Mutations in the filaggrin gene in Han Chinese patients with atopic dermatitis
Author:
Publisher
Wiley
Subject
Immunology,Immunology and Allergy
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1398-9995.2010.02493.x/fullpdf
Reference31 articles.
1. How epidemiology has challenged 3 prevailing concepts about atopic dermatitis;Williams;J Allergy Clin Immunol,2006
2. Proceedings of the 4th Georg Rajka International Symposium on Atopic Dermatitis, Arcachon, France, September 15-17, 2005;Taïeb;J Allergy Clin Immunol,2006
3. New perspectives on epidermal barrier dysfunction in atopic dermatitis: gene-environment interactions;Cork;J Allergy Clin Immunol,2006
4. Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris;Smith;Nat Genet,2006
5. Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis;Palmer;Nat Genet,2006
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1. Genetic analysis of seven patients with inherited ichthyosis and Nagashima‑type palmoplantar keratoderma;Molecular Medicine Reports;2024-05-01
2. Filaggrin loss-of-function variants are associated with atopic dermatitis phenotypes in a diverse, early-life prospective cohort;JCI Insight;2024-04-02
3. Filaggrin and beyond;Annals of Allergy, Asthma & Immunology;2024-02
4. Candidate Gene Association Studies in Atopic Dermatitis in Participants of European and Asian Ancestry: A Systematic Review and Meta-Analysis;Genes;2023-07-17
5. Filaggrin gene polymorphisms in Indian children with atopic dermatitis: A cross-sectional multicentre study;Indian Journal of Dermatology, Venereology and Leprology;2023-04-01
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