Maria S. Falzarano

Ferrara, 44121, Italy

Last Updated: 09/26/2026

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Found 29 publications

Modulation of the JAK2-STAT3 pathway promotes expansion and maturation of human iPSC-derived myogenic progenitor cells.

Modulation of the JAK2-STAT3 pathway promotes expansion and maturation of human iPSC-derived myogenic progenitor cells.

Journal: Stem cell reports

Published: March 16, 2025

MECP2 mRNA Profile in Brain Tissues from a Rett Syndrome Patient and Three Human Controls: Mutated Allele Preferential Transcription and In Situ RNA Mapping.

MECP2 mRNA Profile in Brain Tissues from a Rett Syndrome Patient and Three Human Controls: Mutated Allele Preferential Transcription and In Situ RNA Mapping.

Journal: Biomolecules

Published: March 06, 2025

Modulation of the JAK2-STAT3 pathway promotes expansion and maturation of human iPSCs-derived myogenic progenitor cells.

Modulation of the JAK2-STAT3 pathway promotes expansion and maturation of human iPSCs-derived myogenic progenitor cells.

Journal: bioRxiv : the preprint server for biology

Published: December 23, 2024

mRNA in situ hybridization exhibits unbalanced nuclear/cytoplasmic dystrophin transcript repartition in Duchenne myogenic cells and skeletal muscle biopsies.

mRNA in situ hybridization exhibits unbalanced nuclear/cytoplasmic dystrophin transcript repartition in Duchenne myogenic cells and skeletal muscle biopsies.

Journal: Scientific reports

Published: May 04, 2023

Urine-Derived Stem Cells Express 571 Neuromuscular Disorders Causing Genes, Making Them a Potential in vitro Model for Rare Genetic Diseases.

Urine-Derived Stem Cells Express 571 Neuromuscular Disorders Causing Genes, Making Them a Potential in vitro Model for Rare Genetic Diseases.

Journal: Frontiers in physiology

Published: May 28, 2021

Circadian Genes as Exploratory Biomarkers in DMD: Results From Both the mdx Mouse Model and Patients.

Circadian Genes as Exploratory Biomarkers in DMD: Results From Both the mdx Mouse Model and Patients.

Journal: Frontiers in physiology

Published: March 10, 2021

RNA-seq in DMD urinary stem cells recognized muscle-related transcription signatures and addressed the identification of atypical mutations by whole-genome sequencing.

RNA-seq in DMD urinary stem cells recognized muscle-related transcription signatures and addressed the identification of atypical mutations by whole-genome sequencing.

Journal: HGG advances

Published: February 12, 2021

Innovative Therapeutic Approaches for Duchenne Muscular Dystrophy.

Innovative Therapeutic Approaches for Duchenne Muscular Dystrophy.

Journal: Journal of clinical medicine

Published: January 15, 2021

Dystrophin involvement in peripheral circadian SRF signalling.

Dystrophin involvement in peripheral circadian SRF signalling.

Journal: Life science alliance

Published: January 07, 2021

Corrigendum to: "Transcriptional and epigenetic analyses of the DMD locus reveal novel cis-acting DNA elements that govern muscle dystrophin expression". [Biochim. Biophys. Acta Gene Regul. Mech. 2017 Nov;1860(11):1138-1147.].

Corrigendum to: "Transcriptional and epigenetic analyses of the DMD locus reveal novel cis-acting DNA elements that govern muscle dystrophin expression". [Biochim. Biophys. Acta Gene Regul. Mech. 2017 Nov;1860(11):1138-1147.].

Journal: Biochimica et biophysica acta. Gene regulatory mechanisms

Published: November 04, 2020

Chitosan-Shelled Nanobubbles Irreversibly Encapsulate Morpholino Conjugate Antisense Oligonucleotides and Are Ineffective for Phosphorodiamidate Morpholino-Mediated Gene Silencing of DUX4.

Chitosan-Shelled Nanobubbles Irreversibly Encapsulate Morpholino Conjugate Antisense Oligonucleotides and Are Ineffective for Phosphorodiamidate Morpholino-Mediated Gene Silencing of DUX4.

Journal: Nucleic acid therapeutics

Published: July 18, 2020

The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study.

The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study.

Journal: Frontiers in genetics

Published: September 13, 2019

Showing 1-12 of 29

Last Updated: 09/26/2026