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Journal of Proteome Research|June 11, 2010
New role for LEKTI in skin barrier formation: label-free quantitative proteomic identification of caspase 14 as a novel target for the protease inhibitor LEKTIKate Bennett, Robin Callard, Wendy Heywood, et al.
Journal of Cell Science|March 17, 2005
Connexin interaction patterns in keratinocytes revealed morphologically and by FRET analysisWei-Li Di, Yan Gu, John E A Common, et al.
The Journal of Investigative Dermatology|July 22, 2019
Human Mesenchymal Stromal Cells Engineered to Express Collagen VII Can Restore Anchoring Fibrils in Recessive Dystrophic Epidermolysis Bullosa Skin Graft ChimerasAnastasia Petrova, Christos Georgiadis, Roland A Fleck, et al.
Cell Communication & Adhesion|December 19, 2003
Cellular mechanisms of mutant connexins in skin disease and hearing lossJohn E A Common, Wei-Li Di, Derek Davies, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 30, 2010
Ex-vivo gene therapy restores LEKTI activity and corrects the architecture of Netherton syndrome-derived skin graftsWei-Li Di, Fernado Larcher, Ekaterina Semenova, et al.
Human Molecular Genetics|May 23, 2002
A mutation in GJB3 is associated with recessive erythrokeratodermia variabilis (EKV) and leads to defective trafficking of the connexin 31 proteinIrit Gottfried, Marina Landau, Fabian Glaser, et al.
The Journal of Allergy and Clinical Immunology|February 28, 2017
Persistent kallikrein 5 activation induces atopic dermatitis-like skin architecture independent of PAR2 activityYanan Zhu, Joanne Underwood, Derek Macmillan, et al.
Molecular Therapy. Methods & Clinical Development|July 9, 2020
Efficient CRISPR-Cas9-Mediated Gene Ablation in Human Keratinocytes to Recapitulate Genodermatoses: Modeling of Netherton SyndromeVictoria Gálvez, Esteban Chacón-Solano, Jose Bonafont, et al.
Human Molecular Genetics|August 8, 2002
Defective trafficking and cell death is characteristic of skin disease-associated connexin 31 mutationsWei-Li Di, James Monypenny, John E A Common, et al.
The Journal of Investigative Dermatology|November 10, 2019
Allele-Specific Small Interfering RNA Corrects Aberrant Cellular Phenotype in Keratitis-Ichthyosis-Deafness Syndrome KeratinocytesMing Yang Lee, Hong-Zhan Wang, Thomas W White, et al.
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