Null Mutations in the Filaggrin Gene (FLG) Determine Major Susceptibility to Early-Onset Atopic Dermatitis that Persists into Adulthood
Open Access
- 1 March 2007
- journal article
- Published by Elsevier BV in Journal of Investigative Dermatology
- Vol. 127 (3), 564-567
- https://doi.org/10.1038/sj.jid.5700587
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Prevalent and Rare Mutations in the Gene Encoding Filaggrin Cause Ichthyosis Vulgaris and Predispose Individuals to Atopic DermatitisJournal of Investigative Dermatology, 2006
- Skin barrier function and allergic riskNature Genetics, 2006
- Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitisNature Genetics, 2006
- Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgarisNature Genetics, 2006
- The cornified envelope: a model of cell death in the skinNature Reviews Molecular Cell Biology, 2005
- Adult-onset atopic dermatitisJournal of the American Academy of Dermatology, 2005
- Factors influencing atopic dermatitis-a questionnaire survey of schoolchildren's perceptionsBritish Journal of Dermatology, 2004
- The U.K. Working Party's Diagnostic Criteria for Atopic Dermatitis..British Journal of Dermatology, 1994
- The prevalence of childhood atopic eczema in a general populationJournal of the American Academy of Dermatology, 1994
- Organization, structure, and polymorphisms of the human profilaggrin geneBiochemistry, 1990