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Now showing items 1-10 of 49

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

IRVINE, ALAN (Company of Biologists, 2009)

Disorders of keratinisation: from rare to common genetic diseases of skin and other epithelial tissues.

IRVINE, ALAN (PubMed, 2007)

South African amaXhosa patients with atopic dermatitis have decreased levels of filaggrin breakdown products but no loss-of-function mutations in filaggrin.

IRVINE, ALAN (2014)

Current Perspectives Series: Filaggrin in Atopic Dermatitis

IRVINE, ALAN (Elsevier, 2008)

Filaggrin gene mutation associations with peanut allergy persist despite variations in peanut allergy diagnostic criteria or asthma status

IRVINE, ALAN (2013)

Filaggrin-stratified transcriptomic analysis of pediatric skin identifies mechanistic pathways in patients with atopic dermatitis.

IRVINE, ALAN (2014)

Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations.

IRVINE, ALAN (2015)

Gender- and gestational age-specific body fat percentage at birth.

IRVINE, ALAN (2011)

Filaggrin breakdown products determine corneocyte conformation in patients with atopic dermatitis.

IRVINE, ALAN (2015)

Spontaneous regression of cutaneous metastases of squamous cell carcinoma.

IRVINE, ALAN; MCMENAMIN, MAIRIN (2014)

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

Disorders of keratinisation: from rare to common genetic diseases of skin and other epithelial tissues.

South African amaXhosa patients with atopic dermatitis have decreased levels of filaggrin breakdown products but no loss-of-function mutations in filaggrin.

Current Perspectives Series: Filaggrin in Atopic Dermatitis

Filaggrin gene mutation associations with peanut allergy persist despite variations in peanut allergy diagnostic criteria or asthma status

Filaggrin-stratified transcriptomic analysis of pediatric skin identifies mechanistic pathways in patients with atopic dermatitis.

Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations.

Gender- and gestational age-specific body fat percentage at birth.

Filaggrin breakdown products determine corneocyte conformation in patients with atopic dermatitis.

Spontaneous regression of cutaneous metastases of squamous cell carcinoma.

Browse

All of TARA

This Collection

Discover

Author

Subject

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

Disorders of keratinisation: from rare to common genetic diseases of skin and other epithelial tissues.

South African amaXhosa patients with atopic dermatitis have decreased levels of filaggrin breakdown products but no loss-of-function mutations in filaggrin.

Current Perspectives Series: Filaggrin in Atopic Dermatitis

Filaggrin gene mutation associations with peanut allergy persist despite variations in peanut allergy diagnostic criteria or asthma status

Filaggrin-stratified transcriptomic analysis of pediatric skin identifies mechanistic pathways in patients with atopic dermatitis.

Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations.

Gender- and gestational age-specific body fat percentage at birth.

Filaggrin breakdown products determine corneocyte conformation in patients with atopic dermatitis.

Spontaneous regression of cutaneous metastases of squamous cell carcinoma.