Publications by authors named "Maria Falzarano"

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Modulation of the JAK2-STAT3 pathway promotes expansion and maturation of human iPSC-derived myogenic progenitor cells.
Luca Caputo, Cedomir Stamenkovic, Matthew T Tierney, Alessandra Cecchini, Monica Nicolau, Maria Sofia Falzarano

Stem Cell Reports· November 2025

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External validation of a predictive model for post-treatment persistent disease by I whole-body scintigraphy in patients with differentiated thyroid cancer.
Carmela Nappi, Rosario Megna, Emilia Zampella, Fabio Volpe, Leandra Piscopo, Maria Falzarano

Eur J Nucl Med Mol Imaging· July 2025

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Prognostic value of myocardial flow reserve by PET imaging in patients with suspected coronary artery disease: A systematic review and meta-analysis.
Adriana D'Antonio, Roberta Assante, Emilia Zampella, Valeria Cantoni, Roberta Green, Maria Falzarano

Int J Cardiol Heart Vasc· June 2025

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mRNA Profile in Brain Tissues from a Rett Syndrome Patient and Three Human Controls: Mutated Allele Preferential Transcription and In Situ RNA Mapping.
Martina Mietto, Silvia Montanari, Maria Sofia Falzarano, Elisa Manzati, Paola Rimessi

Biomolecules· May 2025

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Modulation of the JAK2-STAT3 pathway promotes expansion and maturation of human iPSCs-derived myogenic progenitor cells.
Luca Caputo, Cedomir Stamenkovic, Matthew T Tierney, Maria Sofia Falzarano, Rhonda Bassel-Duby

bioRxiv· December 2024

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Trabecular bone score assessed by dual-energy X ray absorption predicts vertebral fractures in HIV infected young adults.
Teresa Mannarino, Adriana D'Antonio, Simona Mercinelli, Maria Falzarano, Federica Volpicelli

Bone Rep· September 2024

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mRNA in situ hybridization exhibits unbalanced nuclear/cytoplasmic dystrophin transcript repartition in Duchenne myogenic cells and skeletal muscle biopsies.
Maria Sofia Falzarano, Martina Mietto, Fernanda Fortunato, Marianna Farnè, Fernanda Martini

Sci Rep· September 2023

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Efficacy of Empirical Radioiodine Therapy in Patients with Differentiated Thyroid Cancer and Elevated Serum Thyroglobulin without Evidence of Structural Disease: A Propensity Score Analysis.
Leandra Piscopo, Emilia Zampella, Fabio Volpe, Valeria Gaudieri, Carmela Nappi, Maria Falzarano

Cancers (Basel)· August 2023

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Tracers for Cardiac Imaging: Targeting the Future of Viable Myocardium.
Carmela Nappi, Mariarosaria Panico, Maria Falzarano, Carlo Vallone, Andrea Ponsiglione

Pharmaceutics· May 2023

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Intramedullary Spinal Cord Metastases from Differentiated Thyroid Cancer, a Case Report.
Fabio Volpe, Leandra Piscopo, Mariarosaria Manganelli, Maria Falzarano, Federica Volpicelli

Life (Basel)· June 2022

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RNA-seq in DMD urinary stem cells recognized muscle-related transcription signatures and addressed the identification of atypical mutations by whole-genome sequencing.
Maria S Falzarano, Andrea Grilli, Silvia Zia, Mingyan Fang, Rachele Rossi

HGG Adv· January 2022

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Dystrophin involvement in peripheral circadian SRF signalling.
Corinne A Betts, Aarti Jagannath, Tirsa LE van Westering, Melissa Bowerman, Subhashis Banerjee, Maria Sofia Falzarano

Life Sci Alliance· October 2021

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Urine-Derived Stem Cells Express 571 Neuromuscular Disorders Causing Genes, Making Them a Potential Model for Rare Genetic Diseases.
Maria Sofia Falzarano, Rachele Rossi, Andrea Grilli, Mingyan Fang, Hana Osman

Front Physiol· October 2021

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Circadian Genes as Exploratory Biomarkers in DMD: Results From Both the Mouse Model and Patients.
Rachele Rossi, Maria Sofia Falzarano, Hana Osman, Annarita Armaroli, Chiara Scotton

Front Physiol· July 2021

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Chitosan-Shelled Nanobubbles Irreversibly Encapsulate Morpholino Conjugate Antisense Oligonucleotides and Are Ineffective for Phosphorodiamidate Morpholino-Mediated Gene Silencing of .
Maria Sofia Falzarano, Monica Argenziano, Anne Chalotte Marsollier, Virginie Mariot, Davide Rossi

Nucleic Acid Ther· June 2021

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Innovative Therapeutic Approaches for Duchenne Muscular Dystrophy.
Fernanda Fortunato, Rachele Rossi, Maria Sofia Falzarano, Alessandra Ferlini

J Clin Med· February 2021

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Tumor Necrosis Factor Receptor SF10A (TNFRSF10A) SNPs Correlate With Corticosteroid Response in Duchenne Muscular Dystrophy.
Chiara Passarelli, Rita Selvatici, Alberto Carrieri, Francesca Romana Di Raimo, Maria Sofia Falzarano

Front Genet· July 2020

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The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study.
Marcella Neri, Rachele Rossi, Cecilia Trabanelli, Antonio Mauro, Rita Selvatici, Maria Sofia Falzarano

Front Genet· March 2020

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Nanodiagnostics and Nanodelivery Applications in Genetic Alterations.
Maria Sofia Falzarano, Cristina Flesia, Roberta Cavalli, Caterina Guiot, Alessandra Ferlini

Curr Pharm Des· October 2019

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Urinary Stem Cells as Tools to Study Genetic Disease: Overview of the Literature.
Maria Sofia Falzarano, Alessandra Ferlini

J Clin Med· May 2019

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A multicenter comparison of quantification methods for antisense oligonucleotide-induced DMD exon 51 skipping in Duchenne muscular dystrophy cell cultures.
Monika Hiller, Maria Sofia Falzarano, Iker Garcia-Jimenez, Valentina Sardone, Ruurd C Verheul

PLoS One· March 2019

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Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family.
Stefania Bigoni, Marcella Neri, Chiara Scotton, Roberto Farina, Patrizia Sabatelli, Maria Sofia Falzarano

Front Genet· January 2019

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Transcriptional and epigenetic analyses of the DMD locus reveal novel cis‑acting DNA elements that govern muscle dystrophin expression.
Samuele Gherardi, Matteo Bovolenta, Chiara Passarelli, Maria Sofia Falzarano, Paolo Pigini

Biochim Biophys Acta Gene Regul Mech· November 2017

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Antisense Oligonucleotide-Based Therapy for Neuromuscular Disease.
Valentina Sardone, Haiyan Zhou, Francesco Muntoni, Alessandra Ferlini, Maria Sofia Falzarano

Molecules· April 2017

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Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype.
Maria Sofia Falzarano, Domenico D'Amario, Andrea Siracusano, Massimo Massetti, Antonio Amodeo

Hum Gene Ther· October 2016

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