Publications by authors named "Lucio Nitsch"

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[Corrigendum] Lithium chloride induces mesenchymal‑to‑epithelial reverting transition in primary colon cancer cell cultures.
Valeria Costabile, Francesca Duraturo, Paolo Delrio, Daniela Rega, Ugo Pace, Lucio Nitsch

Int J Oncol· November 2025

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Genetics and Molecular Basis of Congenital Heart Defects in Down Syndrome: Role of Extracellular Matrix Regulation.
Nunzia Mollo, Roberta Scognamiglio, Anna Conti, Simona Paladino, Lucio Nitsch

Int J Mol Sci· February 2023

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Down Syndrome Fetal Fibroblasts Display Alterations of Endosomal Trafficking Possibly due to SYNJ1 Overexpression.
Laura De Rosa, Dominga Fasano, Lucrezia Zerillo, Valeria Valente, Antonella Izzo, Lucio Nitsch

Front Genet· May 2022

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Overexpression of the Hsa21 Transcription Factor RUNX1 Modulates the Extracellular Matrix in Trisomy 21 Cells.
Nunzia Mollo, Miriam Aurilia, Roberta Scognamiglio, Lucrezia Zerillo, Rita Cicatiello, Lucio Nitsch

Front Genet· March 2022

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Human Trisomic iPSCs from Down Syndrome Fibroblasts Manifest Mitochondrial Alterations Early during Neuronal Differentiation.
Nunzia Mollo, Matteo Esposito, Miriam Aurilia, Roberta Scognamiglio, Rossella Accarino, Lucio Nitsch

Biology (Basel)· June 2021

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Clinical Phenotype, Immunological Abnormalities, and Genomic Findings in Patients with DiGeorge Spectrum Phenotype without 22q11.2 Deletion.
Emilia Cirillo, Maria Rosaria Prencipe, Giuliana Giardino, Roberta Romano, Giulia Scalia, Lucio Nitsch

J Allergy Clin Immunol Pract· October 2020

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Corrigendum: Pioglitazone Improves Mitochondrial Organization and Bioenergetics in Down Syndrome Cells.
Nunzia Mollo, Maria Nitti, Lucrezia Zerillo, Deriggio Faicchia, Teresa Micillo, Lucio Nitsch

Front Genet· July 2020

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The centrosomal/basal body protein OFD1 is required for microtubule organization and cell cycle progression.
Mariaevelina Alfieri, Daniela Iaconis, Roberta Tammaro, Lucia Perone, Gaetano Calì, Lucio Nitsch

Tissue Cell· June 2020

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Targeting Mitochondrial Network Architecture in Down Syndrome and Aging.
Nunzia Mollo, Rita Cicatiello, Miriam Aurilia, Roberta Scognamiglio, Rita Genesio, Lucio Nitsch

Int J Mol Sci· April 2020

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Microdeletion of pseudogene chr14.232.a affects LRFN5 expression in cells of a patient with autism spectrum disorder.
Gerarda Cappuccio, Sergio Attanasio, Marianna Alagia, Margherita Mutarelli, Roberta Borzone, Lucio Nitsch

Eur J Hum Genet· September 2019

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PERK-Mediated Unfolded Protein Response Activation and Oxidative Stress in PARK20 Fibroblasts.
Giuseppina Amodio, Ornella Moltedo, Dominga Fasano, Lucrezia Zerillo, Marco Oliveti, Lucio Nitsch

Front Neurosci· June 2019

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Pioglitazone Improves Mitochondrial Organization and Bioenergetics in Down Syndrome Cells.
Nunzia Mollo, Maria Nitti, Lucrezia Zerillo, Deriggio Faicchia, Teresa Micillo, Lucio Nitsch

Front Genet· June 2019

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Chromosomal Microarray Analysis versus Karyotyping in Fetuses with Increased Nuchal Translucency.
Rita Cicatiello, Piero Pignataro, Antonella Izzo, Nunzia Mollo, Lucia Pezone, Lucio Nitsch

Med Sci (Basel)· February 2019

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Prenatally diagnosed distal 16p11.2 microdeletion with a novel association with congenital diaphragmatic hernia: a case report.
Rita Genesio, Giuseppe Maria Maruotti, Gabriele Saccone, Angela Mormile, Anna Conti, Lucio Nitsch

Clin Case Rep· April 2018

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Alteration of endosomal trafficking is associated with early-onset parkinsonism caused by SYNJ1 mutations.
Dominga Fasano, Silvia Parisi, Giovanna Maria Pierantoni, Anna De Rosa, Marina Picillo, Lucio Nitsch

Cell Death Dis· March 2018

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Mitochondrial dysfunction in down syndrome: molecular mechanisms and therapeutic targets.
Antonella Izzo, Nunzia Mollo, Maria Nitti, Simona Paladino, Gaetano Calì, Lucio Nitsch

Mol Med· March 2018

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A novel SHANK3 interstitial microdeletion in a family with intellectual disability and brain MRI abnormalities resembling Unidentified Bright Objects.
Gaetano Terrone, Giuseppina Vitiello, Rita Genesio, Alessandra D'Amico, Floriana Imperati, Lucio Nitsch

Eur J Paediatr Neurol· November 2017

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Overexpression of Chromosome 21 miRNAs May Affect Mitochondrial Function in the Hearts of Down Syndrome Fetuses.
Antonella Izzo, Rosanna Manco, Tiziana de Cristofaro, Ferdinando Bonfiglio, Rita Cicatiello, Lucio Nitsch

Int J Genomics· September 2017

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DiGeorge-like syndrome in a child with a 3p12.3 deletion involving MIR4273 gene born to a mother with gestational diabetes mellitus.
Emilia Cirillo, Giuliana Giardino, Vera Gallo, Giovanni Galasso, Roberta Romano, Lucio Nitsch

Am J Med Genet A· July 2017

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Alterations in metabolic patterns have a key role in diagnosis and progression of primrose syndrome.
Alberto Casertano, Paolo Fontana, Raoul C Hennekam, Marco Tartaglia, Rita Genesio, Lucio Nitsch

Am J Med Genet A· July 2017

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Regulation of sub-compartmental targeting and folding properties of the Prion-like protein Shadoo.
Anna Pepe, Rosario Avolio, Danilo Swann Matassa, Franca Esposito, Lucio Nitsch

Sci Rep· June 2017

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Metformin restores the mitochondrial network and reverses mitochondrial dysfunction in Down syndrome cells.
Antonella Izzo, Maria Nitti, Nunzia Mollo, Simona Paladino, Claudio Procaccini, Lucio Nitsch

Hum Mol Genet· March 2017

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Mulibrey nanism: Two novel mutations in a child identified by Array CGH and DNA sequencing.
Enza Mozzillo, Carla Cozzolino, Rita Genesio, Daniela Melis, Giulia Frisso, Lucio Nitsch

Am J Med Genet A· August 2016

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Erratum to: In vivo role of different domains and of phosphorylation in the transcription factor Nkx2-1.
Daniel Silberschmidt, Alina Rodriguez-Mallon, Prathiba Mithboakar, Gaetano Calì, Elena Amendola, Lucio Nitsch

BMC Dev Biol· August 2016

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New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants.
Gerarda Cappuccio, Francesco Vitiello, Alberto Casertano, Paolo Fontana, Rita Genesio, Lucio Nitsch

Ital J Pediatr· April 2016

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