A Cure For Hemophilia: the Promise Becomes a Reality
Author:
Publisher
Elsevier BV
Subject
Drug Discovery,Pharmacology,Genetics,Molecular Biology,Molecular Medicine
Reference1 articles.
1. Superior in vivo transduction of human hepatocytes using engineered AAV3 capsid;Vercauteren;Mol Ther,2016
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1. Immunogenicity of Recombinant Adeno-Associated Virus (AAV) Vectors for Gene Transfer;BioDrugs;2023-03-02
2. Exploring the Potential Feasibility of Intra-Articular Adeno-Associated Virus-Mediated Gene Therapy for Hemophilia Arthropathy;Human Gene Therapy;2020-04-01
3. Illness perceptions and their relation to physical activity in children and adolescents with hemophilia;Health Psychology and Behavioral Medicine;2020-01-01
4. Complexity of immune responses to AAV transgene products – Example of factor IX;Cellular Immunology;2019-08
5. Next Generation of Adeno-Associated Virus Vectors for Gene Therapy for Human Liver Diseases;Gastroenterology Clinics of North America;2019-06
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