Filaggrin failure - from ichthyosis vulgaris to atopic eczema and beyond - Wikidata - awgldk - TriplyDB

Filaggrin failure - from ichthyosis vulgaris to atopic eczema and beyond

Filaggrin failure - from ichthyosis vulgaris to atopic eczema and beyond

http://www.wikidata.org/entity/Q28079701

about

Prescriptions for atopic dermatitis: oral corticosteroids remain commonplace.Loss of epidermal AP1 transcription factor function reduces filaggrin level, alters chemokine expression and produces an ichthyosis-related phenotype.Embryonic AP1 Transcription Factor Deficiency Causes a Collodion Baby-Like Phenotype Novel role for the testis-enriched HSPA2 protein in regulating epidermal keratinocyte differentiation.Skin microbiota-host interactions.Atopic Dermatitis: Disease Background and Risk Factors.Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment.Air exposure may be associated with the histological differentiation of a cultured epidermal autograft (JACE).

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P2860

Filaggrin failure - from ichthyosis vulgaris to atopic eczema and beyond

http://www.wikidata.org/entity/Q28079701

description

2016 nî lūn-bûn

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2016 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2016 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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name

Filaggrin failure - from ichthyosis vulgaris to atopic eczema and beyond

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Filaggrin failure - from ichthyosis vulgaris to atopic eczema and beyond

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Filaggrin failure - from ichthyosis vulgaris to atopic eczema and beyond

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Filaggrin failure - from ichthyosis vulgaris to atopic eczema and beyond

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Filaggrin failure - from ichthyosis vulgaris to atopic eczema and beyond

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Filaggrin failure - from ichthyosis vulgaris to atopic eczema and beyond

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Filaggrin failure - from ichthyosis vulgaris to atopic eczema and beyond

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Filaggrin failure - from ichthyosis vulgaris to atopic eczema and beyond

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Filaggrin failure - from ichthyosis vulgaris to atopic eczema and beyond

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P1433

British Journal of Dermatology

P1476

Filaggrin failure - from ichthyosis vulgaris to atopic eczema and beyond

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P2093

W.H.I. McLean

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P2860

Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

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

Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization

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

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

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

Filaggrin mutations associated with skin and allergic diseases.

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

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

Regulated expression of human filaggrin in keratinocytes results in cytoskeletal disruption, loss of cell-cell adhesion, and cell cycle arrest.

P304

4-7

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P31

scholarly article

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3227114

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P356

10.1111/BJD.14997

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P478

175 Suppl 2

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P577

2016-10-01T00:00:00Z

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27667308

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5053269

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