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J P Atkinson

Showing results (231-240 of 235) with videos related to

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BJOG : an International Journal of Obstetrics and Gynaecology|February 4, 2021
Dysfunction of complement receptors CR3 (CD11b/18) and CR4 (CD11c/18) in pre-eclampsia: a genetic and functional studyA I Lokki, L Teirilä, M Triebwasser, et al.
Blood|April 21, 2001
Molecular identification of Knops blood group polymorphisms found in long homologous region D of complement receptor 1J M Moulds, P A Zimmerman, O K Doumbo, et al.
American Journal of Human Genetics|July 5, 2001
Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3R A Ophoff, J DeYoung, S K Service, 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.
Genes and Immunity|January 29, 2011
Evaluation of the TREX1 gene in a large multi-ancestral lupus cohortB Namjou, P H Kothari, J A Kelly, et al.
Pageof 24

Showing results (231-240 of 235) with videos related to

Sort By:
Pageof 24
You have reached the last page of results.This site can display upto 235 results.
BJOG : an International Journal of Obstetrics and Gynaecology|February 4, 2021
Dysfunction of complement receptors CR3 (CD11b/18) and CR4 (CD11c/18) in pre-eclampsia: a genetic and functional studyA I Lokki, L Teirilä, M Triebwasser, et al.
Blood|April 21, 2001
Molecular identification of Knops blood group polymorphisms found in long homologous region D of complement receptor 1J M Moulds, P A Zimmerman, O K Doumbo, et al.
American Journal of Human Genetics|July 5, 2001
Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3R A Ophoff, J DeYoung, S K Service, 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.
Genes and Immunity|January 29, 2011
Evaluation of the TREX1 gene in a large multi-ancestral lupus cohortB Namjou, P H Kothari, J A Kelly, et al.
Pageof 24