Combining CRISPR-Cas-mediated terminal resolution with a novel genetic workflow to achieve high-diversity adenoviral libraries-Reference-Cited by-同舟云学术

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Combining CRISPR-Cas-mediated terminal resolution with a novel genetic workflow to achieve high-diversity adenoviral libraries

Published:2024-06 Issue:2 Volume:32 Page:101241
ISSN:2329-0501
Container-title:Molecular Therapy - Methods & Clinical Development
language:en
Short-container-title:Molecular Therapy - Methods & Clinical Development

Author:

Fischer Julian^ORCID,Fedotova Ariana,Jaki Lena,Sallard Erwan,Erhardt Anja,Fuchs Jonas,Ruzsics Zsolt^ORCID

Funder

Bundesministerium fur Bildung und Forschung Dienststelle Berlin

Deutsche Forschungsgemeinschaft

Publisher

Elsevier BV

Reference78 articles.

1. Viral vector-based gene therapies in the clinic;Zhao;Bioeng. Transl. Med.,2022

2. Adenovirus-mediated gene delivery: Potential applications for gene and cell-based therapies in the new era of personalized medicine;Lee;Genes Dis.,2017

3. Adenovirus Vectors for Gene Therapy, Vaccination and Cancer Gene Therapy;Wold;Curr. Gene Ther.,2013

4. Adenoviral vectors for cardiovascular gene therapy applications: a clinical and industry perspective;Jt;J. Mol. Med.,2022

5. Identification of a myotropic AAV by massively parallel in vivo evaluation of barcoded capsid variants;Weinmann;Nat. Commun.,2020

Cited by 2 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. Building sustainable libraries by embracing diversity and inclusion in Digital Era;Information System and Smart City;2024-07-25

2. Expanding the Scope of Adenoviral Vectors by Utilizing Novel Tools for Recombination and Vector Rescue;Viruses;2024-04-23

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