Inactivation of ADAMTS13 by plasmin as a potential cause of thrombotic thrombocytopenic purpura

Journal of Thrombosis and Haemostasis

Volumn 8, Issue 9, 2010, Pages 2053-2062

  Feys, H B ^a   Vandeputte, N ^a   Palla, R ^b   Peyvandi, F ^b   Peerlinck, K ^c   Deckmyn, H ^a   Lijnen, H R ^c   Vanhoorelbeke, K ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

^b UNIVERSITY OF MILAN   (Italy)

^c UNIVERSITY OF LEUVEN   (Belgium)

Author keywords

ADAMTS13; Plasmin; TTP

Indexed keywords

ALPHA 2 ANTIPLASMIN; AUTOANTIBODY; PLASMINOGEN; PLASMINOGEN ACTIVATOR; RECOMBINANT ENZYME; SERINE PROTEINASE; UROKINASE; VON WILLEBRAND FACTOR CLEAVING PROTEINASE;

ARTICLE; CASE REPORT; ENZYME ACTIVITY; ENZYME DEFICIENCY; ENZYME DEGRADATION; ENZYME INACTIVATION; GENE MUTATION; HUMAN; MALE; PRIORITY JOURNAL; PROTEIN DEGRADATION; REMISSION; THROMBOTIC THROMBOCYTOPENIC PURPURA; WESTERN BLOTTING;

ADAM PROTEINS; ADULT; ALPHA-2-ANTIPLASMIN; AUTOANTIBODIES; AUTOIMMUNITY; BLOTTING, WESTERN; FIBRINOLYSIN; HUMANS; MALE; MUTATION; PROTEIN STRUCTURE, TERTIARY; PURPURA, THROMBOTIC THROMBOCYTOPENIC; REMISSION INDUCTION;

EID: 77956486046     PISSN: 15387933     EISSN: 15387836     Source Type: Journal    
DOI: 10.1111/j.1538-7836.2010.03942.x     Document Type: Article

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