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Pathogenicity of Anti-ADAMTS13 Autoantibodies in Acquired Thrombotic Thrombocytopenic Purpura.

EBioMedicine | 2015

Acquired thrombotic thrombocytopenic purpura (TTP) is an autoimmune disease in which anti-ADAMTS13 autoantibodies cause severe enzyme deficiency. ADAMTS13 deficiency causes the loss of regulation of von Willebrand factor multimeric size and platelet-tethering function, which results in the formation of disseminated microvascular platelet microthrombi. Precisely how anti-ADAMTS13 autoantibodies, or antibody subsets, cause ADAMTS13 deficiency (ADAMTS13 activity generally < 10%) has not been formally investigated.

Pubmed ID: 26425702 RIS Download

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Associated grants

  • Agency: British Heart Foundation, United Kingdom
    Id: FS/10/013/28073
  • Agency: Medical Research Council, United Kingdom
    Id: G0800671
  • Agency: British Heart Foundation, United Kingdom
    Id: PG/12/30/29498

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HEK293 (tool)

RRID:CVCL_0045

Cell line HEK293 is a Transformed cell line with a species of origin Homo sapiens (Human)

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