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Journal of Thrombosis and Haemostasis : JTH|June 22, 2024
Venous thromboembolic disease genetics: from variants to functionMary Underwood, Christopher Bidlack, Karl C DeschCurrent Opinion in Hematology|August 7, 2015
Dissecting the genetic determinants of hemostasis and thrombosisKarl C DeschArteriosclerosis, Thrombosis, and Vascular Biology|May 26, 2007
Thrombotic thrombocytopenic purpura in humans and miceKarl C Desch, David G MottoBlood|May 28, 2020
Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic diseaseKarl C Desch, Ayse B Ozel, Matt Halvorsen, et al.Plos One|April 8, 2015
Probing ADAMTS13 substrate specificity using phage displayKarl C Desch, Colin Kretz, Andrew Yee, et al.Thrombosis Research|September 26, 2016
Degradation of two novel congenital TTP ADAMTS13 mutants by the cell proteasome prevents ADAMTS13 secretionMary Underwood, Flora Peyvandi, Isabella Garagiola, et al.Kidney International|November 25, 2018
α-galactosidase A deficiency promotes von Willebrand factor secretion in models of Fabry diseaseJustin J Kang, Nayiri M Kaissarian, Karl C Desch, et al.Proceedings of the National Academy of Sciences of the United States of America|July 15, 2015
Massively parallel enzyme kinetics reveals the substrate recognition landscape of the metalloprotease ADAMTS13Colin A Kretz, Manhong Dai, Onuralp Soylemez, et al.Pediatric Blood & Cancer|October 12, 2013
Congenital thrombotic thrombocytopenic purpura with novel mutations in three unrelated Turkish childrenAyse Metin, Sule Unal, Fatma Gümrük, et al.Pageof 4