Defects of filaggrin-like proteins in both lesional and nonlesional atopic skin (Q24317035)

Filaggrin family member 2

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Filaggrin

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establishment of skin barrier

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11

Guy Serre

Guy

Serre

1 reference

3 September 2024

6

Marie-Claire Méchin

Marie-Claire

Méchin

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3 September 2024

4

Stéfana Balica

Stéfana

Balica

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3 September 2024

Laurence Pellerin

1

Laurence

Pellerin

1 reference

3 September 2024

Julie Henry

2

Julie

Henry

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3 September 2024

Chiung-Yueh Hsu

3

Chiung-Yueh

Hsu

1 reference

3 September 2024

Catherine Jean-Decoster

5

Catherine

Jean-Decoster

1 reference

3 September 2024

Britta Hansmann

7

Britta

Hansmann

1 reference

3 September 2024

Elke Rodriguez

8

Elke

Rodriguez

1 reference

3 September 2024

Stefan Weindinger

9

Stefan

Weindinger

1 reference

3 September 2024

Anne-Marie Schmitt

10

Anne-Marie

Schmitt

1 reference

3 September 2024

Carle Paul

12

Carle

Paul

1 reference

3 September 2024

Michel Simon

13

Michel

Simon

1 reference

The Journal of Allergy and Clinical Immunology

3 September 2024

language of work or name

English

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publication date

April 2013

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published in

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volume

131

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issue

4

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page(s)

1094-102

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Broad defects in epidermal cornification in atopic dermatitis identified through genomic analysis

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The 3′-UTR AACCins5874 in the stratum corneum chymotryptic enzyme gene (SCCE/KLK7), associated with atopic dermatitis; causes an increased mRNA expression without altering its stability

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Cellular and molecular mechanisms in atopic dermatitis

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Loss-of-Function Mutations in the Filaggrin Gene Lead to Reduced Level of Natural Moisturizing Factor in the Stratum Corneum

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Highly complex peptide aggregates of the S100 fused-type protein hornerin are present in human skin

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Eczema genetics: current state of knowledge and future goals

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IL-25 in atopic dermatitis: a possible link between inflammation and skin barrier dysfunction?

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Skin Barrier Function in Healthy Subjects and Patients with Atopic Dermatitis in Relation to Filaggrin Loss-of-Function Mutations

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Full Sequencing of the FLG Gene in Italian Patients with Atopic Eczema: Evidence of New Mutations, but Lack of an Association

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Association screening in the Epidermal Differentiation Complex (EDC) identifies an SPRR3 repeat number variant as a risk factor for eczema.

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

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

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Altered penetration of polyethylene glycols into uninvolved skin of atopic dermatitis patients

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Filaggrin mutations in children with severe atopic dermatitis

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Quantitative real-time reverse transcription-polymerase chain reaction analysis of drug metabolizing and cytoprotective genes in psoriasis and regulation by ultraviolet radiation.

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Atopic dermatitis: new insights and opportunities for therapeutic intervention

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Deimination of human filaggrin-2 promotes its proteolysis by calpain 1

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A milieu of regulatory elements in the epidermal differentiation complex syntenic block: implications for atopic dermatitis and psoriasis

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2,3,7,8-Tetrachlorodibenzo-p-dioxin increases the expression of genes in the human epidermal differentiation complex and accelerates epidermal barrier formation

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Hornerin is a component of the epidermal cornified cell envelopes

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Monoclonal Antibodies to Human Epidermal Filaggrin, Some Not Recognizing Profilaggrin

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Percutaneous penetration of sodium lauryl sulphate is increased in uninvolved skin of patients with atopic dermatitis compared with control subjects

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Novel filaggrin mutation but no other loss-of-function variants found in Ethiopian patients with atopic dermatitis.

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Protease-antiprotease imbalance may be linked to potential defects in profilaggrin proteolysis in atopic dermatitis

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

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Impact of filaggrin mutations on Raman spectra and biophysical properties of the stratum corneum in mild to moderate atopic dermatitis

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Atopic dermatitis: a disease of altered skin barrier and immune dysregulation

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IL-22 inhibits epidermal differentiation and induces proinflammatory gene expression and migration of human keratinocytes

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Th2 Cytokines and Atopic Dermatitis

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