Loss-of-function mutations in the filaggrin gene and allergic contact sensitization to nickel.
about
Mechanisms of abnormal lamellar body secretion and the dysfunctional skin barrier in patients with atopic dermatitisMutations in the filaggrin gene and food allergyFilaggrin deficiency confers a paracellular barrier abnormality that reduces inflammatory thresholds to irritants and haptensAnchoring molecular mechanisms to the adverse outcome pathway for skin sensitization: Analysis of existing data.Filaggrin gene mutation c.3321delA is associated with various clinical features of atopic dermatitis in the Chinese Han population.Abnormal skin barrier in the etiopathogenesis of atopic dermatitis.An update on the genetics of atopic dermatitis: scratching the surface in 2009.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.Contact allergy and allergic contact dermatitis in children - a review of current data.Contact allergens in a pediatric population: association with atopic dermatitis and comparison with other north american referral centersPeanut allergy: effect of environmental peanut exposure in children with filaggrin loss-of-function mutations.Atopic dermatitis results in intrinsic barrier and immune abnormalities: implications for contact dermatitis.Possible participation of acidic pH in bone resorption in middle ear cholesteatoma.Metal allergy and systemic contact dermatitis: an overview.One remarkable molecule: filaggrin.Early immune events in the induction of allergic contact dermatitisRaman profiles of the stratum corneum define 3 filaggrin genotype-determined atopic dermatitis endophenotypes.The stratum corneum comprises three layers with distinct metal-ion barrier properties.Filaggrin mutations that confer risk of atopic dermatitis confer greater risk for eczema herpeticum.Filaggrin gene mutations are associated with asthma and eczema in later lifeGuanine nucleotide exchange factor RABGEF1 regulates keratinocyte-intrinsic signaling to maintain skin homeostasisDoes eczema lead to asthma?Impact of atopic dermatitis and loss-of-function mutations in the filaggrin gene on the development of occupational irritant contact dermatitis.Diagnostic approach in allergic and irritant contact dermatitis.Therapeutic Implications of a Barrier-based Pathogenesis of Atopic Dermatitis.Therapeutic implications of a barrier-based pathogenesis of atopic dermatitisAtopic dermatitis - from new pathophysiologic insights to individualized therapy.Nickel allergies: paying the Toll for innate immunity.Epidermal barrier dysfunction and cutaneous sensitization in atopic diseases.The many faces of nickel allergy.Coin exposure may cause allergic nickel dermatitis: a review.Ichthyosis vulgaris: the filaggrin mutation disease.The stratum corneum: the rampart of the mammalian body.Allergic contact dermatitis in children: which factors are relevant? (review of the literature).Immunology of atopic eczema: overcoming the Th1/Th2 paradigm.Lipid abnormalities and lipid-based repair strategies in atopic dermatitis.The multiple factors affecting the association between atopic dermatitis and contact sensitization.Atopic dermatitis and the stratum corneum: part 3: the immune system in atopic dermatitis.Evolving concepts of neonatal skin.Novel FLG null mutations in Korean patients with atopic dermatitis and comparison of the mutational spectra in Asian populations.
P2860
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P2860
Loss-of-function mutations in the filaggrin gene and allergic contact sensitization to nickel.
description
2007 nî lūn-bûn
@nan
2007 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Loss-of-function mutations in ...... ntact sensitization to nickel.
@ast
Loss-of-function mutations in ...... ntact sensitization to nickel.
@en
Loss-of-function mutations in ...... ntact sensitization to nickel.
@nl
type
label
Loss-of-function mutations in ...... ntact sensitization to nickel.
@ast
Loss-of-function mutations in ...... ntact sensitization to nickel.
@en
Loss-of-function mutations in ...... ntact sensitization to nickel.
@nl
prefLabel
Loss-of-function mutations in ...... ntact sensitization to nickel.
@ast
Loss-of-function mutations in ...... ntact sensitization to nickel.
@en
Loss-of-function mutations in ...... ntact sensitization to nickel.
@nl
P2093
P50
P356
P1476
Loss-of-function mutations in ...... ntact sensitization to nickel.
@en
P2093
Elke Rodriguez
Heidrun Behrendt
Johannes Ring
Natalija Novak
Stefan Wagenpfeil
Torsten Schäfer
P2888
P304
P356
10.1038/SJ.JID.5701190
P407
P577
2007-11-29T00:00:00Z
P5875
P6179
1049799371