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

Allergy (Copenhagen), 2011-07, Vol.66 (7), p.934-940

2011

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Clumping Factor B Promotes Adherence of Staphylococcus aureus to Corneocytes in Atopic Dermatitis

Infection and immunity, 2017-06, Vol.85 (6), p.e00994-16

2017

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Atopic dermatitis increases the effect of exposure to peanut antigen in dust on peanut sensitization and likely peanut allergy

Journal of allergy and clinical immunology, 2015-01, Vol.135 (1), p.164-170.e4

2015

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A lack of premature termination codon read-through efficacy of PTC124 (Ataluren) in a diverse array of reporter assays

PLoS biology, 2013-06, Vol.11 (6), p.e1001593-e1001593

2013

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The persistence of atopic dermatitis and filaggrin ( FLG ) mutations in a US longitudinal cohort

Journal of allergy and clinical immunology, 2012-10, Vol.130 (4), p.912-917

2012

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Keratin disorders: from gene to therapy

Human molecular genetics, 2011-10, Vol.20 (2), p.R189-R197

2011

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Filaggrin loss-of-function mutations are associated with enhanced expression of IL-1 cytokines in the stratum corneum of patients with atopic dermatitis and in a murine model of filaggrin deficiency

Journal of allergy and clinical immunology, 2012-04, Vol.129 (4), p.1031-1039.e1

2012

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

Journal of allergy and clinical immunology, 2014-07, Vol.134 (1), p.82-91

2014

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One Remarkable Molecule: Filaggrin

Journal of investigative dermatology, 2012-03, Vol.132 (3), p.751-762

2012

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Mutations in GRHL2 Result in an Autosomal-Recessive Ectodermal Dysplasia Syndrome

American journal of human genetics, 2014-09, Vol.95 (3), p.308-314

2014

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

Journal of allergy and clinical immunology, 2013-07, Vol.132 (1), p.239-242.e7

2013

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Emollient enhancement of the skin barrier from birth offers effective atopic dermatitis prevention

Journal of allergy and clinical immunology, 2014-10, Vol.134 (4), p.818-823

2014

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

Journal of investigative dermatology, 2006-08, Vol.126 (8), p.1770-1775

2006

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

Journal of cell science, 2009-05, Vol.122 (9), p.1285-1294

2009

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Skin microbiome before development of atopic dermatitis: Early colonization with commensal staphylococci at 2 months is associated with a lower risk of atopic dermatitis at 1 year

Journal of allergy and clinical immunology, 2017-01, Vol.139 (1), p.166-172

2017

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Improved annotation of 3' untranslated regions and complex loci by combination of strand-specific direct RNA sequencing, RNA-Seq and ESTs

PloS one, 2014-04, Vol.9 (4), p.e94270-e94270

2014

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Lysyl Hydroxylase 3 Localizes to Epidermal Basement Membrane and Is Reduced in Patients with Recessive Dystrophic Epidermolysis Bullosa

PloS one, 2015-09, Vol.10 (9), p.e0137639-e0137639

2015

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Atopic Dermatitis and Disease Severity Are the Main Risk Factors for Food Sensitization in Exclusively Breastfed Infants

Journal of investigative dermatology, 2014-02, Vol.134 (2), p.345-350

2014

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Filaggrin Mutations Associated with Skin and Allergic Diseases

The New England journal of medicine, 2011-10, Vol.365 (14), p.1315-1327

2011

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Germline Mutation in EXPH5 Implicates the Rab27B Effector Protein Slac2-b in Inherited Skin Fragility

American journal of human genetics, 2012-12, Vol.91 (6), p.1115-1121

2012

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Development of allele-specific therapeutic siRNA in Meesmann epithelial corneal dystrophy

PloS one, 2011-12, Vol.6 (12), p.e28582-e28582

2011

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Filaggrin null mutations and childhood atopic eczema: A population-based case-control study

Journal of allergy and clinical immunology, 2008-04, Vol.121 (4), p.940-946.e3

2008

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

Clumping Factor B Promotes Adherence of Staphylococcus aureus to Corneocytes in Atopic Dermatitis

Atopic dermatitis increases the effect of exposure to peanut antigen in dust on peanut sensitization and likely peanut allergy

Atopic dermatitis is associated with an increased risk for rheumatoid arthritis and inflammatory bowel disease, and a decreased risk for type 1 diabetes

A lack of premature termination codon read-through efficacy of PTC124 (Ataluren) in a diverse array of reporter assays

The persistence of atopic dermatitis and filaggrin ( FLG ) mutations in a US longitudinal cohort

Keratin disorders: from gene to therapy

Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergy

Filaggrin loss-of-function mutations are associated with enhanced expression of IL-1 cytokines in the stratum corneum of patients with atopic dermatitis and in a murine model of filaggrin deficiency

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

Severe dermatitis, multiple allergies, and metabolic wasting syndrome caused by a novel mutation in the N-terminal plakin domain of desmoplakin

One Remarkable Molecule: Filaggrin

Mutations in GRHL2 Result in an Autosomal-Recessive Ectodermal Dysplasia Syndrome

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

Emollient enhancement of the skin barrier from birth offers effective atopic dermatitis prevention

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

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

Skin microbiome before development of atopic dermatitis: Early colonization with commensal staphylococci at 2 months is associated with a lower risk of atopic dermatitis at 1 year

Improved annotation of 3' untranslated regions and complex loci by combination of strand-specific direct RNA sequencing, RNA-Seq and ESTs

Lysyl Hydroxylase 3 Localizes to Epidermal Basement Membrane and Is Reduced in Patients with Recessive Dystrophic Epidermolysis Bullosa

Atopic Dermatitis and Disease Severity Are the Main Risk Factors for Food Sensitization in Exclusively Breastfed Infants

Filaggrin Mutations Associated with Skin and Allergic Diseases

Germline Mutation in EXPH5 Implicates the Rab27B Effector Protein Slac2-b in Inherited Skin Fragility

Development of allele-specific therapeutic siRNA in Meesmann epithelial corneal dystrophy

Filaggrin null mutations and childhood atopic eczema: A population-based case-control study

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