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- W1567100692 abstract "Historically, aPL antibodies were classified based on the clinical laboratory test in which they were detected, i.e. LA and aCL antibodies. It is now widely accepted that aPL antibodies are a heterogenous group of antibodies that react with a myriad of phospholipids (PLs), PL-protein complexes and PL binding proteins. The main antigenic target of these antibodies is recognized to be 2glycoprotein I (2GPI), which along with prothrombin accounts for more than 90% of the antibody binding activity in APS patients. Other potentially significant antigenic targets include tissue plasminogen activator (tPA), phosphatidylserine (PS), plasmin, annexin 2, activated protein C (APC), thrombin, antithrombin (AT) and annexin A5 [2,3]." @default.
- W1567100692 created "2016-06-24" @default.
- W1567100692 creator A5040395107 @default.
- W1567100692 creator A5061036069 @default.
- W1567100692 creator A5065463612 @default.
- W1567100692 creator A5079058927 @default.
- W1567100692 date "2012-04-20" @default.
- W1567100692 modified "2023-09-26" @default.
- W1567100692 title "Antiphospholipid Syndrome - An Evolving Story of a Multisystemic Disease" @default.
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