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Collateral damage and CRISPR genome editing

The simplicity and the versatility of clustered regularly interspaced short palindromic repeats/CRISPR-associated protein (CRISPR-Cas) systems have enabled the genetic modification of virtually every organism and offer immense therapeutic potential for the treatment of human disease. Although these...

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Publicat a:PLoS Genet
Autors principals: Thomas, Mark, Burgio, Gaetan, Adams, David J., Iyer, Vivek
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2019
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6417652/
https://ncbi.nlm.nih.gov/pubmed/30870431
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1007994
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