(Q37138571)

18 August 2017

1 reference

title

Filaggrin and the great epidermal barrier grief (English)

1 reference

18 August 2017

0 references

John A McGrath

1

1 reference

18 August 2017

1 May 2008

1 reference

Australasian Journal of Dermatology

18 August 2017

1 reference

18 August 2017

49

1 reference

18 August 2017

2

1 reference

18 August 2017

67-73; quiz 73-4

1 reference

A current and online genodermatosis database

18 August 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

Translational benefits from research on rare genodermatoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

Filaggrin's fuller figure: a glimpse into the genetic architecture of atopic dermatitis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

Neonatal skin barrier: structure, function, and disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

The skin barrier in healthy and diseased state

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

The cornified envelope: a model of cell death in the skin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

Genetic linkage of childhood atopic dermatitis to psoriasis susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

Large-scale identification of human genes implicated in epidermal barrier function

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

Cytokine modulation of atopic dermatitis filaggrin skin expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

Filaggrin null mutations are associated with increased asthma severity in children and young adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

Filaggrin null alleles are not associated with psoriasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

Autoantibodies to citrullinated proteins: ACPA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

Chemical biology: ignore the nonsense.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

Simultaneous effect of ursolic acid and oleanolic acid on epidermal permeability barrier function and epidermal keratinocyte differentiation via peroxisome proliferator-activated receptor-alpha

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

Loss-of-Function Mutations in the Filaggrin Gene and Alopecia Areata: Strong Risk Factor for a Severe Course of Disease in Patients Comorbid for Atopic Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

Loss-of-function mutations in the filaggrin gene: no contribution to disease susceptibility, but to autoantibody formation against citrullinated peptides in early rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-0960.2008.00443.X

10.1111/J.1440-0960.2008.00443.X

21 January 2018

Identifiers

DOI

1 reference

18 August 2017

1 reference

PubMed ID

18412804