The Mesenchymal Stem Cells Derived from Transgenic Mice Carrying Human Coagulation Factor VIII Can Correct Phenotype in Hemophilia A Mice
Author:
Publisher
Elsevier BV
Subject
Genetics,Molecular Biology
Reference53 articles.
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2. Toward gene therapy for hemophilia A with novel adenoviral vectors: successes and limitations in canine models;Arruda;J. Thromb. Haemost.,2006
3. Confocal microscopy analysis of native, full length and B-domain deleted coagulation factor VIII trafficking in mammalian cells;Becker;Thromb. Haemost.,2004
4. Factors influencing therapeutic efficacy and the host immune response to helper-dependent adenoviral gene therapy in hemophilia A mice;Brown;J. Thromb. Haemost.,2004
5. Long-term persistence of human bone marrow stromal cells transduced with factor VIII-retroviral vectors and transient production of therapeutic levels of human factor VIII in nonmyeloablated immunodeficient mice;Chuah;Hum. Gene Ther.,2000
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