Alpha-1 Antitrypsin Deficiency as a Candidate for Gene Editing
Author:
Affiliation:
1. Editor-in-Chief
Publisher
Mary Ann Liebert Inc
Subject
Genetics,Molecular Biology,Molecular Medicine
Link
http://www.liebertpub.com/doi/pdf/10.1089/hum.2018.29070.trf
Reference4 articles.
1. The prevalence of alpha-1 antitrypsin deficiency in Ireland
2. Amelioration of Alpha-1 Antitrypsin Deficiency Diseases with Genome Editing in Transgenic Mice
3. In Vivo Genome Editing Partially Restores Alpha1-Antitrypsin in a Murine Model of AAT Deficiency
4. Survival Advantage of Both Human Hepatocyte Xenografts and Genome-Edited Hepatocytes for Treatment of α-1 Antitrypsin Deficiency
Cited by 3 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. Gene therapy for alpha-1 antitrypsin deficiency: an update;Expert Opinion on Biological Therapy;2023-03-02
2. Applications of innovative gene-editing technologies in respiratory diseases;The Lung;2021
3. New Directions in Pulmonary Gene Therapy;Human Gene Therapy;2020-09-01
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