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Cell Reports|May 10, 2018
The Assembly-Activating Protein Promotes Stability and Interactions between AAV's Viral Proteins to Nucleate Capsid AssemblyAnna C Maurer, Simon Pacouret, Ana Karla Cepeda Diaz, et al.
Molecular Therapy. Methods & Clinical Development|January 19, 2023
High-efficiency purification of divergent AAV serotypes using AAVX affinity chromatographyMichael Florea, Fotini Nicolaou, Simon Pacouret, et al.
Human Gene Therapy|January 13, 2018
Synthetic Adeno-Associated Viral Vector Efficiently Targets Mouse and Nonhuman Primate Retina In VivoLivia S Carvalho, Ru Xiao, Sarah J Wassmer, et al.
Blood|January 5, 2013
Classification of human natural killer cells based on migration behavior and cytotoxic responseBruno Vanherberghen, Per E Olofsson, Elin Forslund, et al.
Molecular Therapy. Methods & Clinical Development|September 2, 2024
Characterization of residual microRNAs in AAV vector batches produced in HEK293 mammalian cells and Sf9 insect cellsMagalie Penaud-Budloo, Emilie Lecomte, Quentin Lecomte, et al.
Cell Reports|August 4, 2015
In Silico Reconstruction of the Viral Evolutionary Lineage Yields a Potent Gene Therapy VectorEric Zinn, Simon Pacouret, Vadim Khaychuk, et al.
Molecular Therapy. Methods & Clinical Development|January 8, 2020
Cross-Packaging and Capsid Mosaic Formation in Multiplexed AAV LibrariesPauline F Schmit, Simon Pacouret, Eric Zinn, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 22, 2017
AAV-ID: A Rapid and Robust Assay for Batch-to-Batch Consistency Evaluation of AAV PreparationsSimon Pacouret, Mohammed Bouzelha, Rajani Shelke, et al.
Nature Cardiovascular Research|May 16, 2022
A High-Efficiency AAV for Endothelial Cell Transduction Throughout the Central Nervous SystemTrevor Krolak, Ken Y Chan, Luke Kaplan, et al.
Chemical Science|June 4, 2021
Chemical modification of the adeno-associated virus capsid to improve gene deliveryMathieu Mével, Mohammed Bouzelha, Aurélien Leray, et al.
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