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International Journal of Molecular Sciences|February 11, 2023
Genetics and Molecular Basis of Congenital Heart Defects in Down Syndrome: Role of Extracellular Matrix RegulationNunzia Mollo, Roberta Scognamiglio, Anna Conti, et al.
BJR Open|July 14, 2023
Pictorial guide for variants of Covid-19: CT imaging and interpretationGiacomo Bonito, Valeria Martinelli, Francesco Vullo, et al.
La Radiologia Medica|August 10, 2021
Quantitative CT texture analysis in predicting PD-L1 expression in locally advanced or metastatic NSCLC patientsStefano Bracci, Miriam Dolciami, Claudio Trobiani, et al.
Cell Cycle (Georgetown, Tex.)|February 19, 2016
Hmga1 null mouse embryonic fibroblasts display downregulation of spindle assembly checkpoint gene expression associated to nuclear and karyotypic abnormalitiesGiovanna Maria Pierantoni, Andrea Conte, Cinzia Rinaldo, et al.
Journal of Cellular Physiology|November 25, 2015
Rab7 Regulates CDH1 Endocytosis, Circular Dorsal Ruffles Genesis, and Thyroglobulin Internalization in a Thyroid Cell LineAnna Mascia, Flaviana Gentile, Antonella Izzo, et al.
International Journal of Molecular Sciences|May 6, 2020
Targeting Mitochondrial Network Architecture in Down Syndrome and AgingNunzia Mollo, Rita Cicatiello, Miriam Aurilia, et al.
Cancer Cell International|December 14, 2019
PAX8 expression in high-grade serous ovarian cancer positively regulates attachment to ECM via Integrin β3Amata Amy Soriano, Tiziana de Cristofaro, Tina Di Palma, et al.
Frontiers in Genetics|March 31, 2022
Overexpression of the Hsa21 Transcription Factor RUNX1 Modulates the Extracellular Matrix in Trisomy 21 CellsNunzia Mollo, Miriam Aurilia, Roberta Scognamiglio, et al.
Biochimica Et Biophysica Acta. Molecular Cell Research|July 9, 2025
Modulation of mitochondrial quality control through autophagic pathway in familial Alzheimer's diseaseAdriana Limone, Clelia Di Napoli, Giusy De Rosa, et al.
Stem Cell Research|April 2, 2021
Generation of an iPSC line (UNINAi001-A) from a girl with neonatal-onset epilepsy and non-syndromic intellectual disability carrying the homozygous KCNQ3 p.PHE534ILEfs*15 variant and of an iPSC line (UNINAi002-A) from a non-carrier, unaffected brotherElena Longobardi, Francesco Miceli, Agnese Secondo, et al.
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