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American Journal of Human Genetics|August 26, 2014
Mutations in GRHL2 result in an autosomal-recessive ectodermal Dysplasia syndromeGabriela Petrof, Arti Nanda, Jake Howden, et al.
Eclinicalmedicine|November 3, 2025
Mesenchymal stromal cell infusions of umbilical cord-derived mesenchymal stromal cells in children with recessive dystrophic epidermolysis bullosa (MissionEB): a randomised, double-blind, placebo controlled, crossover, phase 3 trial with an internal phase 1 dose de-escalation phaseMaria L Bageta, Pablo Lopez-Balboa, Matt Bursnall, et al.
The Journal of Investigative Dermatology|July 24, 2015
Activating CARD14 Mutations Are Associated with Generalized Pustular Psoriasis but Rarely Account for Familial Recurrence in Psoriasis VulgarisDorottya M Berki, Lu Liu, Siew-Eng Choon, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 2, 2024
Lentiviral expression of wild-type LAMA3A restores cell adhesion in airway basal cells from children with epidermolysis bullosaChun Hang Lau, Maral J Rouhani, Elizabeth F Maughan, et al.
The British Journal of Dermatology|September 5, 2024
An expert consensus on managing dupilumab-related ocular surface disorders in people with atopic dermatitis 2024Michael R Ardern-Jones, Sara J Brown, Carsten Flohr, et al.
The Journal of Investigative Dermatology|April 3, 2014
Epithelial inflammation resulting from an inherited loss-of-function mutation in EGFRPatrick Campbell, Penny E Morton, Takuya Takeichi, et al.
JCI Insight|October 19, 2021
Clinical trial of ABCB5+ mesenchymal stem cells for recessive dystrophic epidermolysis bullosaDimitra Kiritsi, Kathrin Dieter, Elke Niebergall-Roth, et al.
Journal of the American Academy of Dermatology|December 2, 2019
Phase I/II open-label trial of intravenous allogeneic mesenchymal stromal cell therapy in adults with recessive dystrophic epidermolysis bullosaEllie Rashidghamat, Tendai Kadiyirire, Salma Ayis, et al.
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