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Free Radical Biology & Medicine|April 2, 2024
From powerhouse to regulator: The role of mitoepigenetics in mitochondrion-related cellular functions and human diseasesLuigi Donato, Domenico Mordà, Concetta Scimone, et al.Biomedicines|July 29, 2023
How Many Alzheimer-Perusini's Atypical Forms Do We Still Have to Discover?Luigi Donato, Domenico Mordà, Concetta Scimone, et al.Antioxidants (Basel, Switzerland)|April 16, 2020
Effects of A2E-Induced Oxidative Stress on Retinal Epithelial Cells: New Insights on Differential Gene Response and Retinal DystrophiesLuigi Donato, Rosalia D'Angelo, Simona Alibrandi, et al.Biomedicines|December 23, 2023
Bridging Retinal and Cerebral Neurodegeneration: A Focus on Crosslinks between Alzheimer-Perusini's Disease and Retinal DystrophiesLuigi Donato, Domenico Mordà, Concetta Scimone, et al.Antioxidants (Basel, Switzerland)|April 25, 2020
Transcriptome Analyses of lncRNAs in A2E-Stressed Retinal Epithelial Cells Unveil Advanced Links between Metabolic Impairments Related to Oxidative Stress and Retinitis PigmentosaLuigi Donato, Concetta Scimone, Simona Alibrandi, et al.International Journal of Molecular Medicine|March 15, 2017
Possible protective role of the ABCA4 gene c.1268A>G missense variant in Stargardt disease and syndromic retinitis pigmentosa in a Sicilian family: Preliminary dataRosalia D'Angelo, Luigi Donato, Isabella Venza, et al.Frontiers in Neurology|November 30, 2018
Two Novel KRIT1 and CCM2 Mutations in Patients Affected by Cerebral Cavernous Malformations: New Information on CCM2 PenetranceConcetta Scimone, Luigi Donato, Zoe Katsarou, et al.International Journal of Cardiology|July 29, 2008
Additive prognostic value of gamma-glutamyltransferase in coronary artery diseaseMichele Emdin, Claudio Passino, Claudio Michelassi, et al.Forensic Science International|August 9, 2019
Aged fingerprints for DNA profile: First report of successful typingCarlo Giovanni Romano, Rosaria Mangiaracina, Luigi Donato, et al.International Journal of Molecular Sciences|October 16, 2025
Computational Evidence for Digenic Contribution of AIPL1 and BBS2 Rare Variants in Inherited Retinal DystrophySimona Alibrandi, Concetta Scimone, Giorgia Abate, et al.Pageof 7