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Showing 1 to 2 of 2 for “"ADAMTS-13"”.

  1. Interaction Between the Metalloprotease ADAMTS-13 and the Proteins of the Alternative Pathway of the Complement System

    … who can not cleave VWF multimers due to genetic ADAMTS13 deficiency, we investigated the mechanism through which VWF modulates complement, and its pathophysiological implications for human diseases. Using assays of ex-vivo serum-induced C3 and C5b-9 deposits on endothelial cells we documented …

    the-open-u Repository record for Interaction Between the Metalloprotease ADAMTS-13 and the Proteins of the Alternative Pathway of the Complement System (opens in a new tab)

  2. Plasma ADAMTS13 activity in dogs with severe thrombocytopenia and presumed immune thrombocytopenia

    Background: In humans, deficiency of plasma ADAMTS-13, a von Willebrand factor cleaving enzyme, is an important cause of thrombocytopenia in immune thrombotic thrombocytopenic purpura (iTTP). This disease can be difficult to differentiate from immune thrombocytopenia (ITP) in people. Further …

    vt Repository record for Plasma ADAMTS13 activity in dogs with severe thrombocytopenia and presumed immune thrombocytopenia (opens in a new tab)