Gene therapy for haemophilia
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2001.03225.x/fullpdf
Reference115 articles.
1. Human gene therapy;Anderson;Nature,1998
2. Expression of human factor IX in rabbit hepatocytes by retrovirus mediated gene transfer: potential for gene therapy of hemophilia B;Armentano;Proceedings of the National Academy of Science of the USA,1990
3. Phenotypic correction of factor IX deficiency in skin fibroblasts of hemophilic dogs;Axelrod;Proceedings of the National Academy of Science of the USA,1990
4. Sustained high-level expression of full-length human factor VIII and restoration of clotting activity in hemophilic mice using a minimal adenovirus vector;Balague;Blood,2000
5. Second generation, B-domain deleted recombinant factor VIII;Berntorp;Thrombosis and Haemostasis,1997
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1. Minimizing the Inhibitory Effect of Neutralizing Antibody for Efficient Gene Expression in the Liver With Adeno-associated Virus 8 Vectors;Molecular Therapy;2013-02
2. Disorders of Hemostasis;Rosen's Emergency Medicine – Concepts and Clinical Practice;2010
3. Liver-restricted expression of the canine factor VIII gene facilitates prevention of inhibitor formation in factor VIII-deficient mice;The Journal of Gene Medicine;2009-11
4. Protein Replacement Therapy and Gene Transfer in Canine Models of Hemophilia A, Hemophilia B, von Willebrand Disease, and Factor VII Deficiency;ILAR Journal;2009-01-01
5. Preclinical experiment of auxiliary partial orthotopic liver transplantation as a curative treatment for hemophilia;Liver Transplantation;2005
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