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Current Opinion in Pharmacology
|
December 25, 2022
Update on anti-fibrotic pharmacotherapies in skeletal muscle disease
Laura Muraine, Mona Bensalah, Gillian Butler-Browne, et al.
Elife
|
August 15, 2018
The role of Pitx2 and Pitx3 in muscle stem cells gives new insights into P38α MAP kinase and redox regulation of muscle regeneration
Aurore L'honoré, Pierre-Henri Commère, Elisa Negroni, et al.
Frontiers in Cell and Developmental Biology
|
October 6, 2022
Muscle fibro-adipogenic progenitors from a single-cell perspective: Focus on their "virtual" secretome
Elisa Negroni, Maria Kondili, Laura Muraine, et al.
Stem Cell Research
|
April 1, 2014
Glycosaminoglycan mimetic improves enrichment and cell functions of human endothelial progenitor cell colonies
Fabien Chevalier, Mélanie Lavergne, Elisa Negroni, et al.
Journal of Neuropathology and Experimental Neurology
|
July 9, 2014
Glycosaminoglycan modifications in Duchenne muscular dystrophy: specific remodeling of chondroitin sulfate/dermatan sulfate
Elisa Negroni, Emilie Henault, Fabien Chevalier, et al.
Journal of Neuropathology and Experimental Neurology
|
February 13, 2013
Atrophy, fibrosis, and increased PAX7-positive cells in pharyngeal muscles of oculopharyngeal muscular dystrophy patients
Teresa Gidaro, Elisa Negroni, Sophie Perié, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 23, 2009
In vivo myogenic potential of human CD133+ muscle-derived stem cells: a quantitative study
Elisa Negroni, Ingo Riederer, Soraya Chaouch, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 29, 2017
Obestatin Increases the Regenerative Capacity of Human Myoblasts Transplanted Intramuscularly in an Immunodeficient Mouse Model
Icia Santos-Zas, Elisa Negroni, Kamel Mamchaoui, et al.
Human Gene Therapy
|
April 11, 2009
Immortalized skin fibroblasts expressing conditional MyoD as a renewable and reliable source of converted human muscle cells to assess therapeutic strategies for muscular dystrophies: validation of an exon-skipping approach to restore dystrophin in Duchenne muscular dystrophy cells
Soraya Chaouch, Vincent Mouly, Aurélie Goyenvalle, et al.
Plos One
|
May 4, 2019
Combined methods to evaluate human cells in muscle xenografts
Mona Bensalah, Pierre Klein, Ingo Riederer, et al.
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Search research articles
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Showing results (11-20 of 46) with videos related to
Sort By:
Page
of 5
Current Opinion in Pharmacology
|
December 25, 2022
Update on anti-fibrotic pharmacotherapies in skeletal muscle disease
Laura Muraine, Mona Bensalah, Gillian Butler-Browne, et al.
Elife
|
August 15, 2018
The role of Pitx2 and Pitx3 in muscle stem cells gives new insights into P38α MAP kinase and redox regulation of muscle regeneration
Aurore L'honoré, Pierre-Henri Commère, Elisa Negroni, et al.
Frontiers in Cell and Developmental Biology
|
October 6, 2022
Muscle fibro-adipogenic progenitors from a single-cell perspective: Focus on their "virtual" secretome
Elisa Negroni, Maria Kondili, Laura Muraine, et al.
Stem Cell Research
|
April 1, 2014
Glycosaminoglycan mimetic improves enrichment and cell functions of human endothelial progenitor cell colonies
Fabien Chevalier, Mélanie Lavergne, Elisa Negroni, et al.
Journal of Neuropathology and Experimental Neurology
|
July 9, 2014
Glycosaminoglycan modifications in Duchenne muscular dystrophy: specific remodeling of chondroitin sulfate/dermatan sulfate
Elisa Negroni, Emilie Henault, Fabien Chevalier, et al.
Journal of Neuropathology and Experimental Neurology
|
February 13, 2013
Atrophy, fibrosis, and increased PAX7-positive cells in pharyngeal muscles of oculopharyngeal muscular dystrophy patients
Teresa Gidaro, Elisa Negroni, Sophie Perié, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 23, 2009
In vivo myogenic potential of human CD133+ muscle-derived stem cells: a quantitative study
Elisa Negroni, Ingo Riederer, Soraya Chaouch, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 29, 2017
Obestatin Increases the Regenerative Capacity of Human Myoblasts Transplanted Intramuscularly in an Immunodeficient Mouse Model
Icia Santos-Zas, Elisa Negroni, Kamel Mamchaoui, et al.
Human Gene Therapy
|
April 11, 2009
Immortalized skin fibroblasts expressing conditional MyoD as a renewable and reliable source of converted human muscle cells to assess therapeutic strategies for muscular dystrophies: validation of an exon-skipping approach to restore dystrophin in Duchenne muscular dystrophy cells
Soraya Chaouch, Vincent Mouly, Aurélie Goyenvalle, et al.
Plos One
|
May 4, 2019
Combined methods to evaluate human cells in muscle xenografts
Mona Bensalah, Pierre Klein, Ingo Riederer, et al.
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of 5