Preclinical Gene Therapy Studies for Hemophilia Using Adeno-Associated Virus (AAV) Vectors
Author:
Publisher
Georg Thieme Verlag KG
Subject
Cardiology and Cardiovascular Medicine,Hematology
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-2004-825630
Cited by 23 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. MiR133b‐mediated inhibition of EGFR‐PTK pathway promotes rAAV2 transduction by facilitating intracellular trafficking and augmenting second‐strand synthesis;Journal of Cellular and Molecular Medicine;2023-07-19
2. Uncertainty in an era of transformative therapy for haemophilia: Addressing the unknowns;Haemophilia;2020-06-02
3. De novo formed satellite DNA-based mammalian artificial chromosomes and their possible applications;Chromosome Research;2015-01-18
4. The History of Hemophilia;Seminars in Thrombosis and Hemostasis;2014-06-09
5. Mammalian Artificial Chromosomes and Clinical Applications for Genetic Modification of Stem Cells: An Overview;Methods in Molecular Biology;2011
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