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Editing the genome of hiPSC with CRISPR/Cas9: disease models

The advent of human-induced pluripotent stem cell (hiPSC) technology has provided a unique opportunity to establish cellular models of disease from individual patients, and to study the effects of the underlying genetic aberrations upon multiple different cell types, many of which would not normally...

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Detalhes bibliográficos
Publicado no:Mamm Genome
Autor principal: Bassett, Andrew R.
Formato: Artigo
Idioma:Inglês
Publicado em: Springer US 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5569153/
https://ncbi.nlm.nih.gov/pubmed/28303292
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00335-017-9684-9
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