, T M Hallam, S Patel, et al.
Pageof 25

Showing results (241-250 of 247) with videos related to

Sort By:
Pageof 25
You have reached the last page of results.This site can display upto 247 results.
Journal of Immunology (Baltimore, Md. : 1950)|October 15, 1996
Molecular bases of combined subtotal deficiencies of C6 and C7: their effects in combination with other C6 and C7 deficienciesB A Fernie, R Würzner, A Orren, et al.
Molecular Immunology|March 23, 2010
Impact of compound heterozygous complement factor H mutations on development of atypical hemolytic uremic syndrome-A pedigree revisitedS A Johnson, J M Williams, S Hakobyan, et al.
Annals of Neurology|February 16, 1999
Miller Fisher anti-GQ1b antibodies: alpha-latrotoxin-like effects on motor end platesJ J Plomp, P C Molenaar, G M O'Hanlon, et al.
The Journal of Experimental Medicine|May 17, 2000
Innate recognition of bacteria in human milk is mediated by a milk-derived highly expressed pattern recognition receptor, soluble CD14M O Labéta, K Vidal, J E Nores, et al.
Journal of Thrombosis and Haemostasis : JTH|September 5, 2015
Thrombin-activatable fibrinolysis inhibitor influences disease severity in humans and mice with pneumococcal meningitisB B Mook-Kanamori, M Valls Serón, M Geldhoff, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 22, 2004
Complement regulation at the molecular level: the structure of decay-accelerating factorP Lukacik, P Roversi, J White, et al.
Human Molecular Genetics|March 30, 2021
The rare C9 P167S risk variant for age-related macular degeneration increases polymerization of the terminal component of the complement cascadeO McMahon, T M Hallam, S Patel, et al.
Pageof 25