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Article

Evidence That Loss-of-Function Filaggrin Gene Mutations Evolved in Northern Europeans to Favor Intracutaneous Vitamin D3 Production

14 May 2014

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 25506102
DOI: 10.1007/s11692-014-9282-7

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Related research

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Evidence That Loss-of-Function Filaggrin Gene Mutations Evolved in Northern Europeans to Favor Intracutaneous Vitamin D3 ProductionPMID 25506102Read ↗

It Remains Unknown Whether Filaggrin Gene Mutations Evolved to Increase Cutaneous Synthesis of Vitamin D.Semantic proximity Read ↗

Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitisSemantic proximity Read ↗

Two Common Loss-of-Function Mutations within the Filaggrin Gene Predispose for Early Onset of Atopic DermatitisSemantic proximity Read ↗

[Filaggrin gene mutations are frequent and increase the risk of skin disease].Semantic proximity Read ↗

Common filaggrin gene loss-of-function variants are associated with skin cancer risk.Semantic proximity Read ↗

Filaggrin haploinsufficiency among patients with dermatitis from a tertiary referral centre: early findings and possible phenotype.Semantic proximity Read ↗

Filaggrin mutations associated with skin and allergic diseases.Semantic proximity Read ↗

The filaggrin story: novel insights into skin-barrier function and diseaseSemantic proximity Read ↗

Filaggrin mutations and the skin.Semantic proximity Read ↗

Filaggrin loss-of-function mutations and association with allergic diseases.Semantic proximity Read ↗

The clinical relevance of filaggrin mutations: Effect on allergic disease.Semantic proximity Read ↗

De Novo Occurrence of the Filaggrin Mutation p.R501X with Prevalent Mutation c.3321delA in a Japanese Family with Ichthyosis Vulgaris Complicated by Atopic DermatitisSemantic proximity Read ↗

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