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Molecular Therapy : the Journal of the American Society of Gene Therapy|August 11, 2016
Therapeutic Potential of Immunoproteasome Inhibition in Duchenne Muscular DystrophyAndrea Farini, Clementina Sitzia, Barbara Cassani, et al.
Journal of Personalized Medicine|November 19, 2020
Inhibition of 37/67kDa Laminin-1 Receptor Restores APP Maturation and Reduces Amyloid-β in Human Skin Fibroblasts from Familial Alzheimer's DiseaseAntaripa Bhattacharya, Antonella Izzo, Nunzia Mollo, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 29, 2015
Upregulation of the N-formyl Peptide receptors in scleroderma fibroblasts fosters the switch to myofibroblastsFrancesca Wanda Rossi, Filomena Napolitano, Ada Pesapane, et al.
International Journal of Molecular Sciences|April 3, 2021
Rare Variants in Autophagy and Non-Autophagy Genes in Late-Onset Pompe Disease: Suggestions of Their Disease-Modifying Role in Two Italian FamiliesFilomena Napolitano, Giorgia Bruno, Chiara Terracciano, et al.
Neuropathology and Applied Neurobiology|January 4, 2021
Novel autophagic vacuolar myopathies: Phenotype and genotype featuresFilomena Napolitano, Chiara Terracciano, Giorgia Bruno, et al.
Journal of the Neurological Sciences|August 6, 2025
Serum miRNAs as biomarkers in Neurofibromatosis 1: New promising findingsFilomena Napolitano, Gianmarco Abbadessa, Milena Dell'Aquila, et al.
Journal of Cellular Physiology|December 8, 2017
Vacuolated PAS-positive lymphocytes as an hallmark of Pompe disease and other myopathies related to impaired autophagyAngelo Pascarella, Chiara Terracciano, Olimpia Farina, et al.
Clinical Chemistry and Laboratory Medicine|November 24, 2023
Estimation of the reference values and decision limits for growth hormone in newborns using dried blood spotsMatteo Vidali, Federico Giacchetti, Andrea Sangiorgio, et al.
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