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Editorial: Skeletal Muscle Immunometabolism.
- Published in:
- 2021
- By:
- Publication type:
- Editorial
Nuclear poly(A)-binding protein aggregates misplace a pre-mRNA outside of SC35 speckle causing its abnormal splicing.
- Published in:
- Nucleic Acids Research, 2016, v. 44, n. 22, p. 10929, doi. 10.1093/nar/gkw703
- By:
- Publication type:
- Article
Poly(A) binding protein nuclear 1 levels affect alternative polyadenylation.
- Published in:
- Nucleic Acids Research, 2012, v. 40, n. 18, p. 9089, doi. 10.1093/nar/gks655
- By:
- Publication type:
- Article
Oxidative Stress in Disease and Aging: Mechanisms and Therapies 2016.
- Published in:
- Oxidative Medicine & Cellular Longevity, 2017, p. 1, doi. 10.1155/2017/4310469
- By:
- Publication type:
- Article
Les agrégats nucléaires dans la dystrophie musculaire oculopharyngée.
- Published in:
- Médecine Sciences, 2022, v. 38, p. 13, doi. 10.1051/medsci/2022175
- By:
- Publication type:
- Article
The Wnt/Ca<sup>2+</sup> pathway is involved in interneuronal communication mediated by tunneling nanotubes.
- Published in:
- EMBO Journal, 2019, v. 38, n. 23, p. N.PAG, doi. 10.15252/embj.2018101230
- By:
- Publication type:
- Article
Cell and molecular actors of fibrosis in muscle diseases.
- Published in:
- European Journal of Translational Myology, 2023, v. 33, n. 2, p. 35, doi. 10.4081/ejtm.2023.11427
- By:
- Publication type:
- Article
Deregulation of the ubiquitin-proteasome system is the predominant molecular pathology in OPMD animal models and patients.
- Published in:
- Skeletal Muscle, 2011, v. 1, n. 1, p. 2, doi. 10.1186/2044-5040-1-15
- By:
- Publication type:
- Article
Nuclear entrapment and extracellular depletion of PCOLCE is associated with muscle degeneration in oculopharyngeal muscular dystrophy.
- Published in:
- BMC Neurology, 2013, v. 13, n. 1, p. 1, doi. 10.1186/1471-2377-13-70
- By:
- Publication type:
- Article
Nuclear entrapment and extracellular depletion of PCOLCE is associated with muscle degeneration in oculopharyngeal muscular dystrophy.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Autologous Myoblast Transplantation for Oculopharyngeal Muscular Dystrophy: a Phase I/Iia Clinical Study.
- Published in:
- Molecular Therapy, 2014, v. 22, n. 1, p. 219, doi. 10.1038/mt.2013.155
- By:
- Publication type:
- Article
The Rag2<sup>-</sup>Il2rb<sup>-</sup>Dmd<sup>-</sup> Mouse: a Novel Dystrophic and Immunodeficient Model to Assess Innovating Therapeutic Strategies for Muscular Dystrophies.
- Published in:
- Molecular Therapy, 2013, v. 21, n. 10, p. 1950, doi. 10.1038/mt.2013.186
- By:
- Publication type:
- Article
Invited review: Stem cells and muscle diseases: advances in cell therapy strategies.
- Published in:
- Neuropathology & Applied Neurobiology, 2015, v. 41, n. 3, p. 270, doi. 10.1111/nan.12198
- By:
- Publication type:
- Article
How Can Proteomics Help to Elucidate the Pathophysiological Crosstalk in Muscular Dystrophy and Associated Multi-System Dysfunction?
- Published in:
- Proteomes, 2024, v. 12, n. 1, p. 4, doi. 10.3390/proteomes12010004
- By:
- Publication type:
- Article
Combined Therapies for Duchenne Muscular Dystrophy to Optimize Treatment Efficacy.
- Published in:
- Frontiers in Genetics, 2018, p. 1, doi. 10.3389/fgene.2018.00114
- By:
- Publication type:
- Article
Established PABPN1 intranuclear inclusions in OPMD muscle can be efficiently reversed by AAV-mediated knockdown and replacement of mutant expanded PABPN1.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 19, p. 3301, doi. 10.1093/hmg/ddz167
- By:
- Publication type:
- Article
Pharmacological modulation of the ER stress response ameliorates oculopharyngeal muscular dystrophy.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 10, p. 1694, doi. 10.1093/hmg/ddz007
- By:
- Publication type:
- Article
Positive in vivo heterologous gene regulation by electric pulses delivery with metallothionein I gene promoter.
- Published in:
- Journal of Gene Medicine, 2005, v. 7, n. 12, p. 1565, doi. 10.1002/jgm.811
- By:
- Publication type:
- Article
Combination of Myostatin Pathway Interference and Dystrophin Rescue Enhances Tetanic and Specific Force in Dystrophic mdx Mice.
- Published in:
- Molecular Therapy, 2010, v. 18, n. 5, p. 881, doi. 10.1038/mt.2009.322
- By:
- Publication type:
- Article
Design of Phosphorodiamidate Morpholino Oligomers (PMOs) for the Induction of Exon Skipping of the Human DMD Gene.
- Published in:
- Molecular Therapy, 2009, v. 17, n. 3, p. 554, doi. 10.1038/mt.2008.287
- By:
- Publication type:
- Article
Codon and mRNA Sequence Optimization of Microdystrophin Transgenes Improves Expression and Physiological Outcome in Dystrophic mdx Mice Following AAV2/8 Gene Transfer.
- Published in:
- Molecular Therapy, 2008, v. 16, n. 11, p. 1825, doi. 10.1038/mt.2008.186
- By:
- Publication type:
- Article
907. Development of Recombinant Novel Adeno-Associated Viral (rAAV) Vectors Encoding Optimised Microdystrophin cDNAs for Duchenne Muscular Dystrophy (DMD).
- Published in:
- Molecular Therapy, 2006, v. 13, p. S349, doi. 10.1016/j.ymthe.2006.08.997
- By:
- Publication type:
- Article
Mitochondrial Dysfunction Reveals the Role of mRNA Poly(A) Tail Regulation in Oculopharyngeal Muscular Dystrophy Pathogenesis.
- Published in:
- PLoS Genetics, 2015, v. 11, n. 3, p. 1, doi. 10.1371/journal.pgen.1005092
- By:
- Publication type:
- Article
A negative feedback loop between fibroadipogenic progenitors and muscle fibres involving endothelin promotes human muscle fibrosis.
- Published in:
- Journal of Cachexia, Sarcopenia & Muscle, 2022, v. 13, n. 3, p. 1771, doi. 10.1002/jcsm.12974
- By:
- Publication type:
- Article
Inhibition of myostatin improves muscle atrophy in oculopharyngeal muscular dystrophy (OPMD).
- Published in:
- Journal of Cachexia, Sarcopenia & Muscle, 2019, v. 10, n. 5, p. 1016, doi. 10.1002/jcsm.12438
- By:
- Publication type:
- Article
Molecular and phenotypic characterization of a mouse model of oculopharyngeal muscular dystrophy reveals severe muscular atrophy restricted to fast glycolytic fibres.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 11, p. 2191, doi. 10.1093/hmg/ddq098
- By:
- Publication type:
- Article
RNAi-mediated knockdown of dystrophin expression in adult mice does not lead to overt muscular dystrophy pathology.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 17, p. 2622, doi. 10.1093/hmg/ddn162
- By:
- Publication type:
- Article
Combined methods to evaluate human cells in muscle xenografts.
- Published in:
- PLoS ONE, 2019, v. 14, n. 5, p. 1, doi. 10.1371/journal.pone.0211522
- By:
- Publication type:
- Article
Transcriptomic analysis of dystrophin RNAi knockdown reveals a central role for dystrophin in muscle differentiation and contractileapparatus organization.
- Published in:
- BMC Genomics, 2010, v. 11, p. 345, doi. 10.1186/1471-2164-11-345
- By:
- Publication type:
- Article
Different outcomes of endurance and resistance exercise in skeletal muscles of Oculopharyngeal muscular dystrophy.
- Published in:
- Journal of Cachexia, Sarcopenia & Muscle, 2024, v. 15, n. 5, p. 1976, doi. 10.1002/jcsm.13546
- By:
- Publication type:
- Article