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Frontiers in Cell and Developmental Biology|February 16, 2026
Alternative splicing regulates PACC1 function and promotes acidosis-induced cytotoxicitySerena Tamburro, Giulia Gorrieri, Niccolò Callegari, et al.
Stem Cell Research|February 13, 2024
Generation of two iPSC lines from Mowat-Wilson syndrome patients carrying heterozygous ZEB2 mutationsGiulia Gorrieri, Serena Tamburro, Simona Baldassari, et al.
Stem Cell Research|October 21, 2023
Generation of an induced pluripotent stem cell line (IGGi002A) from nasal cells of a cystic fibrosis patient homozygous for the G542X-CFTR mutationMichał Dębczyński, Damian Mojsak, Serena Tamburro, et al.
Neurobiology of Disease|December 1, 2025
Modeling Mowat-Wilson syndrome with patient iPSCs reveals transcriptional and phenotypic defects in neural progenitorsIlaria Musante, Giulia Gorrieri, Serena Tamburro, et al.
Stem Cell Reviews and Reports|January 31, 2025
Optimization of Transcription Factor-Driven Neuronal Differentiation from Human Induced Pluripotent Stem Cells for Disease Modelling and Drug ScreeningMartina Servetti, Martino Caramia, Giulia Parodi, et al.
Human Mutation|April 14, 2025
Somatic Double Inactivation of NF1 Associated with NF1-Related Pectus Excavatum DeformityCristina Chelleri, Marcello Scala, Patrizia De Marco, et al.
Frontiers in Molecular Neuroscience|April 23, 2024
Allelic heterogeneity and abnormal vesicle recycling in PLAA-related neurodevelopmental disordersMichele Iacomino, Nadia Houerbi, Sara Fortuna, et al.
American Journal of Human Genetics|February 22, 2024
De novo variants in DENND5B cause a neurodevelopmental disorderMarcello Scala, Valeria Tomati, Matteo Ferla, et al.
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