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Stephanie Duguez

Showing results (21-30 of 34) with videos related to

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Skeletal Muscle|July 10, 2020
Optimized method for extraction of exosomes from human primary muscle cellsLaura Le Gall, Zamalou Gisele Ouandaogo, Ekene Anakor, et al.
Molecular Therapy. Nucleic Acids|June 19, 2017
Correction of the Exon 2 Duplication in DMD Myoblasts by a Single CRISPR/Cas9 SystemAnnalisa Lattanzi, Stephanie Duguez, Arianna Moiani, et al.
Skeletal Muscle|May 20, 2015
Muscular dystrophy in the mdx mouse is a severe myopathy compounded by hypotrophy, hypertrophy and hyperplasiaWilliam Duddy, Stephanie Duguez, Helen Johnston, et al.
Human Molecular Genetics|April 25, 2014
Survival motor neuron protein deficiency impairs myotube formation by altering myogenic gene expression and focal adhesion dynamicsKatherine V Bricceno, Tara Martinez, Evgenia Leikina, et al.
Cellular and Molecular Life Sciences : CMLS|January 25, 2013
Dystrophin deficiency leads to disturbance of LAMP1-vesicle-associated protein secretionStephanie Duguez, William Duddy, Helen Johnston, et al.
Expert Review of Proteomics|July 20, 2012
Advances in the proteomic investigation of the cell secretomeKristy J Brown, Catherine A Formolo, Haeri Seol, et al.
The Journal of Infectious Diseases|April 20, 2019
Necrotizing Soft Tissue Infection Staphylococcus aureus but not S. pyogenes Isolates Display High Rates of Internalization and Cytotoxicity Toward Human MyoblastsJessica Baude, Sylvère Bastien, Yves Gillet, et al.
Biogerontology|May 14, 2013
Age-dependent alteration in muscle regeneration: the critical role of tissue nicheLaura Barberi, Bianca Maria Scicchitano, Manuela De Rossi, et al.
Scientific Reports|November 17, 2025
Mifepristone alone and in combination with scAAV9-SMN1 gene therapy improves disease phenotypes in Smn<sup>2B/-</sup> spinal muscular atrophy miceEmma R Sutton, Eve McCallion, Joseph M Hoolachan, et al.
Annals of Neurology|May 29, 2015
Correlation between low FAT1 expression and early affected muscle in facioscapulohumeral muscular dystrophyVirginie Mariot, Stephane Roche, Christophe Hourdé, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Skeletal Muscle|July 10, 2020
Optimized method for extraction of exosomes from human primary muscle cellsLaura Le Gall, Zamalou Gisele Ouandaogo, Ekene Anakor, et al.
Molecular Therapy. Nucleic Acids|June 19, 2017
Correction of the Exon 2 Duplication in DMD Myoblasts by a Single CRISPR/Cas9 SystemAnnalisa Lattanzi, Stephanie Duguez, Arianna Moiani, et al.
Skeletal Muscle|May 20, 2015
Muscular dystrophy in the mdx mouse is a severe myopathy compounded by hypotrophy, hypertrophy and hyperplasiaWilliam Duddy, Stephanie Duguez, Helen Johnston, et al.
Human Molecular Genetics|April 25, 2014
Survival motor neuron protein deficiency impairs myotube formation by altering myogenic gene expression and focal adhesion dynamicsKatherine V Bricceno, Tara Martinez, Evgenia Leikina, et al.
Cellular and Molecular Life Sciences : CMLS|January 25, 2013
Dystrophin deficiency leads to disturbance of LAMP1-vesicle-associated protein secretionStephanie Duguez, William Duddy, Helen Johnston, et al.
Expert Review of Proteomics|July 20, 2012
Advances in the proteomic investigation of the cell secretomeKristy J Brown, Catherine A Formolo, Haeri Seol, et al.
The Journal of Infectious Diseases|April 20, 2019
Necrotizing Soft Tissue Infection Staphylococcus aureus but not S. pyogenes Isolates Display High Rates of Internalization and Cytotoxicity Toward Human MyoblastsJessica Baude, Sylvère Bastien, Yves Gillet, et al.
Biogerontology|May 14, 2013
Age-dependent alteration in muscle regeneration: the critical role of tissue nicheLaura Barberi, Bianca Maria Scicchitano, Manuela De Rossi, et al.
Scientific Reports|November 17, 2025
Mifepristone alone and in combination with scAAV9-SMN1 gene therapy improves disease phenotypes in Smn<sup>2B/-</sup> spinal muscular atrophy miceEmma R Sutton, Eve McCallion, Joseph M Hoolachan, et al.
Annals of Neurology|May 29, 2015
Correlation between low FAT1 expression and early affected muscle in facioscapulohumeral muscular dystrophyVirginie Mariot, Stephane Roche, Christophe Hourdé, et al.
Pageof 4