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mRNA and gene editing: Late breaking therapies in liver diseases

The efficient delivery of RNA molecules to restore the expression of a missing or inadequately functioning protein in a target cell and the intentional specific modification of the host genome using engineered nucleases represent therapeutic concepts that are revolutionizing modern medicine. The ini...

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Detalles Bibliográficos
Autores principales:	Zabaleta, Nerea, Torella, Laura, Weber, Nicholas D., Gonzalez‐Aseguinolaza, Gloria
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2022
Materias:	Reviews
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546265/ https://www.ncbi.nlm.nih.gov/pubmed/35243655 http://dx.doi.org/10.1002/hep.32441

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