REY, FEDERICA
REY, FEDERICA
Dipartimento di Scienze Biomediche e Cliniche
Gene expression analysis in subcutaneous adipose tissue reveals a predominant influence of lncRNAs during growth
2025 F. Rey, L. Messa, C. Berardo, A. Mauri, G. Zuccotti, C. Cereda, S. Carelli
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
Towards genomic-Newborn Screening: Technical feasibility of Exome Sequencing starting from dried blood spots
2024 A. Mauri, C. Berardo, D. Biganzoli, A. Meta, S. Benedetti, F. Rey, L. Messa, G.V. Zuccotti, S. Carelli, L. Alberti, 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
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
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
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
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
Ferritin nanoconjugates guide trastuzumab brain delivery to promote an antitumor response in murine HER2 + breast cancer brain metastasis
2023 M. Sevieri, S. Mazzucchelli, L. Barbieri, S. Garbujo, S. Carelli, A. Bonizzi, F. Rey, C. Recordati, M. Recchia, R. Allevi, L. Sitia, C. Morasso, P. Zerbi, D. Prosperi, F. Corsi, M. Truffi
Bone Marrow Mesenchymal Stem Cells Expanded Inside the Nichoid Micro-Scaffold: a Focus on Anti-Inflammatory Response
2023 B. Barzaghini, S. Carelli, L. Messa, F. Rey, M.A. Avanzini, E. Jacchetti, E. Maghraby, C. Berardo, G. Zuccotti, M.T. Raimondi, C. Cereda, V. Calcaterra, G. Pelizzo
Subcutaneous Adipose Tissue Transcriptome Highlights Specific Expression Profiles in Severe Pediatric Obesity: A Pilot Study
2023 C. Berardo, V. Calcaterra, A. Mauri, S. Carelli, L. Messa, F. Destro, F. Rey, E. Cordaro, G. Pelizzo, G. Zuccotti, C. Cereda
lncRNAs at the interplay between neurodegeneration and cancer: a role for MINCR
2023 C. Pandini, I. Cassotti, M. Garofalo, F. Rey, S. Carelli, C. Cereda, S. Gagliardi, P. Gandellini
Study of lncRNAs in Pediatric Neurological Diseases: Methods, Analysis of the State-of-Art and Possible Therapeutic Implications
2023 C. Pandini, F. Rey, C. Cereda, S. Carelli, P. Gandellini
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
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
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
COMPUTATIONAL AND BIOLOGICAL VALIDATION OF A NEW NICHOID SCAFFOLD OPTIMIZED FOR HUMAN MESENCHYMAL STEM CELLS
2022 B. Barzaghini, L. Messa, F. Rey, F. Fanizza, M. Antonella Sforazzini, G.V. Zuccotti, R. Osellame, G. Cerullo, E. Jacchetti, S. Carelli, M. Teresa Raimondi
Oxygen sensing in neurodegenerative diseases: current mechanisms, implication of transcriptional response and pharmacological modulation
2022 F. Rey, L. Messa, E. Maghraby, G. Casili, S. Ottolenghi, B. Barzaghini, M.T. Raimondi, C. Cereda, S. Cuzzocrea, G.V. Zuccotti, E. Esposito, I. Paterniti, S. Carelli