Therapeutic Applications of Adeno-Associated Virus (AAV) Gene Transfer of HLA-G in the Eye

por Gilger, Brian C., Hirsch, Matthew L.
Publicado 2022

Adeno-Associated Virus Mediated Gene Therapy for Corneal Diseases

por Bastola, Prabhakar, Song, Liujiang, Gilger, Brian C., Hirsch, Matthew L.
Publicado 2020

Harnessing the Natural Biology of Adeno-Associated Virus to Enhance the Efficacy of Cancer Gene Therapy

por Bower, Jacquelyn J., Song, Liujiang, Bastola, Prabhakar, Hirsch, Matthew L.
Publicado 2021

AAV Recombineering with Single Strand Oligonucleotides

por Hirsch, Matthew L., Storici, Francesca, Li, Chengwen, Choi, Vivian W., Samulski, R. Jude
Publicado 2009

A comparison of AAV strategies distinguishes overlapping vectors for efficient systemic delivery of the 6.2 kb Dysferlin coding sequence

por Pryadkina, Marina, Lostal, William, Bourg, Nathalie, Charton, Karine, Roudaut, Carinne, Hirsch, Matthew L, Richard, Isabelle
Publicado 2015

Direct Interaction of Human Serum Proteins with AAV Virions to Enhance AAV Transduction: Immediate Impact on Clinical Applications

por Wang, Mei, Sun, Junjiang, Crosby, Ashley, Woodard, Kenton, Hirsch, Matthew L., Samulski, R. Jude, Li, Chengwen
Publicado 2016

Ocular Tolerability and Immune Response to Corneal Intrastromal AAV-IDUA Gene Therapy in New Zealand White Rabbits

por Song, Liujiang, Bower, Jacquelyn J., Llanga, Telmo, Salmon, Jacklyn H., Hirsch, Matthew L., Gilger, Brian C.
Publicado 2020

A survey of ex vivo/in vitro transduction efficiency of mammalian primary cells and cell lines with Nine natural adeno-associated virus (AAV1-9) and one engineered adeno-associated...

por Ellis, Brian L, Hirsch, Matthew L, Barker, Jenny C, Connelly, Jon P, Steininger, Robert J, Porteus, Matthew H
Publicado 2013

Adeno-Associated Virus Vector Mediated Delivery of the HBV Genome Induces Chronic Hepatitis B Virus Infection and Liver Fibrosis in Mice

por Ye, Lei, Yu, Haisheng, Li, Chengwen, Hirsch, Matthew L., Zhang, Liguo, Samulski, R. Jude, Li, Wuping, Liu, Zhong
Publicado 2015

Three-dimensional multipotent progenitor cell aggregates for expansion, osteogenic differentiation and “in vivo” tracing with AAV vector serotype 6

por Ferreira, Joäo R., Hirsch, Matthew L., Zhang, Li, Park, Yonsil, Samulski, R. Jude, Hu, Wei-Shou, Ko, Ching-Chang
Publicado 2012

AAV-mediated expression of HLA-G1/5 reduces severity of experimental autoimmune uveitis

por Crabtree, Elizabeth, Song, Liujiang, Llanga, Telmo, Bower, Jacquelyn J., Cullen, Megan, Salmon, Jacklyn H., Hirsch, Matthew L., Gilger, Brian C.
Publicado 2019

Viral Single-Strand DNA Induces p53-Dependent Apoptosis in Human Embryonic Stem Cells

por Hirsch, Matthew L., Fagan, B. Matthew, Dumitru, Raluca, Bower, Jacquelyn J., Yadav, Swati, Porteus, Matthew H., Pevny, Larysa H., Samulski, R. Jude
Publicado 2011

AAV vector-meditated expression of HLA-G reduces injury-induced corneal vascularization, immune cell infiltration, and fibrosis

por Hirsch, Matthew L., Conatser, Laura M., Smith, Sara M., Salmon, Jacklyn H., Wu, Jerry, Buglak, Nicholas E., Davis, Rich, Gilger, Brian C.
Publicado 2017

AAV Gene Therapy for MPS1-associated Corneal Blindness

por Vance, Melisa, Llanga, Telmo, Bennett, Will, Woodard, Kenton, Murlidharan, Giridhar, Chungfat, Neil, Asokan, Aravind, Gilger, Brian, Kurtzberg, Joanne, Samulski, R. Jude, Hirsch, Matthew L.
Publicado 2016

Inhibition of experimental autoimmune uveitis by intravitreal AAV-Equine-IL10 gene therapy

por Crabtree, Elizabeth, Uribe, Katy, Smith, Sara M., Roberts, Darby, Salmon, Jacklyn H., Bower, Jacquelyn J., Song, Liujiang, Bastola, Prabhakar, Hirsch, Matthew L., Gilger, Brian C.
Publicado 2022

Hip region muscular dystrophy and emergence of motor deficits in dysferlin‐deficient Bla/J mice

por Nagy, Nadia, Nonneman, Randal J., Llanga, Telmo, Dial, Catherine F., Riddick, Natallia V., Hampton, Tom, Moy, Sheryl S., Lehtimäki, Kimmo K., Ahtoniemi, Toni, Puoliväli, Jukka, Windish, Hillarie, Albrecht, Douglas, Richard, Isabelle, Hirsch, Matthew L.
Publicado 2017

Integration of a CD19 CAR into the TCR Alpha Chain Locus Streamlines Production of Allogeneic Gene-Edited CAR T Cells

por MacLeod, Daniel T., Antony, Jeyaraj, Martin, Aaron J., Moser, Rachel J., Hekele, Armin, Wetzel, Keith J., Brown, Audrey E., Triggiano, Melissa A., Hux, Jo Ann, Pham, Christina D., Bartsevich, Victor V., Turner, Caitlin A., Lape, Janel, Kirkland, Samantha, Beard, Clayton W., Smith, Jeff, Hirsch, Matthew L., Nicholson, Michael G., Jantz, Derek, McCreedy, Bruce
Publicado 2017