Developing Immunologically Inert Adeno-Associated Virus (AAV) Vectors for Gene Therapy: Possibilities and Limitations-Reference-Cited by-同舟云学术

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Developing Immunologically Inert Adeno-Associated Virus (AAV) Vectors for Gene Therapy: Possibilities and Limitations

Published:2014-05-12 Issue:12 Volume:14 Page:1072-1082
ISSN:1389-2010
Container-title:Current Pharmaceutical Biotechnology
language:en
Short-container-title:CPB

Author:

Selot Ruchita,Hareendran Sangeetha,Jayandharan Giridhara

Publisher

Bentham Science Publishers Ltd.

Subject

Pharmaceutical Science,Biotechnology

Cited by 27 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. Recent developments in gene therapy research in India;Journal of Biosciences;2024-02-20

2. Biodistribution of Therapeutic Small Interfering RNAs Delivered with Lipid-Substituted Polyethylenimine-Based Delivery Systems;Molecular Pharmaceutics;2024-01-31

3. miR-142: A Master Regulator in Hematological Malignancies and Therapeutic Opportunities;Cells;2023-12-30

4. Lipid nanoparticle-targeted mRNA formulation as a treatment for ornithine-transcarbamylase deficiency model mice;Molecular Therapy - Nucleic Acids;2023-09

5. Adeno-Associated Virus (AAV) - Based Gene Therapies for Retinal Diseases: Where are We?;The Application of Clinical Genetics;2023-05

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