Heritable filaggrin disorders: the paradigm of atopic dermatitis (Q34312026)

1 August 2017

Heritable filaggrin disorders: the paradigm of atopic dermatitis (English)

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1 August 2017

Alan D Irvine

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author name string

W H Irwin McLean

series ordinal

1

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PubMed ID

23154627

1 August 2017

language of work or name

English

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publication date

15 November 2012

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Journal of Investigative Dermatology

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1 August 2017

132

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1 August 2017

E1

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1 August 2017

E20-1

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https://scigraph.springernature.com/pub.10.1038/skinbio.2012.6

1 August 2017

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cites work

Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergy.

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7 January 2021

Intragenic copy number variation within filaggrin contributes to the risk of atopic dermatitis with a dose-dependent effect

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https://api.crossref.org/works/10.1038%2FSKINBIO.2012.6

7 January 2021

Wide spectrum of filaggrin-null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populations.

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https://api.crossref.org/works/10.1038%2FSKINBIO.2012.6

7 January 2021

Purification and characterization of a basic protein from the stratum corneum of mammalian epidermis

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7 January 2021

Assembly of stratum corneum basic protein and keratin filaments in macrofibrils

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https://api.crossref.org/works/10.1038%2FSKINBIO.2012.6

7 January 2021

A homozygous frameshift mutation in the mouse Flg gene facilitates enhanced percutaneous allergen priming.

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https://api.crossref.org/works/10.1038%2FSKINBIO.2012.6

7 January 2021

Filaggrin genotype in ichthyosis vulgaris predicts abnormalities in epidermal structure and function

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https://api.crossref.org/works/10.1038%2FSKINBIO.2012.6

7 January 2021

Cytokine modulation of atopic dermatitis filaggrin skin expression

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https://api.crossref.org/works/10.1038%2FSKINBIO.2012.6

7 January 2021

Fleshing out filaggrin phenotypes

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https://api.crossref.org/works/10.1038%2FSKINBIO.2012.6

7 January 2021

Breaking the (Un)Sound Barrier: Filaggrin Is a Major Gene for Atopic Dermatitis

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https://api.crossref.org/works/10.1038%2FSKINBIO.2012.6

7 January 2021

Filaggrin mutations associated with skin and allergic diseases.

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https://api.crossref.org/works/10.1038%2FSKINBIO.2012.6

7 January 2021

Stratum corneum lipids, skin barrier function and filaggrin mutations in patients with atopic eczema.

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https://api.crossref.org/works/10.1038%2FSKINBIO.2012.6

7 January 2021

Changes in environmental humidity affect the water-holding property of the stratum corneum and its free amino acid content, and the expression of filaggrin in the epidermis of hairless mice

1 reference

https://api.crossref.org/works/10.1038%2FSKINBIO.2012.6

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%2FSKINBIO.2012.6

7 January 2021

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.

1 reference

https://api.crossref.org/works/10.1038%2FSKINBIO.2012.6

7 January 2021

Levels of filaggrin degradation products are influenced by both filaggrin genotype and atopic dermatitis severity.

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https://api.crossref.org/works/10.1038%2FSKINBIO.2012.6

7 January 2021

Effect of filaggrin breakdown products on growth of and protein expression by Staphylococcus aureus

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https://api.crossref.org/works/10.1038%2FSKINBIO.2012.6

7 January 2021

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

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https://api.crossref.org/works/10.1038%2FSKINBIO.2012.6

7 January 2021

Meta-analysis of filaggrin polymorphisms in eczema and asthma: Robust risk factors in atopic disease

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https://api.crossref.org/works/10.1038%2FSKINBIO.2012.6

7 January 2021

Filaggrin in the frontline: role in skin barrier function and disease

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https://api.crossref.org/works/10.1038%2FSKINBIO.2012.6

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%2FSKINBIO.2012.6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSKINBIO.2012.6

7 January 2021

Ichthyosis vulgaris: identification of a defect in synthesis of filaggrin correlated with an absence of keratohyaline granules

1 reference

https://api.crossref.org/works/10.1038%2FSKINBIO.2012.6

7 January 2021

Identifiers

DOI

10.1038/SKINBIO.2012.6

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PubMed ID

23154627

Dimensions Publication ID

1 August 2017

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