Hit-and-run programming of therapeutic cytoreagents using mRNA nanocarriers
Current widely used viral and electroporation methods for creating therapeutic cell-based products are complex and expensive. Here, the authors develop targeted mRNA nanocarriers that can transiently program gene expression by simply mixing them with cells, to improve their therapeutic potential.
Guardado en:
Autores principales: | H. F. Moffett, M. E. Coon, S. Radtke, S. B. Stephan, L. McKnight, A. Lambert, B. L. Stoddard, H. P. Kiem, M. T. Stephan |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/980299c002f4470893064c45e6cc2b18 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Genetic programming of macrophages to perform anti-tumor functions using targeted mRNA nanocarriers
por: F. Zhang, et al.
Publicado: (2019) -
In vitro-transcribed antigen receptor mRNA nanocarriers for transient expression in circulating T cells in vivo
por: N. N. Parayath, et al.
Publicado: (2020) -
Hit-and-run epigenetic editing prevents senescence entry in primary breast cells from healthy donors
por: Emily A. Saunderson, et al.
Publicado: (2017) -
Nanocarriers in the Enhancement of Therapeutic Efficacy of Natural Drugs
por: Xiuling Li, et al.
Publicado: (2021) -
Hard-hitting editorials
por: IFEX
Publicado: (1997)