Filaggrin null mutations and association with contact allergy and allergic contact dermatitis: results from a tertiary dermatology clinic
Author:
Publisher
Wiley
Subject
Dermatology,Immunology and Allergy
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0536.2010.01748.x/fullpdf
Reference37 articles.
1. Filaggrin in the frontline: role in skin barrier function and disease;Sandilands;Journal of Cell Science,2009
2. Filaggrin in atopic dermatitis;O’Regan;Journal of Allergy and Clinical Immunology,2008
3. A homozygous frameshift mutation in the mouse Flg gene facilitates enhanced percutaneous allergen priming;Fallon;Nature Genetics,2009
4. Filaggrin-deficient mice exhibit TH17-dominated skin inflammation and permissiveness to epicutaneous sensitization with protein antigen;Oyoshi;Journal of Allergy and Clinical Immunology,2009
5. Filaggrin deficiency confers a paracellular barrier abnormality that reduces inflammatory thresholds to irritants and haptens;Scharschmidt;Journal of Allergy Clinical Immunology,2009
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