Heterozygous Null Alleles in Filaggrin Contribute to Clinical Dry Skin in Young Adults and the Elderly
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Filaggrin-null mutations are associated with increased maturation markers on Langerhans cells.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.Clinical presentation of atopic dermatitis by filaggrin gene mutation status during the first 7 years of life in a prospective cohort study.Contact dermatitis to topical acne drugs: a review of the literature.Sebaceous gland, hair shaft, and epidermal barrier abnormalities in keratosis pilaris with and without filaggrin deficiencyFilaggrin null mutations are not a protective factor for acne vulgaris.Skin Barrier Function and Staphylococcus aureus Colonization in Vestibulum Nasi and Fauces in Healthy Infants and Infants with Eczema: A Population-Based Cohort Study.Urea uptake enhances barrier function and antimicrobial defense in humans by regulating epidermal gene expressionOne remarkable molecule: filaggrin.Mutations in the SASPase gene (ASPRV1) are not associated with atopic eczema or clinically dry skinAcne Vulgaris and the Epidermal Barrier: Is Acne Vulgaris Associated with Inherent Epidermal Abnormalities that Cause Impairment of Barrier Functions? Do Any Topical Acne Therapies Alter the Structural and/or Functional Integrity of the Epidermal BaLevels of filaggrin degradation products are influenced by both filaggrin genotype and atopic dermatitis severity.Raman profiles of the stratum corneum define 3 filaggrin genotype-determined atopic dermatitis endophenotypes.Associations of filaggrin gene loss-of-function variants with urinary phthalate metabolites and testicular function in young Danish Men.Ichthyosis vulgaris: the filaggrin mutation disease.Cosmeceuticals based on Rhealba(®) Oat plantlet extract for the treatment of acne vulgaris.Vitamin D levels and atopic eczema in infancy and early childhood in Norway: a cohort study.Neuropathic symptoms of the ocular surface: dryness, pain, and itch.Health-related quality of life in adult dermatitis patients stratified by filaggrin genotype.Contact dermatitis in the construction industry: the role of filaggrin loss-of-function mutations.Management of patients with atopic dermatitis: the role of emollient therapy.[Genetics of common chronic inflammatory skin diseases : An update on atopic dermatitis and psoriasis].Prevalence and risk factors for xerosis in the elderly: a cross-sectional epidemiological study in primary care.Atopic dermatitis, filaggrin mutations and irritant contact dermatitis.Filaggrin compound heterozygous patients carry mutations in trans position.Xerosis is associated with asthma in men independent of atopic dermatitis and filaggrin gene mutations.Filaggrin loss-of-function mutation R501X and 2282del4 carrier status is associated with fissured skin on the hands: results from a cross-sectional population studyDisorders of Keratinization
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P2860
Heterozygous Null Alleles in Filaggrin Contribute to Clinical Dry Skin in Young Adults and the Elderly
description
im November 2008 veröffentlichter wissenschaftlicher Artikel
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scientific article published on 06 November 2008
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wetenschappelijk artikel
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наукова стаття, опублікована у квітні 2009
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name
Heterozygous Null Alleles in F ...... n Young Adults and the Elderly
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Heterozygous Null Alleles in F ...... n Young Adults and the Elderly
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type
label
Heterozygous Null Alleles in F ...... n Young Adults and the Elderly
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Heterozygous Null Alleles in F ...... n Young Adults and the Elderly
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prefLabel
Heterozygous Null Alleles in F ...... n Young Adults and the Elderly
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Heterozygous Null Alleles in F ...... n Young Adults and the Elderly
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P2093
P50
P356
P1476
Heterozygous null alleles in f ...... n young adults and the elderly
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Ann Sergeant
Colin S Munro
Frances J D Smith
Linda E Campbell
Martin Porter
P2888
P304
P356
10.1038/JID.2008.324
P407
P577
2008-11-06T00:00:00Z