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Article

Full Sequencing of the FLG Gene in Italian Patients with Atopic Eczema: Evidence of New Mutations, but Lack of an Association

3 Feb 2011

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Share to Allergic Rhinitis and Sensitization
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Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 21289640
DOI: 10.1038/jid.2010.398

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 10 closest

Full Sequencing of the FLG Gene in Italian Patients with Atopic Eczema: Evidence of New Mutations, but Lack of an AssociationPMID 21289640Read ↗

Prevalence of FLG loss‐of‐function mutations R501X, 2282del4, and R2447X in Spanish children with atopic dermatitisSemantic proximity Read ↗

Filaggrin loss-of-function mutations as a predictor for atopic eczema, allergic sensitization and eczema-associated asthma in Polish children population.Semantic proximity Read ↗

Influence of FLG mutations and TSLP polymorphisms on atopic dermatitis onset age.Semantic proximity Read ↗

Association of FLG single nucleotide variations with clinical phenotypes of atopic dermatitis.Semantic proximity Read ↗

The Value of FLG Null Mutations in Predicting Treatment Response in Atopic Dermatitis: An Observational Study in Finnish Patients.Semantic proximity Read ↗

Lack of association between Toll-like receptor 2 and Toll-like receptor 4 polymorphisms and atopic eczemaSemantic proximity Read ↗

FLG single nucleotide polymorphisms in chronic idiopathic urticaria.Semantic proximity Read ↗

GLCCI1 rs37973 does not influence treatment response to inhaled corticosteroids in white subjects with asthmaSemantic proximity Read ↗

Filaggrin null alleles are not associated with psoriasis.Semantic proximity Read ↗

A comprehensive analysis of the COL29A1 gene does not support a role in eczema.Semantic proximity Read ↗

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