Journal article
CRISPR Repair Reveals Causative Mutation in a Preclinical Model of Retinitis Pigmentosa: A Brief Methodology
Methods in molecular biology (Clifton, N.J.), Vol.1715, pp.191-205
2018
DOI: 10.1007/978-1-4939-7522-8_13
PMCID: PMC9119419
PMID: 29188514
Abstract
CRISPR/Cas9 genome engineering is currently the leading genome surgery technology in most genetics laboratories. Combined with other complementary techniques, it serves as a powerful tool for uncovering genotype-phenotype correlations. Here, we describe a simplified protocol that was used in our publication, CRISPR Repair Reveals Causative Mutation in a Preclinical Model of Retinitis Pigmentosa, providing an overview of each section of the experimental process.
Details
- Title: Subtitle
- CRISPR Repair Reveals Causative Mutation in a Preclinical Model of Retinitis Pigmentosa: A Brief Methodology
- Creators
- Wen-Hsuan Wu - Department of Ophthalmology, Columbia University, New York, NY, USAYi-Ting Tsai - Department of Ophthalmology, Columbia University, New York, NY, USASally Justus - Department of Ophthalmology, Columbia University, New York, NY, USAGalaxy Y Cho - Department of Ophthalmology, Columbia University, New York, NY, USAJesse D Sengillo - State University of New York Downstate Medical Center, Brooklyn, NY, USAYu Xu - Department of Ophthalmology, Xinhua Hospital affiliated to Shanghai Jiao Tong, University School of Medicine, Shanghai, ChinaThiago Cabral - Department of Ophthalmology, Federal University of Espírito Santo (UFES), Vitória, BrazilChyuan-Sheng Lin - Department of Pathology & Cell Biology, Columbia University Medical Center, New York, NY, USAAlexander G Bassuk - Department of Pediatrics and Neurology, University of Iowa, Iowa City, IA, USAVinit B Mahajan - Department of Ophthalmology, Byers Eye Institute, Stanford University , Palo Alto, CA, USAStephen H Tsang - Edward S. Harkness Eye Institute, Columbia University, New York, NY, USA. sht2@cumc.columbia.edu
- Resource Type
- Journal article
- Publication Details
- Methods in molecular biology (Clifton, N.J.), Vol.1715, pp.191-205
- DOI
- 10.1007/978-1-4939-7522-8_13
- PMID
- 29188514
- PMCID
- PMC9119419
- NLM abbreviation
- Methods Mol Biol
- eISBN
- 9781493975228; 1493975226
- ISSN
- 1064-3745
- eISSN
- 1940-6029
- Publisher
- United States
- Grant note
- R01 EY025225 / NEI NIH HHS R01 EY018213 / NEI NIH HHS R01 NS098590 / NINDS NIH HHS P30 CA013696 / NCI NIH HHS R01 EY024698 / NEI NIH HHS R01 AR059703 / NIAMS NIH HHS R01 EY026682 / NEI NIH HHS K08 EY020530 / NEI NIH HHS R01 EY024665 / NEI NIH HHS P30 EY019007 / NEI NIH HHS R21 AG050437 / NIA NIH HHS
- Language
- English
- Date published
- 2018
- Academic Unit
- Neurology; Stead Family Department of Pediatrics; Iowa Neuroscience Institute; Neuroscience and Pharmacology; Neurology (Pediatrics); Neurosurgery
- Record Identifier
- 9984070733002771
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