Highly Efficient CRISPR/Cas9‐Mediated Genome Editing in Human Pluripotent Stem Cells-Reference-Cited by-同舟云学术

Highly Efficient CRISPR/Cas9‐Mediated Genome Editing in Human Pluripotent Stem Cells

Published:2022-11 Issue:11 Volume:2 Page:
ISSN:2691-1299
Container-title:Current Protocols
language:en
Short-container-title:Current Protocols

Author:

Maguire Jean Ann¹,Gadue Paul¹²³,French Deborah L.¹²³

Affiliation:

1. Center for Cellular and Molecular Therapeutics The Children's Hospital of Philadelphia Philadelphia Pennsylvania

2. Department of Pathology and Laboratory Medicine The Children's Hospital of Philadelphia Philadelphia Pennsylvania

3. Department of Pathology and Laboratory Medicine University of Pennsylvania Philadelphia Pennsylvania

Funder

National Heart, Lung, and Blood Institute

National Institutes of Health

Publisher

Wiley

Subject

Medical Laboratory Technology,Health Informatics,General Pharmacology, Toxicology and Pharmaceutics,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cpz1.590

Reference16 articles.

1. Modeling rare diseases with induced pluripotent stem cell technology

2. Digestion of DNA with Restriction Endonucleases

3. May I Cut in? Gene Editing Approaches in Human Induced Pluripotent Stem Cells

4. Inhibition of 53BP1 favors homology-dependent DNA repair and increases CRISPR–Cas9 genome-editing efficiency

5. Evaluation of Homology-Independent CRISPR-Cas9 Off-Target Assessment Methods

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