Correction of a Recessive Genetic Defect by CRISPR-Cas9-Mediated Endogenous Repair
Author:
Affiliation:
1. UOS-IRGB, Milan Unit, Italy and Humanitas Clinical and Research Center, Rozzano, Italy.
2. Biotechnology Research Center, Università Cattolica del Sacro Cuore, Cremona, Italy.
Publisher
Mary Ann Liebert Inc
Subject
Genetics,Biotechnology
Link
http://www.liebertpub.com/doi/pdf/10.1089/crispr.2018.0004
Reference42 articles.
1. A Programmable Dual-RNA–Guided DNA Endonuclease in Adaptive Bacterial Immunity
2. Multiplex Genome Engineering Using CRISPR/Cas Systems
3. RNA-Guided Human Genome Engineering via Cas9
4. The agents of natural genome editing
5. CRISPR/Cas9‐Directed Genome Editing of Cultured Cells
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1. CRISPR/Cas9-mediated gene knockout and interallelic gene conversion in human induced pluripotent stem cells using non-integrative bacteriophage-chimeric retrovirus-like particles;BMC Biology;2022-01-07
2. Pseudogene-Mediated Gene Conversion After CRISPR-Cas9 Editing Demonstrated by Partial CD33 Conversion with SIGLEC22P;The CRISPR Journal;2021-10-01
3. Pseudogene-mediated gene conversion after CRISPR-Cas9 editing demonstrated by partial CD33 conversion with SIGLEC22P;2021-04-20
4. Chromosome Transplantation: Correction of the Chronic Granulomatous Disease Defect in Mouse Induced Pluripotent Stem Cells;Stem Cells;2019-04-02
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