ASGCT 2024 interview with CGT Live regarding the enveloped AAV platform
Video showcasing researchers from the MGB Gene and Cell Therapy Institute
Addgene plasmids from the Maguire lab including:
June 2021: We’ve place the plasmid for our ultra-efficient neurotropic capsid, AAV-F on Addgene!
Genscript Sponsored talk on our gene delivery technologies
ASGCT The Vector commentary describing our new AAV-F capsid.
ASGCT Conference Promotional Video
The Scientist article by Monique Brouillette describing exo-AAV for immune evasion
May 2019: Nice blog on addgene by Klaus Wanisch describing the exo-AAV system
MGH Research Institute story about our research
Article about therapies that cross the BBB in TheScientist.
Harvard Medical School press release regarding our work using exo-AAV for deafness gene therapy
Commentary on our article using exo-AAV to treat hereditary deafness
December 16, 2016
August 1, 2016
March 19, 2016
Funding from Cure Alzheimer's Fund to develop novel gene therapy for AD treatment
February 21, 2015
Article in Australian "the Saturday Paper" regarding the current state of gene therapy
February 9, 2015
Maguire Lab alum Zachary Fitzpatrick awardeda 2015 Gates Cambridge Scholarship
https://sites01.lsu.edu/wp/lovepurple/2015/02/06/fitzpatrick-gates-cambridge/
September 12, 2014
Link to article about CRISPR technology and potential for therapy.
May 23, 2014
At the 2014 American Society of Gene and Cell Therapy Meeting the Maguire Lab won "Outstanding Poster Presentation" on back to back nights for:
1. Poster 60. Vesicle-cloaked AAV resists neutralizing antibodies in vivo.
Zachary Fitzpatrick, Dakai Mu, Casey A. Maguire
2. Poster 297. Enhancing AAV9 transduction and multi-capsid packaging using extracellular vesicles.
Bence Gyorgy, Zachary Fitzpatrick, Dakai Mu, Casey A. Maguire