Correction of ADAMTS13 Deficiency by In Utero Gene Transfer of Lentiviral Vector encoding ADAMTS13 Genes
Open Access
- 1 January 2009
- journal article
- Published by Elsevier in Molecular Therapy
- Vol. 17 (1) , 34-41
- https://doi.org/10.1038/mt.2008.223
Abstract
No abstract availableKeywords
This publication has 48 references indexed in Scilit:
- Factor VIII accelerates proteolytic cleavage of von Willebrand factor by ADAMTS13Proceedings of the National Academy of Sciences, 2008
- Platelet-VWF complexes are preferred substrates of ADAMTS13 under fluid shear stressBlood, 2008
- Efficient In Vivo Targeting of Epidermal Stem Cells by Early Gestational Intraamniotic Injection of Lentiviral Vector Driven by the Keratin 5 PromoterMolecular Therapy, 2008
- The cooperative activity between the carboxyl-terminal TSP1 repeats and the CUB domains of ADAMTS13 is crucial for recognition of von Willebrand factor under flowBlood, 2007
- Correction of junctional epidermolysis bullosa by transplantation of genetically modified epidermal stem cellsNature Medicine, 2006
- Apical sorting of ADAMTS13 in vascular endothelial cells and Madin-Darby canine kidney cells depends on the CUB domains and their association with lipid raftsBlood, 2006
- Increased ADAMTS‐13 proteolytic activity in rat hepatic stellate cells upon activation in vitro and in vivoJournal of Thrombosis and Haemostasis, 2006
- Factor VIII ectopically expressed in platelets: efficacy in hemophilia A treatmentBlood, 2003
- Modulation of Endothelial Cell Synthesis of von Willebrand Factor by Mononuclear Cell ProductsPathophysiology of Haemostasis and Thrombosis, 1988
- Unusually Large Plasma Factor VIII: von Willebrand Factor Multimers in Chronic Relapsing Thrombotic Thrombocytopenic PurpuraNew England Journal of Medicine, 1982