about
Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanismsTmem79/Matt is the matted mouse gene and is a predisposing gene for atopic dermatitis in human subjectsSilk garments plus standard care compared with standard care for treating eczema in children: A randomised, controlled, observer-blind, pragmatic trial (CLOTHES Trial).Filaggrin-stratified transcriptomic analysis of pediatric skin identifies mechanistic pathways in patients with atopic dermatitis.Filaggrin haploinsufficiency is highly penetrant and is associated with increased severity of eczema: further delineation of the skin phenotype in a prospective epidemiological study of 792 school children.Emollient enhancement of the skin barrier from birth offers effective atopic dermatitis preventionPeanut allergy: effect of environmental peanut exposure in children with filaggrin loss-of-function mutations.Chromosome 11q13.5 variant associated with childhood eczema: an effect supplementary to filaggrin mutationsAtopic dermatitis increases the effect of exposure to peanut antigen in dust on peanut sensitization and likely peanut allergy.Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergy.Filaggrin null mutations are not a protective factor for acne vulgaris.Improved annotation of 3' untranslated regions and complex loci by combination of strand-specific direct RNA sequencing, RNA-Seq and ESTs.Intragenic copy number variation within filaggrin contributes to the risk of atopic dermatitis with a dose-dependent effectOne remarkable molecule: filaggrin.Mutations in the SASPase gene (ASPRV1) are not associated with atopic eczema or clinically dry skinHigh-density genotyping study identifies four new susceptibility loci for atopic dermatitis.A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis.Identification of translational dermatology research priorities in the U.K.: results of an electronic Delphi exerciseHaploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma.Eczema genetics: current state of knowledge and future goals.Propranolol in the treatment of infantile haemangiomas: lessons from the European Propranolol In the Treatment of Complicated Haemangiomas (PITCH) Taskforce survey.Hand dermatitis in construction workers: a lesson in genetic epidemiology.Filaggrin gene mutation associations with peanut allergy persist despite variations in peanut allergy diagnostic criteria or asthma statusSouth African amaXhosa patients with atopic dermatitis have decreased levels of filaggrin breakdown products but no loss-of-function mutations in filaggrin.Heterozygous mutations in AAGAB cause type 1 punctate palmoplantar keratoderma with evidence for increased growth factor signaling.Wide spectrum of filaggrin-null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populations.Subcorneal pustular dermatosis in association with chronic lymphocytic leukaemia.Coma blisters in 2 children on anticonvulsant medication.The Microevolution and Epidemiology of Staphylococcus aureus Colonization during Atopic Eczema Disease Flare.Filaggrin loss-of-function variants are associated with atopic comorbidity in pediatric inflammatory bowel disease.The pharmacogenetics of body odor: as easy as ABCC?Prevalent and Low-Frequency Null Mutations in the Filaggrin Gene Are Associated with Early-Onset and Persistent Atopic EczemaFilaggrin null mutations and childhood atopic eczema: A population-based case-control studyLoss-of-Function Mutations in the Gene Encoding Filaggrin Are Not Strongly Associated with Chronic Actinic DermatitisInsight from the Air–Skin InterfaceMeta-analysis of filaggrin polymorphisms in eczema and asthma: Robust risk factors in atopic diseaseAre filaggrin mutations associated with hand eczema or contact allergy? – we do not knowPseudoxanthoma elasticum: biopsy of clinically normal skin in the investigation of patients with angioid streaksChronic cutaneous graft-versus-host disease associated with multiple cutaneous squamous cell carcinomasEvidence of a causal relationship between body mass index and psoriasis: A mendelian randomization study
P50
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P50
description
hulumtuese
@sq
researcher
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wetenschapper
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հետազոտող
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name
Sara J Brown
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Sara J Brown
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Sara J Brown
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Sara J Brown
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Sara J Brown
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type
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Sara J Brown
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Sara J Brown
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Sara J Brown
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Sara J Brown
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Sara J Brown
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Sara Brown
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Sara J Brown
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Sara J Brown
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Sara J Brown
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Sara J Brown
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Sara J Brown
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P106
P21
P31
P496
0000-0002-3232-5251