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Scientific Reports|June 16, 2018
Pathological modelling of pigmentation disorders associated with Hutchinson-Gilford Progeria Syndrome (HGPS) revealed an impaired melanogenesis pathway in iPS-derived melanocytesAlessandra Lo Cicero, Manoubia Saidani, Jennifer Allouche, et al.Lancet (London, England)|November 26, 2009
Human embryonic stem-cell derivatives for full reconstruction of the pluristratified epidermis: a preclinical studyHind Guenou, Xavier Nissan, Fernando Larcher, et al.International Journal of Molecular Sciences|April 13, 2023
Generating Functional and Highly Proliferative Melanocytes Derived from Human Pluripotent Stem Cells: A Promising Tool for Biotherapeutic Approaches to Treat Skin Pigmentation DisordersManoubia Saidani, Annabelle Darle, Margot Jarrige, et al.Proceedings of the National Academy of Sciences of the United States of America|July 8, 2015
In vitro modeling of hyperpigmentation associated to neurofibromatosis type 1 using melanocytes derived from human embryonic stem cellsJennifer Allouche, Nathalia Bellon, Manoubia Saidani, et al.Cells|January 30, 2021
The Future of Regenerative Medicine: Cell Therapy Using Pluripotent Stem Cells and Acellular Therapies Based on Extracellular VesiclesMargot Jarrige, Elie Frank, Elise Herardot, et al.Carcinogenesis|December 9, 2008
A novel Src kinase inhibitor reduces tumour formation in a skin carcinogenesis modelBryan Serrels, Alan Serrels, Susan M Mason, et al.Human Molecular Genetics|August 8, 2013
A defective Krab-domain zinc-finger transcription factor contributes to altered myogenesis in myotonic dystrophy type 1Morgane Gauthier, Antoine Marteyn, Jérôme Alexandre Denis, et al.Journal of Cell Science|February 28, 2013
mTOR-dependent proliferation defect in human ES-derived neural stem cells affected by myotonic dystrophy type 1Jérôme Alexandre Denis, Morgane Gauthier, Latif Rachdi, et al.The Journal of Investigative Dermatology|May 1, 2022
Human-Induced Pluripotent Stem Cell‒Derived Keratinocytes, a Useful Model to Identify and Explore the Pathological Phenotype of Epidermolysis Bullosa SimplexJulien Coutier, Manon Bonnette, Sabrina Martineau, et al.Pageof 2