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Tissue Eng Part C Methods ; 25(3): 168-175, 2019 03.
Artículo en Inglés | MEDLINE | ID: mdl-30747044

RESUMEN

IMPACT STATEMENT: Cell lines represent convenient models to elucidate specific causes of multigenetic and pluricausal diseases, to test breakthrough regenerative technologies. Most commonly used cell lines surpass diploid cells in their accessibility for delivery of large DNA molecules and genome editing, but the main obstacles for obtaining cell models with knockout-targeted protein from aneuploid cells are multiple allele copies and karyotype/phenotype heterogeneity. In the study, we report an original approach to CRISPR-/Cas9-mediated genome modification of aneuploid cell cultures to create functional cell models, achieving highly efficient targeted protein knockout and avoiding "clonal effect" (for the first time to our knowledge).


Asunto(s)
Aneuploidia , Sistemas CRISPR-Cas , Edición Génica , Técnicas de Inactivación de Genes/normas , Genes/genética , Animales , Células HeLa , Células Hep G2 , Humanos , Ratones , Células 3T3 NIH
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