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Orphanet Journal of Rare Diseases|July 19, 2022
RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell-cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual developmentElena Dellambra, Sonia Cordisco, Francesca Delle Monache, et al.The Journal of Investigative Dermatology|March 1, 2014
Nectin-4 mutations causing ectodermal dysplasia with syndactyly perturb the rac1 pathway and the kinetics of adherens junction formationPaola Fortugno, Emmanuelle Josselin, Konstantinos Tsiakas, et al.Human Molecular Genetics|March 17, 2018
Defective kinesin binding of TUBB2A causes progressive spastic ataxia syndrome resembling sacsinopathyAntonella Sferra, Fabiana Fattori, Teresa Rizza, et al.The EMBO Journal|September 8, 2006
New functions of XPC in the protection of human skin cells from oxidative damageMariarosaria D'Errico, Eleonora Parlanti, Massimo Teson, et al.Human Molecular Genetics|February 27, 2022
RIPK4 regulates cell-cell adhesion in epidermal development and homeostasisPaola Fortugno, Rosanna Monetta, Manuel Belli, et al.Journal of Biomedical Science|February 13, 2025
miR-200c inhibition and catalase accelerate diabetic wound healingMarco D'Agostino, Sara Sileno, Daniela Lulli, et al.Journal of Biomedical Science|February 26, 2026
TRKB-based signature identifies high-risk squamous cell carcinoma cases and TRKB blockade reprograms tumor and stromal cells toward suppressive phenotypesValeria Bartolocci, Alessio Capone, Rosanna Monetta, et al.The British Journal of Dermatology|May 31, 2024
Histone deacetylase inhibition mitigates fibrosis-driven disease progression in recessive dystrophic epidermolysis bullosaAlessia Primerano, Emanuela De Domenico, Francesca Cianfarani, et al.Pageof 2