Degradation of two novel congenital TTP ADAMTS13 mutants by the cell proteasome prevents ADAMTS13 secretion
Author:
Publisher
Elsevier BV
Subject
Hematology
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1. In vitro characterization of a novel Arg102 mutation in the ADAMTS13 metalloprotease domain;Journal of Thrombosis and Haemostasis;2023-03
2. Upshaw-Schulman syndrome-associated ADAMTS13 variants possess proteolytic activity at the surface of endothelial cells and in simulated circulation;PLOS ONE;2020-05-04
3. Two novel mutations in ADAMTS13 in a Chinese boy with congenital thrombocytopenic purpura: a case report;BMC Medical Genetics;2020-03-20
4. ADAMTS13: origins, applications, and prospects;Transfusion;2018-09-12
5. Child-onset thrombotic thrombocytopenic purpura caused by p.R498C and p.G259PfsX133 mutations in ADAMTS13;European Journal of Haematology;2018-06-25
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