Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Dermatologic Clinics|May 8, 2010
Gene therapy for recessive dystrophic epidermolysis bullosaMatthias Titeux, Valérie Pendaries, Alain Hovnanian
Oncogene|November 7, 2003
Retinoic acid receptors interfere with the TGF-beta/Smad signaling pathway in a ligand-specific mannerValérie Pendaries, Franck Verrecchia, Serge Michel, et al.
Human Mutation|November 22, 2007
A frequent functional SNP in the MMP1 promoter is associated with higher disease severity in recessive dystrophic epidermolysis bullosaMatthias Titeux, Valérie Pendaries, Laure Tonasso, et al.
Oncogene|February 3, 2005
The steroid receptor co-activator-1 (SRC-1) potentiates TGF-beta/Smad signaling: role of p300/CBPSylviane Dennler, Valérie Pendaries, Charlotte Tacheau, et al.
Journal of Dermatological Science|March 1, 2017
Lowering relative humidity level increases epidermal protein deimination and drives human filaggrin breakdownLaura Cau, Valérie Pendaries, Emeline Lhuillier, et al.
Journal of Dermatological Science|April 26, 2018
Stabilization of microtubules restores barrier function after cytokine-induced defects in reconstructed human epidermisChiung-Yueh Hsu, Nicolas Lecland, Valérie Pendaries, et al.
The Journal of Biological Chemistry|December 3, 2015
Hyaluronan Does Not Regulate Human Epidermal Keratinocyte Proliferation and DifferentiationJérémy Malaisse, Valérie Pendaries, Fanny Hontoir, et al.
Biological Chemistry|May 29, 2015
Defects of corneocyte structural proteins and epidermal barrier in atopic dermatitisMarina Le Lamer, Laurence Pellerin, Marie Reynier, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|September 11, 2018
Refined Immunochemical Characterization in Healthy Dog Skin of the Epidermal Cornification Proteins, Filaggrin, and CorneodesmosinDidier Pin, Valérie Pendaries, Sokhna Keita Alassane, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 21, 2010
SIN retroviral vectors expressing COL7A1 under human promoters for ex vivo gene therapy of recessive dystrophic epidermolysis bullosaMatthias Titeux, Valérie Pendaries, Maria A Zanta-Boussif, et al.
Pageof 2