ADAMTS13 autoantibodies cloned from patients with acquired thrombotic thrombocytopenic purpura: 1. Structural and functional characterization in vitro
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Title
ADAMTS13 autoantibodies cloned from patients with acquired thrombotic thrombocytopenic purpura: 1. Structural and functional characterization in vitro
Authors
Keywords
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Journal
TRANSFUSION
Volume 56, Issue 7, Pages 1763-1774
Publisher
Wiley
Online
2016-04-04
DOI
10.1111/trf.13584
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- High-resolution epitope mapping by HX MS reveals the pathogenic mechanism and a possible therapy for autoimmune TTP syndrome
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- Allosteric activation of ADAMTS13 by von Willebrand factor
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- Conformational activation of ADAMTS13
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- Impact of new sequencing technologies on studies of the human B cell repertoire
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- Rituximab for thrombotic thrombocytopenic purpura: benefit of early administration during acute episodes and use of prophylaxis to prevent relapse
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- Residues Arg568 and Phe592 contribute to an antigenic surface for anti-ADAMTS13 antibodies in the spacer domain
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- Amino acid residues Arg659, Arg660, and Tyr661 in the spacer domain of ADAMTS13 are critical for cleavage of von Willebrand factor
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