Carolina Iodice

Telethon Institute Of Genetics And Medicine — Italy

Biochemistry, Genetics and Molecular Biology · Life Sciences

12h-index1.1kcitations18works0.02yr avg
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Research Topics

Retinal Development and Disorders(15), Virus-based gene therapy research(11), CRISPR and Genetic Engineering(7), interferon and immune responses(3), Erythropoietin and Anemia Treatment(2)

Publications18 total

Efficacy, pharmacokinetics, and safety in the mouse and primate retina of dual AAV vectors for Usher syndrome type 1B
Molecular Therapy — Methods & Clinical Development·2023· 24 citedOpen Access
Therapeutic homology-independent targeted integration in retina and liver
Nature Communications·2022· 42 citedOpen Access
Inclusion of a degron reduces levels of undesired inteins after AAV-mediated protein trans-splicing in the retina
Molecular Therapy — Methods & Clinical Development·2021· 23 citedOpen Access
Allele-specific editing ameliorates dominant retinitis pigmentosa in a transgenic mouse model
The American Journal of Human Genetics·2021· 47 citedOpen Access
Homology-Independent Targeted Integration in Photoreceptors
Investigative Ophthalmology & Visual Science·2019Open Access
Intein-mediated protein trans-splicing expands adeno-associated virus transfer capacity in the retina
Science Translational Medicine·2019· 177 citedOpen Access
High-Throughput Screening Identifies Kinase Inhibitors That Increase Dual Adeno-Associated Viral Vector Transduction <i>In Vitro</i> and in Mouse Retina
Human Gene Therapy·2018· 14 citedOpen Access
Improved dual AAV vectors with reduced expression of truncated proteins are safe and effective in the retina of a mouse model of Stargardt disease
Human Molecular Genetics·2015· 90 citedOpen Access
Optimization of dual AAV vectors for gene therapy of inherited retinal diseases
Investigative Ophthalmology & Visual Science·2015
500. Triple AAV Vectors Expand AAV Cargo Capacity in the Retina
Molecular Therapy·2015· 1 citedOpen Access
309. Optimization of Dual AAV Vectors for Gene Therapy of Inherited Retinal Diseases
Molecular Therapy·2015Open Access
Efficient gene delivery to the cone-enriched pig retina by dual AAV vectors
Gene Therapy·2014· 100 cited
Effective delivery of large genes to the retina by dual AAV vectors
EMBO Molecular Medicine·2013· 253 citedOpen Access
Non-erythropoietic Erythropoietin Derivatives Preserve Photoreceptors From Light-induced And Genetic Degeneration: Insights Into Erythropoietin Neuroprotective Mechanism
Investigative Ophthalmology & Visual Science·2011
Non-erythropoietic erythropoietin derivatives protect from light-induced and genetic photoreceptor degeneration
Human Molecular Genetics·2011· 38 citedOpen Access
AAV-Mediated Gene Replacement, Either Alone or in Combination with Physical and Pharmacological Agents, Results in Partial and Transient Protection from Photoreceptor Degeneration Associated with βPDE Deficiency
Investigative Ophthalmology & Visual Science·2011· 40 cited
Novel Adeno-Associated Virus Serotypes Efficiently Transduce Murine Photoreceptors
Journal of Virology·2007· 235 citedOpen Access
[Daily nutrient intake in hemodialysis].
PubMed·2004· 3 cited

Frequent Co-authors

Alberto Auricchio(16), Ivana Trapani(8), Pasqualina Colella(8), Settimio Rossi(7), Enrico Maria Surace(7), Elena Marrocco(6), Sonia de Simone(5), Francesca Simonelli(5), Andrea Sommella(4), Patrizia Tornabene(4), Renato Minopoli(4), Massimo Giunti(3), Roman Polishchuk(3), Miriam Centrulo(3), Fabio Dell’Aquila(3), Anna Manfredi(3), Umberto Di Vicino(3), Giulia Cesi(2), Mariacarmela Allocca(2), Mariangela Lupo(2)