Adenovirus vectors in hematopoietic stem cell genome editing-Reference-Cited by-同舟云学术

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Adenovirus vectors in hematopoietic stem cell genome editing

Published:2019-11-20 Issue:24 Volume:593 Page:3623-3648
ISSN:0014-5793
Container-title:FEBS Letters
language:en
Short-container-title:FEBS Lett

Author:

Li Chang¹,Lieber André¹²

Affiliation:

1. Department of Medicine Division of Medical Genetics University of Washington Seattle WA USA

2. Department of Pathology University of Washington Seattle WA USA

Funder

National Heart, Lung, and Blood Institute

Publisher

Wiley

Subject

Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/1873-3468.13668

Reference255 articles.

1. The Use of DNA for Gene Therapy—the Need, Experimental Approach, and Implications

2. Gene Therapy for Human Genetic Disease?

3. Construction of a retrovirus packaging mutant and its use to produce helper-free defective retrovirus

4. Gene Therapy for Immunodeficiency Due to Adenosine Deaminase Deficiency

5. Gene Therapy of Human Severe Combined Immunodeficiency (SCID)-X1 Disease

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1. Auto-expansion of in vivo HDAd-transduced hematopoietic stem cells by constitutive expression of tHMGA2;Molecular Therapy - Methods & Clinical Development;2024-09

2. A simplified G-CSF–free procedure allows for in vivo HSC gene therapy of sickle cell disease in a mouse model;Blood Advances;2024-07-31

3. Exploring Advanced CRISPR Delivery Technologies for Therapeutic Genome Editing;Small Science;2024-07-25

4. Gutless Helper-Dependent and First-Generation HAdV5 Vectors Have Similar Mechanical Properties and Common Transduction Mechanisms;Human Gene Therapy;2024-03-01

5. Engineered stem cells by emerging biomedical stratagems;Science Bulletin;2024-01

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