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Autor:
Jessica M. Porter, Mackenzi S. Oswald, Anjali Sharma, Shanan Emmanuel, Austin Kansol, Antonette Bennett, Robert McKenna, Jason G. Smith
Publikováno v:
Journal of Virology. 97
The ability of adeno-associated viruses (AAVs) to infect and deliver genetic material to a range of cell types makes them favorable gene therapy vectors. However, AAV vectors encounter a wide variety of host immune factors throughout the body, which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3529a4f012a721abe192decf75733e57
https://doi.org/10.1128/jvi.00060-23
https://doi.org/10.1128/jvi.00060-23
