Bound Protein- and Peptide-Based Strategies for Adeno-Associated Virus Vector-Mediated Gene Therapy: Where Do We Stand Now?-Reference-Cited by-同舟云学术

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Bound Protein- and Peptide-Based Strategies for Adeno-Associated Virus Vector-Mediated Gene Therapy: Where Do We Stand Now?

Published:2020-11-01 Issue:21-22 Volume:31 Page:1146-1154
ISSN:1043-0342
Container-title:Human Gene Therapy
language:en
Short-container-title:Human Gene Therapy

Author:

Zhang Xintao¹,Chai Zheng¹,Samulski R. Jude¹²,Li Chengwen¹³⁴

Affiliation:

1. Gene Therapy Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA; Departments of

2. Pharmacology and

3. Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA

4. Carolina Institute for Developmental Disabilities, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

Publisher

Mary Ann Liebert Inc

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

https://www.liebertpub.com/doi/pdf/10.1089/hum.2020.193

Reference73 articles.

1. Engineering adeno-associated virus vectors for gene therapy

2. Gene therapy comes of age

3. Phase 1 Gene Therapy for Duchenne Muscular Dystrophy Using a Translational Optimized AAV Vector

4. Successful transduction of liver in hemophilia by AAV-Factor IX and limitations imposed by the host immune response

5. Adenovirus-Associated Virus Vector–Mediated Gene Transfer in Hemophilia B

Cited by 6 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. Therapeutic Application and Structural Features of Adeno-Associated Virus Vector;Current Issues in Molecular Biology;2024-08-02

2. The use of melittin to enhance transgene expression mediated by recombinant adeno-associated virus serotype 2 vectors both in vitro and in vivo;Journal of Integrative Medicine;2023-01

3. Customized blood-brain barrier shuttle peptide to increase AAV9 vector crossing the BBB and augment transduction in the brain;Biomaterials;2022-02

4. Preparation of Ultrasmall Gold Nanoparticles for Nuclear-Based Gene Delivery;Biomaterial Engineering;2022

5. Capsid-Engineering for Central Nervous System-Directed Gene Therapy with Adeno-Associated Virus Vectors;Human Gene Therapy;2021-10-01

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