ESPOSITO, LETIZIA
ESPOSITO, LETIZIA
Dipartimento di Scienze Biomediche e Cliniche
NOVEL INSIGHTS ON ALLAN-HERNDON-DUDLEY SYNDROME: TRANSCRIPTIONAL PROFILING AND FUNCTIONAL CHARACTERIZATION OF THREE GENETIC VARIANTS IN SLC16A2 GENE
2025 L. Esposito
Transcriptional profiling and functional characterization of three genetic variants in SLC16A2 gene
2024 L. Esposito, F. Rey, E. Maghraby, L. Messa, M. Elli, F. Bruschi, G. Zuccotti, L. Alberti, D. Tonduti, S. Carelli, C. Cereda
Further insights into Allan-Herndon-Dudley syndrome: a novel SLC16A2 splice site variant
2024 L. Esposito, A. Mauri, F. Rey, E. Maghraby, B. Castellotti, G. Zuccotti, D. Tonduti, S. Carelli, C. Cereda
Transcriptional profiling and functional characterization of 3 patient-derived skin fibroblasts affected by Allan-Herndon-Dudley syndrome
2024 L. Esposito, F. Rey, E. Maghraby, L. Messa, M. Elli, F. Bruschi, G. Zuccotti, D. Tonduti, S. Carelli, C. Cereda
Novel frontiers in aicardi-goutières syndrome: association between a rnu7-1 variant and histone dysfunctions
2024 E. Maghraby, F. Rey, L. Esposito, M. Leone, A. Mauri, R. Allevi, S. Mazzucchelli, G. Zuccotti, D. Tonduti, S. Carelli, C. Cereda
Role of epigenetics and alterations in RNA metabolism in leukodystrophies
2024 F. Rey, L. Esposito, E. Maghraby, A. Mauri, C. Berardo, E. Bonaventura, D. Tonduti, S. Carelli, C. Cereda
Functional characterization and transcriptional profiling of fibroblasts from patients with mutations in SLC16A2 gene
2024 L. Esposito, F. Rey, E. Maghraby, L. Messa, F. Bruschi, G. Zuccotti, D. Tonduti, S. Carelli, C. Cereda
Effective lowering of α-synuclein expression by targeting G-quadruplex structures within the SNCA gene
2024 V. Pirota, F. Rey, L. Esposito, V. Fantini, C. Pandini, E. Maghraby, R. Di Gerlando, F. Doria, M. Mella, O. Pansarasa, P. Gandellini, M. Freccero, S. Carelli, C. Cereda
Further insights into Allan-Herndon-Dudley syndrome: characterization of two genetic variants in SLC16A2 gene
2023 L. Esposito, F. Rey, E. Maghraby, G. Zuccotti, D. Tonduti, S. Carelli, C. Cereda
SNCA-AS1, antisense transcript to the SNCA gene, regulates alpha-synuclein and synaptic modulation with possible implications in Parkinson’s Disease and aging.
2023 L. Esposito, F. Rey, E. Maghraby, L. Messa, C. Pandini, G. Zuccotti, S.C.C. Carelli
Redox Imbalance in Neurological Disorders in Adults and Children
2023 F. Rey, C. Berardo, E. Maghraby, A. Mauri, L. Messa, L. Esposito, G. Casili, S. Ottolenghi, E. Bonaventura, S. Cuzzocrea, G. Zuccotti, D. Tonduti, E. Esposito, I. Paterniti, C. Cereda, S. Carelli
Identification of a novel pathway in sporadic Amyotrophic Lateral Sclerosis mediated by the long non-coding RNA ZEB1-AS1
2023 F. Rey, E. Maghraby, L. Messa, L. Esposito, B. Barzaghini, C. Pandini, M. Bordoni, S. Gagliardi, L. Diamanti, M.T. Raimondi, M. Mazza, G. Zuccotti, S. Carelli, C. Cereda
Cancer Three-Dimensional Spheroids Mimic In Vivo Tumor Features, Displaying “Inner” Extracellular Vesicles and Vasculogenic Mimicry
2022 I. Giusti, G. Poppa, S. D'Ascenzo, L. Esposito, A.R. Vitale, G. Calvisi, V. Dolo
Tumor-Derived Extracellular Vesicles Activate Normal Human Fibroblasts to a Cancer-Associated Fibroblast-Like Phenotype, Sustaining a Pro-Tumorigenic Microenvironment
2022 I. Giusti, M. Di Francesco, G. Poppa, L. Esposito, S. D'Ascenzo, V. Dolo
Clinical potential of Extracellular Vesicles in Regenerative and Aesthetic Medicine
2022 G. Poppa, L. Esposito, V. Dolo, I. Giusti