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A Bioengineered In Vitro Model to Assess AAV-Based Gene Therapies for Cyclic GMP-Related Disorders

The emergence of efficient viral vectors derived from adeno-associated viruses (AAV) has led many groups to develop gene therapies for inherited monogenic diseases, such as retinal dystrophies. To evaluate the potency of new gene therapy vectors in a preclinical context, it is common to use animal m...

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Detalles Bibliográficos
Autores principales: Pavlou, Marina, Babutzka, Sabrina, Michalakis, Stylianos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9101586/
https://www.ncbi.nlm.nih.gov/pubmed/35562929
http://dx.doi.org/10.3390/ijms23094538

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