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Publications by Thierry VandenDriessche
Liver-Directed Lentiviral Gene Therapy in a Dog Model of Hemophilia B
Science Translational Medicine
Medicine
28. Intravenous Administration of Lentiviral Vectors Expressing Hyperactive Factor IX Converts Severe Into Mild Hemophilia B in a Canine Model
Molecular Therapy
Molecular Medicine
Molecular Biology
Pharmacology
Medicine
Genetics
Drug Discovery
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Immune Modulatory Cell Therapy for Hemophilia B Based on CD20-Targeted Lentiviral Gene Transfer to Primary B Cells
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447. Lentiviral Gene Therapy in a Preclinical Model of Omenn Syndrome
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Designer Nuclease-Mediated Gene Correction via Homology-Directed Repair in an in Vitro Model of Canine Hemophilia B
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Gene Therapy for Hemophilia
Frontiers in Bioscience - Landmark
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Generation of an Optimized Lentiviral Vector Encoding a High-Expression Factor VIII Transgene for Gene Therapy of Hemophilia A
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Hemophilia B Acquired Through Liver Transplantation
Liver Transplantation
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Lentiviral Gene Replacement Therapy of Retinas in a Mouse Model for Usher Syndrome Type 1B
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Platelet-Targeted Gene Therapy for Hemophilia
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