Early clinical data raise the bar for hemophilia gene therapies
Author:
Publisher
Springer Science and Business Media LLC
Subject
Biomedical Engineering,Molecular Medicine,Applied Microbiology and Biotechnology,Bioengineering,Biotechnology
Link
http://www.nature.com/articles/nbt1016-999.pdf
Reference5 articles.
1. Adenovirus-Associated Virus Vector–Mediated Gene Transfer in Hemophilia B
2. Long-Term Safety and Efficacy of Factor IX Gene Therapy in Hemophilia B
3. Biogen and UPenn join forces to commercialize gene therapies
4. First gene therapy approved
5. Factor VIII–Mimetic Function of Humanized Bispecific Antibody in Hemophilia A
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2. Immunogenicity of Recombinant Adeno-Associated Virus (AAV) Vectors for Gene Transfer;BioDrugs;2023-03-02
3. Protection is not always a good thing: The immune system’s impact on gene therapy;Genetics and Molecular Biology;2022
4. Exploring the Potential Feasibility of Intra-Articular Adeno-Associated Virus-Mediated Gene Therapy for Hemophilia Arthropathy;Human Gene Therapy;2020-04-01
5. Complexity of immune responses to AAV transgene products – Example of factor IX;Cellular Immunology;2019-08
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