Impact of atopic dermatitis and loss-of-function mutations in the filaggrin gene on the development of occupational irritant contact dermatitis
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Title
Impact of atopic dermatitis and loss-of-function mutations in the filaggrin gene on the development of occupational irritant contact dermatitis
Authors
Keywords
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Journal
BRITISH JOURNAL OF DERMATOLOGY
Volume 168, Issue 2, Pages 326-332
Publisher
Wiley
Online
2012-10-06
DOI
10.1111/bjd.12083
References
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Related references
Note: Only part of the references are listed.- Filaggrin loss-of-function mutations are associated with enhanced expression of IL-1 cytokines in the stratum corneum of patients with atopic dermatitis and in a murine model of filaggrin deficiency
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- Altered stratum corneum barrier and enhanced percutaneous immune responses in filaggrin-null mice
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- Levels of filaggrin degradation products are influenced by both filaggrin genotype and atopic dermatitis severity
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- Filaggrin Genotype in Ichthyosis Vulgaris Predicts Abnormalities in Epidermal Structure and Function
- (2011) Robert Gruber et al. AMERICAN JOURNAL OF PATHOLOGY
- Combined occurrence of filaggrin mutations and IL-10 or IL-13 polymorphisms predisposes to atopic dermatitis
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- Intragenic Copy Number Variation within Filaggrin Contributes to the Risk of Atopic Dermatitis with a Dose-Dependent Effect
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- One Remarkable Molecule: Filaggrin
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- Filaggrin Mutations Associated with Skin and Allergic Diseases
- (2011) Alan D. Irvine et al. NEW ENGLAND JOURNAL OF MEDICINE
- The association between null mutations in the filaggrin gene and contact sensitization to nickel and other chemicals in the general population
- (2010) J.P. Thyssen et al. BRITISH JOURNAL OF DERMATOLOGY
- Filaggrin loss-of-function mutations are associated with early-onset eczema, eczema severity and transepidermal water loss at 3 months of age
- (2010) C. Flohr et al. BRITISH JOURNAL OF DERMATOLOGY
- The role of filaggrin in the atopic diathesis
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- Prediction of the incidence, recurrence, and persistence of atopic dermatitis in adolescence: A prospective cohort study
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- Skin Barrier Function in Healthy Subjects and Patients with Atopic Dermatitis in Relation to Filaggrin Loss-of-Function Mutations
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- Hardy-Weinberg Equilibrium Testing of Biological Ascertainment for Mendelian Randomization Studies
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- Filaggrin mutations may confer susceptibility to chronic hand eczema characterized by combined allergic and irritant contact dermatitis
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- Filaggrin deficiency confers a paracellular barrier abnormality that reduces inflammatory thresholds to irritants and haptens
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- Analysis of four prevalent filaggrin mutations (R501X, 2282del4, R2447X and S3247X) in Austrian and German patients with atopic dermatitis
- (2009) EK Greisenegger et al. JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY
- Loss-of-function polymorphisms in the filaggrin gene are associated with an increased susceptibility to chronic irritant contact dermatitis: a case-control study
- (2008) C.M. de Jongh et al. BRITISH JOURNAL OF DERMATOLOGY
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- Prevalent and Low-Frequency Null Mutations in the Filaggrin Gene Are Associated with Early-Onset and Persistent Atopic Eczema
- (2007) Sara J. Brown et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
- Loss-of-Function Mutations in the Filaggrin Gene and Allergic Contact Sensitization to Nickel
- (2007) Natalija Novak et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
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