A comparison of AAV-vector production methods for gene therapy and preclinical assessment
Abstract Adeno Associated Virus (AAV)-mediated gene expression in the brain is widely applied in the preclinical setting to investigate the therapeutic potential of specific molecular targets, characterize various cellular functions, and model central nervous system (CNS) diseases. In therapeutic ap...
Main Authors: | Marcus Davidsson, Matilde Negrini, Swantje Hauser, Alexander Svanbergsson, Marcus Lockowandt, Giuseppe Tomasello, Fredric P. Manfredsson, Andreas Heuer |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Publishing Group
2020-12-01
|
Series: | Scientific Reports |
Online Access: | https://doi.org/10.1038/s41598-020-78521-w |
Similar Items
-
Small scale adeno-associated virus-vector production for preclinical gene delivery based on chloroform precipitation
by: Marcus Davidsson, et al.
Published: (2022-01-01) -
Preclinical Assessment of Immune Responses to AAV (adeno-associated virus) Vectors
by: Etiena eBasner-Tschakarjan, et al.
Published: (2014-02-01) -
AAV-mediated gene therapy for choroideremia: preclinical studies in personalized models.
by: Vidyullatha Vasireddy, et al.
Published: (2013-01-01) -
Correction: AAV-Mediated Gene Therapy for Choroideremia: Preclinical Studies in Personalized Models.
by: Vidyullatha Vasireddy, et al.
Published: (2015-01-01) -
T Cell-Mediated Immune Responses to AAV and AAV Vectors
by: Hildegund C. J. Ertl
Published: (2021-04-01)