(Q58859837)

2

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Aileen Sandilands

3

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Yuin Chew Chan

4

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Yoke Chin Giam

5

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Alan T. Evans

6

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E. Birgitte Lane

7

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W. H Irwin McLean

Journal of Investigative Dermatology

8

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language of work or name

English

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publication date

July 2008

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published in

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volume

128

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issue

7

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page(s)

1669-1675

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exact match

https://scigraph.springernature.com/pub.10.1038/jid.2008.2

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cites work

Null Mutations in the Filaggrin Gene (FLG) Determine Major Susceptibility to Early-Onset Atopic Dermatitis that Persists into Adulthood

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.2

7 January 2021

Are atopy and palm-sole hyperlinearity clinical tools in the differential diagnosis between ichthyosis vulgaris and X-linked ichthyosis?

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.2

7 January 2021

Filaggrin mutations p.R501X and c.2282del4 in ichthyosis vulgaris

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.2

7 January 2021

Fleshing out filaggrin phenotypes

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.2

7 January 2021

Filaggrin mutations are genetic modifying factors exacerbating X-linked ichthyosis.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.2

7 January 2021

Filaggrin loss-of-function mutations predispose to phenotypes involved in the atopic march.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.2

7 January 2021

Genes encoding structural proteins of epidermal cornification and S100 calcium-binding proteins form a gene complex ("epidermal differentiation complex") on human chromosome 1q21

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.2

7 January 2021

Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.2

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.2008.2

7 January 2021

Moisturization and skin barrier function

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.2

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.2008.2

7 January 2021

Enzymatic basis of typical X-linked icthyosis

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.2

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.2008.2

7 January 2021

Two Common Loss-of-Function Mutations within the Filaggrin Gene Predispose for Early Onset of Atopic Dermatitis

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.2

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%2FJID.2008.2

7 January 2021

The prevalence and descriptive epidemiology of atopic dermatitis in Singapore school children.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.2

7 January 2021

https://api.crossref.org/works/10.1038%2FJID.2008.2

1 reference

7 January 2021