Heterozygous Null Alleles in Filaggrin Contribute to Clinical Dry Skin in Young Adults and the Elderly (Q57638950)

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25 December 2019

title

Heterozygous null alleles in filaggrin contribute to clinical dry skin in young adults and the elderly (English)

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25 December 2019

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3

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Colin Palmer

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Irwin McLean

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author name string

Ann Sergeant

1

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Martin Porter

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Linda E Campbell

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Frances J D Smith

6

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Colin S Munro

8

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language of work or name

English

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publication date

6 November 2008

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Journal of Investigative Dermatology

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published in

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volume

129

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issue

4

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page(s)

1042-1045

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https://scigraph.springernature.com/pub.10.1038/jid.2008.324

25 December 2019

exact match

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cites work

Toward a major risk factor for atopic eczema: meta-analysis of filaggrin polymorphism data

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.324

7 January 2021

Filaggrin null mutations and childhood atopic eczema: A population-based case-control study

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.324

7 January 2021

Prevalent and Low-Frequency Null Mutations in the Filaggrin Gene Are Associated with Early-Onset and Persistent Atopic Eczema

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.324

7 January 2021

Filaggrin repeat number polymorphism is associated with a dry skin phenotype

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.324

7 January 2021

The burden of disease associated with filaggrin mutations: a population-based, longitudinal birth cohort study

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.324

7 January 2021

Loss-of-Function Mutations in the Filaggrin Gene Lead to Reduced Level of Natural Moisturizing Factor in the Stratum Corneum

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.324

7 January 2021

Loss-of-function mutations in the filaggrin gene and allergic contact sensitization to nickel

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.324

7 January 2021

Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.324

7 January 2021

Stratum corneum lipids: the effect of ageing and the seasons

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.324

7 January 2021

Prevalent and Rare Mutations in the Gene Encoding Filaggrin Cause Ichthyosis Vulgaris and Predispose Individuals to Atopic Dermatitis

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.324

7 January 2021

Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.324

7 January 2021

Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.324

7 January 2021

Identifiers

DOI

10.1038/JID.2008.324

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18987673%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

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