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Article

Intravenous administration of an AAV-2 vector for the expression of factor IX in mice and a dog model of hemophilia B

1 Jan 2004

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Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 14712305
DOI: 10.1038/sj.gt.3302142

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Intravenous administration of an AAV-2 vector for the expression of factor IX in mice and a dog model of hemophilia BPMID 14712305Read ↗

Translational Data from Adeno-Associated Virus-Mediated Gene Therapy of Hemophilia B in DogsSemantic proximity Read ↗

Safety and efficacy of factor IX gene transfer to skeletal muscle in murine and canine hemophilia B models by adeno-associated viral vector serotype 1Semantic proximity Read ↗

AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia BSemantic proximity Read ↗

Evidence for gene transfer and expression of factor IX in haemophilia B patients treated with an AAV vectorSemantic proximity Read ↗

The efficacy and the risk of immunogenicity of FIX Padua (R338L) in hemophilia B dogs treated by AAV muscle gene therapy.Semantic proximity Read ↗

Gene therapy for hemophiliaSemantic proximity Read ↗

Protein Replacement Therapy and Gene Transfer in Canine Models of Hemophilia A, Hemophilia B, von Willebrand Disease, and Factor VII DeficiencySemantic proximity Read ↗

Total correction of hemophilia A mice with canine FVIII using an AAV 8 serotypeSemantic proximity Read ↗

Long-term correction of inhibitor-prone hemophilia B dogs treated with liver-directed AAV2-mediated factor IX gene therapySemantic proximity Read ↗

Gene therapy for hemophiliaSemantic proximity Read ↗

Adeno-Associated Virus Vectors and HematologySemantic proximity Read ↗

Adeno-associated viral vectors for the treatment of hemophiliaSemantic proximity Read ↗

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