(Q57638950)

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

25 December 2019

title

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

1 reference

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25 December 2019

1 reference

3

1 reference

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25 December 2019

Colin Palmer

5

1 reference

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25 December 2019

Irwin McLean

7

1 reference

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25 December 2019

author name string

Ann Sergeant

1

1 reference

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25 December 2019

Martin Porter

4

1 reference

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25 December 2019

Linda E Campbell

2

1 reference

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25 December 2019

Frances J D Smith

6

1 reference

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25 December 2019

Colin S Munro

8

1 reference

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25 December 2019

language of work or name

English

0 references

publication date

6 November 2008

1 reference

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

Journal of Investigative Dermatology

25 December 2019

published in

1 reference

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25 December 2019

volume

129

1 reference

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25 December 2019

issue

4

1 reference

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25 December 2019

page(s)

1042-1045

1 reference

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

25 December 2019

exact match

0 references

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

1 reference

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

25 December 2019

1 reference