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Duchenne Muscular Dystrophy: From Diagnosis to Therapy

Molecules, 2015-10, Vol.20 (10), p.18168-18184

2015

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Antisense Oligonucleotide-Based Therapy for Neuromuscular Disease

Molecules (Basel, Switzerland), 2017-04, Vol.22 (4), p.563

2017

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Innovative Therapeutic Approaches for Duchenne Muscular Dystrophy

Journal of clinical medicine, 2021-02, Vol.10 (4), p.820

2021

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Urinary Stem Cells as Tools to Study Genetic Disease: Overview of the Literature

Journal of clinical medicine, 2019-05, Vol.8 (5), p.627

2019

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

Scientific reports, 2023-09, Vol.13 (1), p.15942-15942, Article 15942

2023

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

Frontiers in genetics, 2020-03, Vol.11, p.131-131

2020

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Nanodiagnostics and Nanodelivery Applications in Genetic Alterations

Current pharmaceutical design, 2018-01, Vol.24 (15), p.1717-1726

2018

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The DMD locus harbours multiple long non-coding RNAs which orchestrate and control transcription of muscle dystrophin mRNA isoforms

PloS one, 2012-09, Vol.7 (9), p.e45328-e45328

2012

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Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype

Human gene therapy, 2016-10, Vol.27 (10), p.772-783

2016

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A multicenter comparison of quantification methods for antisense oligonucleotide-induced DMD exon 51 skipping in Duchenne muscular dystrophy cell cultures

PloS one, 2018-10, Vol.13 (10), p.e0204485-e0204485

2018

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

Frontiers in physiology, 2021-10, Vol.12, p.716471-716471

2021

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

Frontiers in physiology, 2021-07, Vol.12, p.678974-678974

2021

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Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy

Journal of cell science, 2016-04, Vol.129 (8), p.1671-1684

2016

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Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family

Frontiers in genetics, 2019, Vol.9, p.723-723

2019

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Biodistribution and Molecular Studies on Orally Administered Nanoparticle-AON Complexes Encapsulated with Alginate Aiming at Inducing Dystrophin Rescue in mdx Mice

BioMed research international, 2013-01, Vol.2013 (2013), p.1-13

2013

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2-Phenyl-2,3-dihydro-1H-imidazo[1 ,2-b]pyrazole derivatives : New potent inhibitors of fMLP-induced neutrophil chemotaxis

Bioorganic & medicinal chemistry letters, 2007-07, Vol.17 (13), p.3696-3701

2007

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Signal transduction pathways triggered by selective formylpeptide analogues in human neutrophils

European journal of pharmacology, 2006-03, Vol.534 (1), p.1-11

2006

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Hydrophilic residues at position 3 highlight unforeseen features of the fMLP receptor pocket

European journal of pharmacology, 2003-05, Vol.469 (1), p.13-19

2003

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Nanoparticle delivery of antisense oligonucleotides and their application in the exon skipping strategy for Duchenne muscular dystrophy

Nucleic acid therapeutics, 2014-02, Vol.24 (1), p.87-100

2014

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Sodium Azide Induced Neuronal Damage In Vitro: Evidence for Non-Apoptotic Cell Death

Neurochemical research, 2009-05, Vol.34 (5), p.909-916

2009

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

Nucleic acid therapeutics, 2021-06, Vol.31 (3), p.201-207

2021

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Oligomeric formylpeptide activity on human neutrophils

European journal of medicinal chemistry, 2009-12, Vol.44 (12), p.4926-4930

2009

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Exon skipping-mediated dystrophin reading frame restoration for small mutations

Human mutation, 2009-11, Vol.30 (11), p.1527-1534

2009

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Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-terminal domain: a case report

BMC medical genetics, 2013-06, Vol.14 (1), p.59-59, Article 59

2013

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Duchenne Muscular Dystrophy: From Diagnosis to Therapy

Antisense Oligonucleotide-Based Therapy for Neuromuscular Disease

Innovative Therapeutic Approaches for Duchenne Muscular Dystrophy

Urinary Stem Cells as Tools to Study Genetic Disease: Overview of the Literature

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

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

Nanodiagnostics and Nanodelivery Applications in Genetic Alterations

The DMD locus harbours multiple long non-coding RNAs which orchestrate and control transcription of muscle dystrophin mRNA isoforms

Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype

A multicenter comparison of quantification methods for antisense oligonucleotide-induced DMD exon 51 skipping in Duchenne muscular dystrophy cell cultures

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

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

Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy

Tumor Necrosis Factor Receptor SF10A (TNFRSF10A) SNPs Correlate With Corticosteroid Response in Duchenne Muscular Dystrophy

Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family

Biodistribution and Molecular Studies on Orally Administered Nanoparticle-AON Complexes Encapsulated with Alginate Aiming at Inducing Dystrophin Rescue in mdx Mice

2-Phenyl-2,3-dihydro-1H-imidazo[1 ,2-b]pyrazole derivatives : New potent inhibitors of fMLP-induced neutrophil chemotaxis

Signal transduction pathways triggered by selective formylpeptide analogues in human neutrophils

Hydrophilic residues at position 3 highlight unforeseen features of the fMLP receptor pocket

Nanoparticle delivery of antisense oligonucleotides and their application in the exon skipping strategy for Duchenne muscular dystrophy

Sodium Azide Induced Neuronal Damage In Vitro: Evidence for Non-Apoptotic Cell Death

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

Oligomeric formylpeptide activity on human neutrophils

Exon skipping-mediated dystrophin reading frame restoration for small mutations

Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-terminal domain: a case report

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