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A mutation in the kringle domain of human factor XII that causes autoinflammation, disturbs zymogen quiescence, and accelerates activation.
Hofman ZLM, Clark CC, Sanrattana W, Nosairi A, Parr NMJ, Živkovic M, Krause K, Mahnke NA, Scheffel J, Hack CE, Maurer M, de Maat S, Maas C. Hofman ZLM, et al. Among authors: maas c. J Biol Chem. 2020 Jan 10;295(2):363-374. doi: 10.1074/jbc.RA119.009788. Epub 2019 Nov 26. J Biol Chem. 2020. PMID: 31771982 Free PMC article.
Contact system activation on endothelial cells.
de Maat S, de Groot PG, Maas C. de Maat S, et al. Among authors: maas c. Semin Thromb Hemost. 2014 Nov;40(8):887-94. doi: 10.1055/s-0034-1395159. Epub 2014 Nov 11. Semin Thromb Hemost. 2014. PMID: 25389102 Review.
Response to letter regarding article, "plasmin cleavage of von willebrand factor as an emergency bypass for ADAMTS13 deficiency in thrombotic microangiopathy".
Tersteeg C, de Maat S, De Meyer SF, Smeets MW, Barendrecht AD, Roest M, Pasterkamp G, Fijnheer R, Vanhoorelbeke K, de Groot PG, Maas C. Tersteeg C, et al. Among authors: maas c. Circulation. 2015 Jan 13;131(2):e19-20. doi: 10.1161/CIRCULATIONAHA.114.012802. Circulation. 2015. PMID: 25583061 No abstract available.
Defective glycosylation of coagulation factor XII underlies hereditary angioedema type III.
Björkqvist J, de Maat S, Lewandrowski U, Di Gennaro A, Oschatz C, Schönig K, Nöthen MM, Drouet C, Braley H, Nolte MW, Sickmann A, Panousis C, Maas C, Renné T. Björkqvist J, et al. Among authors: maas c. J Clin Invest. 2015 Aug 3;125(8):3132-46. doi: 10.1172/JCI77139. Epub 2015 Jul 20. J Clin Invest. 2015. PMID: 26193639 Free PMC article.
Keeping von Willebrand Factor under Control: Alternatives for ADAMTS13.
Tersteeg C, Fijnheer R, Pasterkamp G, de Groot PG, Vanhoorelbeke K, de Maat S, Maas C. Tersteeg C, et al. Among authors: maas c. Semin Thromb Hemost. 2016 Feb;42(1):9-17. doi: 10.1055/s-0035-1564838. Epub 2015 Nov 23. Semin Thromb Hemost. 2016. PMID: 26595154 Review.
379 results