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Cells|January 11, 2019
Bring It to an End: Does Telomeres Size Matter?Camille Laberthonnière, Frédérique Magdinier, Jérôme D Robin
Cells|July 14, 2023
Single-Cell RNA Sequencing: Opportunities and Challenges for Studies on Corneal Biology in Health and DiseaseJulian A Arts, Camille Laberthonnière, Dulce Lima Cunha, et al.
Scientific Reports|July 19, 2019
Analysis of the 4q35 chromatin organization reveals distinct long-range interactions in patients affected with Facio-Scapulo-Humeral DystrophyMarie-Cécile Gaillard, Natacha Broucqsault, Julia Morere, et al.
Neurology. Genetics|December 25, 2019
Methylation hotspots evidenced by deep sequencing in patients with facioscapulohumeral dystrophy and mosaicismStéphane Roche, Camille Dion, Natacha Broucqsault, et al.
International Journal of Molecular Sciences|November 26, 2022
Generation of the First Human In Vitro Model for McArdle Disease Based on iPSC TechnologyMaría Del Carmen Ortuño-Costela, Victoria Cerrada, Ana Moreno-Izquierdo, et al.
Journal of Cachexia, Sarcopenia and Muscle|December 3, 2021
Facioscapulohumeral dystrophy weakened sarcomeric contractility is mimicked in induced pluripotent stem cells-derived innervated muscle fibresCamille Laberthonnière, Elva-Maria Novoa-Del-Toro, Mégane Delourme, et al.
Nucleic Acids Research|June 19, 2023
In skeletal muscle and neural crest cells, SMCHD1 regulates biological pathways relevant for Bosma syndrome and facioscapulohumeral dystrophy phenotypeCamille Laberthonnière, Mégane Delourme, Raphaël Chevalier, et al.
Plos Biology|October 19, 2023
Identification of the regulatory circuit governing corneal epithelial fate determination and diseaseJos G A Smits, Dulce Lima Cunha, Maryam Amini, et al.
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