Essentials von Willebrand disease (VWD) is the most common inherited bleeding disorder. Gene therapy for VWD offers long-term therapy for VWD patients. Transposons efficiently integrate the large von Willebrand factor (VWF) cDNA in mice. Liver-directed transposons support sustained VWF expression with suboptimal multimerization.status: publishe
Up until recently, von Willebrand Factor (VWF) structure-function relationships have only been studi...
Circulating plasma levels of the coagulation protein von Willebrand factor (VWF) are highly variable...
Von Willebrand disease (VWD) is the most frequent inherited bleeding disorder and is due to quantita...
BACKGROUND: Type 3 von Willebrand disease (VWD) is characterized by complete absence of von Willebra...
Objective—Gene therapy for severe von Willebrand disease (vWD) seems an interesting treatment altern...
Objective-Gene therapy for severe von Willebrand disease (vWD) seems an interesting treatment altern...
Von Willebrand disease (VWD) is an inherited bleeding disorder, caused by quantitative (type 1 and 3...
Essentials Treatment options for von Willebrand disease (VWD) patients are limited. The p.P1127_C194...
Von Willebrand disease (VWD) is the most common inherited bleeding disorder. Patients mainly develop...
Von Willebrand factor (VWF) is a plasma glycoprotein that acts as a carrier for factor VIII in the c...
von Willebrand factor (VWF) is an abundant plasma glycoprotein that is essential for the maintenance...
von Willebrand factor (VWF) is a large multimeric adhesive glycoprotein with complex roles in thromb...
International audienceBackground: Treatment options for patients suffering from von Willebrand disea...
von Willebrand disease (VWD) is a bleeding disorder caused by quantitative (type 1 and 3) or qualita...
International audiencevon Willebrand disease (VWD) is characterized by its heterogeneous clinical ma...
Up until recently, von Willebrand Factor (VWF) structure-function relationships have only been studi...
Circulating plasma levels of the coagulation protein von Willebrand factor (VWF) are highly variable...
Von Willebrand disease (VWD) is the most frequent inherited bleeding disorder and is due to quantita...
BACKGROUND: Type 3 von Willebrand disease (VWD) is characterized by complete absence of von Willebra...
Objective—Gene therapy for severe von Willebrand disease (vWD) seems an interesting treatment altern...
Objective-Gene therapy for severe von Willebrand disease (vWD) seems an interesting treatment altern...
Von Willebrand disease (VWD) is an inherited bleeding disorder, caused by quantitative (type 1 and 3...
Essentials Treatment options for von Willebrand disease (VWD) patients are limited. The p.P1127_C194...
Von Willebrand disease (VWD) is the most common inherited bleeding disorder. Patients mainly develop...
Von Willebrand factor (VWF) is a plasma glycoprotein that acts as a carrier for factor VIII in the c...
von Willebrand factor (VWF) is an abundant plasma glycoprotein that is essential for the maintenance...
von Willebrand factor (VWF) is a large multimeric adhesive glycoprotein with complex roles in thromb...
International audienceBackground: Treatment options for patients suffering from von Willebrand disea...
von Willebrand disease (VWD) is a bleeding disorder caused by quantitative (type 1 and 3) or qualita...
International audiencevon Willebrand disease (VWD) is characterized by its heterogeneous clinical ma...
Up until recently, von Willebrand Factor (VWF) structure-function relationships have only been studi...
Circulating plasma levels of the coagulation protein von Willebrand factor (VWF) are highly variable...
Von Willebrand disease (VWD) is the most frequent inherited bleeding disorder and is due to quantita...