Inherited deficiencies of the terminal complement components.
about
Investigation for complement deficiency following meningococcal disease.Meningococcal meningitis in a patient with urticarial vasculitis: is there a link?The C5b-9 membrane attack complex of complement activation localizes to villous trophoblast injury in vivo and modulates human trophoblast function in vitro.Complement factor 5 (C5) p.A252T mutation is prevalent in, but not restricted to, sub-Saharan Africa: implications for the susceptibility to meningococcal disease.The cytolytically inactive terminal complement complex activates endothelial cells to express adhesion molecules and tissue factor procoagulant activity.
P2860
Inherited deficiencies of the terminal complement components.
description
1993 nî lūn-bûn
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1993年の論文
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1993年学术文章
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1993年学术文章
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1993年学术文章
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1993年学术文章
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1993年學術文章
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1993年學術文章
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1993年學術文章
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name
Inherited deficiencies of the terminal complement components.
@en
type
label
Inherited deficiencies of the terminal complement components.
@en
prefLabel
Inherited deficiencies of the terminal complement components.
@en
P2093
P2860
P1476
Inherited deficiencies of the terminal complement components.
@en
P2093
Nürnberger W
Perissutti S
P2860
P356
10.3109/08830189309051171
P577
1993-01-01T00:00:00Z