Hirsch, Matthew L.
University of North Carolina at Chapel Hill
14 papers on CoChatORCID 0000-0003-2062-0744
Most cited papers
- Verified
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 virus serotype
Ellis, B. L., Hirsch, M. L., Barker, J. C., Connelly, J. P., Steininger, R. J., & Porteus, M. H. (2013) · Virology Journal
Virus-based gene therapy researchRNA Interference and Gene Delivery
Cited by 252
- Verified
Proteasome Inhibitors Enhance Gene Delivery by AAV Virus Vectors Expressing Large Genomes in Hemophilia Mouse and Dog Models: A Strategy for Broad Clinical Application
Monahan, P. E., Lothrop, C. D., Sun, J., Hirsch, M. L., Kafri, T., Kantor, B., Sarkar, R., Tillson, D. M., Elia, J. R., & Samulski, R. J. (2010) · Molecular Therapy
Virus-based gene therapy researchHemophilia Treatment and Research
Cited by 125
- Verified
Double-stranded RNA innate immune response activation from long-term adeno-associated virus vector transduction
Shao, W., Earley, L. F., Chai, Z., Chen, X., Sun, J., He, T., Deng, M., Hirsch, M. L., Ting, J., Samulski, R. J., et al. (2018) · JCI Insight
Virus-based gene therapy researchRNA Interference and Gene Delivery
Cited by 119
- Verified
Adeno-Associated Virus Serotype-Specific Inverted Terminal Repeat Sequence Role in Vector Transgene Expression
Earley, L. F., Conatser, L. M., Lue, V. M., Dobbins, A. L., Li, C., Hirsch, M. L., & Samulski, R. J. (2020) · Human Gene Therapy
Virus-based gene therapy researchRNA Interference and Gene Delivery
Cited by 111
- Verified
Single amino acid modification of adeno-associated virus capsid changes transduction and humoral immune profiles
Li, C., Diprimio, N., Bowles, D. E., Hirsch, M. L., Monahan, P. E., Asokan, A., Rabinowitz, J., Agbandje-McKenna, M., & Samulski, R. J. (2012) · Journal of Virology
Virus-based gene therapy researchRNA Interference and Gene Delivery
Cited by 96
- Verified
Oversized AAV Transductifon Is Mediated via a DNA-PKcs-independent, Rad51C-dependent Repair Pathway
Hirsch, M. L., Li, C., Bellon, I., Yin, C., Chavala, S., Pryadkina, M., Richard, I., & Samulski, R. J. (2013) · Molecular Therapy
Virus-based gene therapy researchRNA Interference and Gene Delivery
Cited by 62
- Verified
A comparison of AAV strategies distinguishes overlapping vectors for efficient systemic delivery of the 6.2 kb Dysferlin coding sequence
Pryadkina, M., Lostal, W., Bourg, N., Charton, K., Roudaut, C., Hirsch, M. L., & Richard, I. (2015) · Molecular Therapy - Methods & Clinical Development
Virus-based gene therapy researchNeurogenetic and Muscular Disorders Research
Cited by 53
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Viral Single-Strand DNA Induces p53-Dependent Apoptosis in Human Embryonic Stem Cells
Hirsch, M. L., Fagan, B. M., Dumitru, R., Bower, J. J., Yadav, S., Porteus, M. H., Pevny, L. H., & Samulski, R. J. (2011) · PLoS ONE
Virus-based gene therapy researchDNA Repair Mechanisms
Cited by 53
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Serotype survey of AAV gene delivery via subconjunctival injection in mice
Song, L., Llanga, T., Conatser, L. M., Zaric, V., Gilger, B. C., & Hirsch, M. L. (2018) · Gene Therapy
Virus-based gene therapy researchRNA Interference and Gene Delivery
Cited by 50
- Verified
Identification and Validation of Small Molecules That Enhance Recombinant Adeno-associated Virus Transduction following High-Throughput Screens
Nicolson, S. C., Li, C., Hirsch, M. L., Setola, V., & Samulski, R. J. (2016) · Journal of Virology
Virus-based gene therapy researchRNA Interference and Gene Delivery
Cited by 48
- Verified
Development of patient-specific AAV vectors after neutralizing antibody selection for enhanced muscle gene transfer
Li, C., Wu, S., Albright, B., Hirsch, M., Li, W., Tseng, Y.-S., Agbandje-McKenna, M., McPhee, S., Asokan, A., & Samulski, R. J. (2016) · Molecular Therapy
Virus-based gene therapy researchRNA Interference and Gene Delivery
Cited by 48
- Verified
Adeno-associated virus inverted terminal repeats stimulate gene editing
Hirsch, M. L. (2015) · Gene Therapy
CRISPR and Genetic EngineeringVirus-based gene therapy research
Cited by 32
- Verified
Inhibition of antigen presentation during AAV gene therapy using virus peptides
Shao, W., Chen, X., Samulski, R. J., Hirsch, M. L., & Li, C. (2018) · Human Molecular Genetics
Virus-based gene therapy researchImmunotherapy and Immune Responses
Cited by 17
- Verified
Ocular tolerability and immune response to corneal intrastromal AAV-IDUA gene therapy in New Zealand white rabbits
Song, L., Bower, J. J., Llanga, T., Salmon, J. H., Hirsch, M. L., & Gilger, B. C. (2020) · Molecular Therapy - Methods & Clinical Development
Virus-based gene therapy researchLysosomal Storage Disorders Research
Cited by 14
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