RICE CRISPR: Rapidly increased cut ends by an exonuclease Cas9 fusion in zebrafish
Author:
Affiliation:
1. Department of BioSciences; Rice University; Houston Texas
2. Department of Neurosurgery; University of Texas M. D. Anderson Cancer Center; Houston Texas
Funder
National Institutes of Health
National Institute of Neurological Disorders and Stroke
Publisher
Wiley
Subject
Cell Biology,Endocrinology,Genetics
Reference19 articles.
1. CRISPR-STAT: An easy and reliable PCR-based method to evaluate target-specific sgRNA activity;Carrington;Nucleic Acids Research,2015
2. Dynamic imaging of genomic loci in living human cells by an optimized CRISPR/Cas system;Chen;Cell,2013
3. Long non-coding RNAs: New players in cell differentiation and development;Fatica;Nature Reviews Genetics,2014
4. Efficient mutagenesis by Cas9 protein-mediated oligonucleotide insertion and large-scale assessment of single-guide RNAs;Gagnon;PLoS ONE,2014
5. Evaluation of off-target and on-target scoring algorithms and integration into the guide RNA selection tool CRISPOR;Haeussler;Genome Biology,2016
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3. Genetic mechanisms of multiciliated cell development: from fate choice to differentiation in zebrafish and other models;The FEBS Journal;2023-12
4. TREX2 enables efficient genome disruption mediated by paired CRISPR-Cas9 nickases that generate 3′-overhanging ends;Molecular Therapy - Nucleic Acids;2023-12
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