Search details
1.
Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy.
J Cell Sci
; 129(8): 1671-84, 2016 Apr 15.
Article
in English
| MEDLINE | ID: mdl-26945058
2.
Antisense Oligonucleotide-Based Therapy for Neuromuscular Disease.
Molecules
; 22(4)2017 Apr 05.
Article
in English
| MEDLINE | ID: mdl-28379182
3.
Duchenne Muscular Dystrophy: From Diagnosis to Therapy.
Molecules
; 20(10): 18168-84, 2015 Oct 07.
Article
in English
| MEDLINE | ID: mdl-26457695
4.
mRNA in situ hybridization exhibits unbalanced nuclear/cytoplasmic dystrophin transcript repartition in Duchenne myogenic cells and skeletal muscle biopsies.
Sci Rep
; 13(1): 15942, 2023 09 24.
Article
in English
| MEDLINE | ID: mdl-37743371
5.
Rapid, comprehensive analysis of the dystrophin transcript by a custom micro-fluidic exome array.
Hum Mutat
; 33(3): 572-81, 2012 Mar.
Article
in English
| MEDLINE | ID: mdl-22223181
6.
Innovative Therapeutic Approaches for Duchenne Muscular Dystrophy.
J Clin Med
; 10(4)2021 Feb 17.
Article
in English
| MEDLINE | ID: mdl-33671409
7.
Chitosan-Shelled Nanobubbles Irreversibly Encapsulate Morpholino Conjugate Antisense Oligonucleotides and Are Ineffective for Phosphorodiamidate Morpholino-Mediated Gene Silencing of DUX4.
Nucleic Acid Ther
; 31(3): 201-207, 2021 06.
Article
in English
| MEDLINE | ID: mdl-32679000
8.
Urine-Derived Stem Cells Express 571 Neuromuscular Disorders Causing Genes, Making Them a Potential in vitro Model for Rare Genetic Diseases.
Front Physiol
; 12: 716471, 2021.
Article
in English
| MEDLINE | ID: mdl-34744760
9.
Circadian Genes as Exploratory Biomarkers in DMD: Results From Both the mdx Mouse Model and Patients.
Front Physiol
; 12: 678974, 2021.
Article
in English
| MEDLINE | ID: mdl-34305639
10.
Dystrophin involvement in peripheral circadian SRF signalling.
Life Sci Alliance
; 4(10)2021 10.
Article
in English
| MEDLINE | ID: mdl-34389686
11.
Tumor Necrosis Factor Receptor SF10A (TNFRSF10A) SNPs Correlate With Corticosteroid Response in Duchenne Muscular Dystrophy.
Front Genet
; 11: 605, 2020.
Article
in English
| MEDLINE | ID: mdl-32719714
12.
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study.
Front Genet
; 11: 131, 2020.
Article
in English
| MEDLINE | ID: mdl-32194622
13.
1-Methyl and 1-(2-hydroxyalkyl)-5-(3-alkyl/cycloalkyl/phenyl/naphthylureido)-1H-pyrazole-4-carboxylic acid ethyl esters as potent human neutrophil chemotaxis inhibitors.
Bioorg Med Chem
; 17(9): 3379-87, 2009 May 01.
Article
in English
| MEDLINE | ID: mdl-19362486
14.
Urinary Stem Cells as Tools to Study Genetic Disease: Overview of the Literature.
J Clin Med
; 8(5)2019 May 08.
Article
in English
| MEDLINE | ID: mdl-31071994
15.
Nanodiagnostics and Nanodelivery Applications in Genetic Alterations.
Curr Pharm Des
; 24(15): 1717-1726, 2018.
Article
in English
| MEDLINE | ID: mdl-29318963
16.
A multicenter comparison of quantification methods for antisense oligonucleotide-induced DMD exon 51 skipping in Duchenne muscular dystrophy cell cultures.
PLoS One
; 13(10): e0204485, 2018.
Article
in English
| MEDLINE | ID: mdl-30278058
17.
Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family.
Front Genet
; 9: 723, 2018.
Article
in English
| MEDLINE | ID: mdl-30740127
18.
Transcriptional and epigenetic analyses of the DMD locus reveal novel cisacting DNA elements that govern muscle dystrophin expression.
Biochim Biophys Acta Gene Regul Mech
; 1860(11): 1138-1147, 2017 Nov.
Article
in English
| MEDLINE | ID: mdl-28867298
19.
Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype.
Hum Gene Ther
; 27(10): 772-783, 2016 10.
Article
in English
| MEDLINE | ID: mdl-27530229
20.
Nanoparticle delivery of antisense oligonucleotides and their application in the exon skipping strategy for Duchenne muscular dystrophy.
Nucleic Acid Ther
; 24(1): 87-100, 2014 Feb.
Article
in English
| MEDLINE | ID: mdl-24506782