Haemophilia replacement factors, both plasma-derived and recombinant, are in relatively short supply and are high-cost products. This has stymied the study and development of alternative methods of administration of haemophilia therapy even in the most economically advanced countries, owing to the large amounts of material needed because bioabsorption and bioavailability of haemophilic factors can be less than 10% when using non-intravenous routes of delivery. There is therefore a need to increase access to therapy worldwide by decreasing the cost and increasing the abundance so that therapy can be achieved through simplified, alternative delivery methods. Transgenic livestock have been used to produce haemophilic factors in milk. Only the ...
(F.IX), resulting in a deficiency in the ability of blood to clot. In addition to increased propensi...
Hemophilia is a genetic disease caused by a deficiency of one of the coagulation proteins. The term ...
The development of inhibitors to replacement factor therapy is a serious complication in the treatme...
Haemophilia replacement factors, both plasma-derived and recombinant, are in relatively short supply...
Hemophilia B is the congenital bleeding disorder caused by deficiency in functional coagulation fact...
Hemophilia B is the congenital bleeding disorder caused by deficiency in functional coagulation fact...
A non-human transgenic mammalian animal, as described above, contains an exogenous double stranded D...
The X-linked bleeding disorder hemophilia is caused by mutations in coagulation factor VIII (hemophi...
Dogs with hemophilia A, hemophilia B, von Willebrand disease (VWD), and factor VII deficiency faithf...
Factor IX deficiency (hemophilia B) is less common than factor VIII deficiency (hemophilia A) and in...
Recombinant DNA technology has led to accelerating introduction of novel therapeutics for the treatm...
Recombinant Factor IX characterized by a high percentage of active protein can be obtained in the mi...
Background—Current manufacturing methods for recombinant human Factor VIII (rFVIII) within mammalian...
It is essential to improve therapies for controlling excessive bleeding in patients with haemorrhagi...
Steven PipeDepartment of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, MI...
(F.IX), resulting in a deficiency in the ability of blood to clot. In addition to increased propensi...
Hemophilia is a genetic disease caused by a deficiency of one of the coagulation proteins. The term ...
The development of inhibitors to replacement factor therapy is a serious complication in the treatme...
Haemophilia replacement factors, both plasma-derived and recombinant, are in relatively short supply...
Hemophilia B is the congenital bleeding disorder caused by deficiency in functional coagulation fact...
Hemophilia B is the congenital bleeding disorder caused by deficiency in functional coagulation fact...
A non-human transgenic mammalian animal, as described above, contains an exogenous double stranded D...
The X-linked bleeding disorder hemophilia is caused by mutations in coagulation factor VIII (hemophi...
Dogs with hemophilia A, hemophilia B, von Willebrand disease (VWD), and factor VII deficiency faithf...
Factor IX deficiency (hemophilia B) is less common than factor VIII deficiency (hemophilia A) and in...
Recombinant DNA technology has led to accelerating introduction of novel therapeutics for the treatm...
Recombinant Factor IX characterized by a high percentage of active protein can be obtained in the mi...
Background—Current manufacturing methods for recombinant human Factor VIII (rFVIII) within mammalian...
It is essential to improve therapies for controlling excessive bleeding in patients with haemorrhagi...
Steven PipeDepartment of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, MI...
(F.IX), resulting in a deficiency in the ability of blood to clot. In addition to increased propensi...
Hemophilia is a genetic disease caused by a deficiency of one of the coagulation proteins. The term ...
The development of inhibitors to replacement factor therapy is a serious complication in the treatme...