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Kallikrein 5 induces atopic dermatitis–like lesions through PAR2-mediated thymic stromal lymphopoietin expression in Netherton syndrome
Netherton syndrome (NS) is a severe genetic skin disease with constant atopic manifestations that is caused by mutations in the serine protease inhibitor Kazal-type 5 (SPINK5) gene, which encodes the protease inhibitor lymphoepithelial Kazal-type–related inhibitor (LEKTI). Lack of LEKTI causes strat...
Autores principales: | Briot, Anaïs, Deraison, Céline, Lacroix, Matthieu, Bonnart, Chrystelle, Robin, Aurélie, Besson, Céline, Dubus, Pierre, Hovnanian, Alain |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2715042/ https://www.ncbi.nlm.nih.gov/pubmed/19414552 http://dx.doi.org/10.1084/jem.20082242 |
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