Enrico M. Surace, VMD PhD
Affiliations: | Telethon Institute of Genetics and Medicine, Italy |
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"Enrico Surace"
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Publications
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| Ferla R, Dell'Aquila F, Doria M, et al. (2023) Efficacy, pharmacokinetics, and safety in the mouse and primate retina of dual AAV vectors for Usher syndrome type 1B. Molecular Therapy. Methods & Clinical Development. 28: 396-411 |
| Tornabene P, Ferla R, Llado-Santaeularia M, et al. (2022) Therapeutic homology-independent targeted integration in retina and liver. Nature Communications. 13: 1963 |
| Tornabene P, Trapani I, Centrulo M, et al. (2021) Inclusion of a degron reduces levelsof undesired inteins after AAV-mediated proteinsplicing in the retina. Molecular Therapy. Methods & Clinical Development. 23: 448-459 |
| Marrocco E, Maritato R, Botta S, et al. (2021) Challenging Safety and Efficacy of Retinal Gene Therapies by Retinogenesis. International Journal of Molecular Sciences. 22 |
| Patrizi C, Llado M, Benati D, et al. (2021) Allele-specific editing ameliorates dominant retinitis pigmentosa in a transgenic mouse model. American Journal of Human Genetics. 108: 295-308 |
| Reynaud-Dulaurier R, Benegiamo G, Marrocco E, et al. (2020) Gene replacement therapy provides benefit in an adult mouse model of Leigh syndrome. Brain : a Journal of Neurology |
| Karali M, Guadagnino I, Marrocco E, et al. (2019) AAV-miR-204 Protects from Retinal Degeneration by Attenuation of Microglia Activation and Photoreceptor Cell Death. Molecular Therapy. Nucleic Acids. 19: 144-156 |
| Tornabene P, Trapani I, Minopoli R, et al. (2019) Intein-mediated protein trans-splicing expands adeno-associated virus transfer capacity in the retina. Science Translational Medicine. 11 |
| Botta S, de Prisco N, Marrocco E, et al. (2017) Targeting and silencing of rhodopsin by ectopic expression of the transcription factor KLF15. Jci Insight. 2 |
| Trapani I, Banfi S, Simonelli F, et al. (2015) Gene therapy of inherited retinal degenerations: prospects and challenges. Human Gene Therapy. 26: 193-200 |