CRISPR/Cas9 Targeted Gene Editing and Cellular Engineering in Fanconi Anemia

The ability to rationally target disease-causing mutations has been made possible with programmable nucleases with the clustered, regularly interspaced short palindromic repeats/Cas9 system representing a facile platform for individualized gene-based medicine. In this study we employed footprint-fre...

詳細記述

保存先:
書誌詳細
出版年:Stem Cells Dev
主要な著者: Osborn, Mark J., Lonetree, Cara-lin, Webber, Beau R., Patel, Dharmeshkumar, Dunmire, Samantha, DeFeo, Anthony P., McElroy, Amber N., MacMillan, Margaret L., Wagner, John E., Blazar, Bruce R., Tolar, Jakub
フォーマット: Artigo
言語:Inglês
出版事項: Mary Ann Liebert, Inc. 2016
主題:
Original Research Reports
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC5035838/
https://ncbi.nlm.nih.gov/pubmed/27538887
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/scd.2016.0149
タグ: タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!

類似資料