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Carrier status for the common R501X and 2282del4 filaggrin mutations is not associated with hearing phenotypes in 5,377 children from the ALSPAC cohort

IRVINE, ALAN (2009)

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)

Current Perspectives Series: Filaggrin in Atopic Dermatitis

IRVINE, ALAN (Elsevier, 2008)

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)

Development of Allele-Specific Therapeutic siRNA in Meesmann Epithelial Corneal Dystrophy.

IRVINE, ALAN (2011)

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

IRVINE, ALAN (2014)

Tmem79/Matt is the matted mouse gene and is a predisposing gene for atopic dermatitis in human subjects

SAUNDERS, SEAN; FALLON, PADRAIC; IRVINE, ALAN (2013)

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

IRVINE, ALAN (2015)

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

IRVINE, ALAN (2015)

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Carrier status for the common R501X and 2282del4 filaggrin mutations is not associated with hearing phenotypes in 5,377 children from the ALSPAC cohort

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.

Current Perspectives Series: Filaggrin in Atopic Dermatitis

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

Development of Allele-Specific Therapeutic siRNA in Meesmann Epithelial Corneal Dystrophy.

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

Tmem79/Matt is the matted mouse gene and is a predisposing gene for atopic dermatitis in human subjects

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

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

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All of TARA

This Collection

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Carrier status for the common R501X and 2282del4 filaggrin mutations is not associated with hearing phenotypes in 5,377 children from the ALSPAC cohort

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.

Current Perspectives Series: Filaggrin in Atopic Dermatitis

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

Development of Allele-Specific Therapeutic siRNA in Meesmann Epithelial Corneal Dystrophy.

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

Tmem79/Matt is the matted mouse gene and is a predisposing gene for atopic dermatitis in human subjects

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

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