miR‐31 modulates dystrophin expression: new implications for Duchenne muscular dystrophy therapy-Reference-Cited by-同舟云学术

miR‐31 modulates dystrophin expression: new implications for Duchenne muscular dystrophy therapy

Published:2011-01-07 Issue:2 Volume:12 Page:136-141
ISSN:1469-221X
Container-title:EMBO reports
language:en
Short-container-title:EMBO Rep

Author:

Cacchiarelli Davide¹,Incitti Tania¹,Martone Julie¹,Cesana Marcella¹,Cazzella Valentina¹,Santini Tiziana¹,Sthandier Olga¹,Bozzoni Irene¹

Affiliation:

1. Department of Biology and Biotechnology ‘C. Darwin’, Institut Pasteur Cenci‐Bolognetti and IBPM—Sapienza, University of Rome Piazzele Aldo Moro 5 Rome 00185 Italy

Publisher

EMBO

Subject

Genetics,Molecular Biology,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1038/embor.2010.208

Reference24 articles.

1. Therapeutic antisense-induced exon skipping in cultured muscle cells from six different DMD patients

2. Systemic delivery of morpholino oligonucleotide restores dystrophin expression bodywide and improves dystrophic pathology

3. Targeted Exon Skipping in Transgenic hDMD Mice: A Model for Direct Preclinical Screening of Human-Specific Antisense Oligonucleotides

4. MicroRNAs Involved in Molecular Circuitries Relevant for the Duchenne Muscular Dystrophy Pathogenesis Are Controlled by the Dystrophin/nNOS Pathway

5. The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation

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