Novel filaggrin mutation but no other loss-of-function variants found in Ethiopian patients with atopic dermatitis.
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Molecular Genetic of Atopic dermatitis: An UpdateImmune Pathways in Atopic Dermatitis, and Definition of Biomarkers through Broad and Targeted TherapeuticsGenetic and epigenetic studies of atopic dermatitisEvidence That Loss-of-Function Filaggrin Gene Mutations Evolved in Northern Europeans to Favor Intracutaneous Vitamin D3 ProductionExome sequencing of filaggrin and related genes in African-American children with atopic dermatitis.Sebaceous gland, hair shaft, and epidermal barrier abnormalities in keratosis pilaris with and without filaggrin deficiencyFilaggrin silencing by shRNA directly impairs the skin barrier function of normal human epidermal keratinocytes and then induces an immune responseOne remarkable molecule: filaggrin.Association of HLA-DRB1 genetic variants with the persistence of atopic dermatitis.The persistence of atopic dermatitis and filaggrin (FLG) mutations in a US longitudinal cohortIn a three-dimensional reconstructed human epidermis filaggrin-2 is essential for proper cornification.Filaggrin-2 variation is associated with more persistent atopic dermatitis in African American subjects.Ichthyosis vulgaris: the filaggrin mutation disease.Atopic dermatitis in different skin types. What is to know?Unravelling the complex genetic background of atopic dermatitis: from genetic association results towards novel therapeutic strategies.Resolving the etiology of atopic disorders by using genetic analysis of racial ancestry.Immunologic Targets in Atopic Dermatitis and Emerging Therapies: An Update.Tight junctions in skin inflammation.The tight junction gene Claudin-1 is associated with atopic dermatitis among Ethiopians.It Remains Unknown Whether Filaggrin Gene Mutations Evolved to Increase Cutaneous Synthesis of Vitamin DAtopic Dermatitis Susceptibility Variants in Filaggrin Hitchhike Hornerin Selective Sweep.South African amaXhosa patients with atopic dermatitis have decreased levels of filaggrin breakdown products but no loss-of-function mutations in filaggrin.Basis for the gain and subsequent dilution of epidermal pigmentation during human evolution: The barrier and metabolic conservation hypotheses revisited.Lack of association between filaggrin gene mutations and onset of psoriasis in childhood.Association of KIF3A, but not OVOL1 and ACTL9, with atopic eczema in Italian patients.Filaggrin mutation mapping in the African population.Atopic Dermatitis: Disease Background and Risk Factors.Loss-of-function mutations in filaggrin gene associate with psoriasis vulgaris in Chinese population.8th Georg Rajka International Symposium on Atopic Dermatitis: meeting report.Filaggrin gene mutations in African Americans with both ichthyosis vulgaris and atopic dermatitis.
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P2860
Novel filaggrin mutation but no other loss-of-function variants found in Ethiopian patients with atopic dermatitis.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh-hant
name
Novel filaggrin mutation but n ...... tients with atopic dermatitis.
@en
Novel filaggrin mutation but n ...... tients with atopic dermatitis.
@nl
type
label
Novel filaggrin mutation but n ...... tients with atopic dermatitis.
@en
Novel filaggrin mutation but n ...... tients with atopic dermatitis.
@nl
prefLabel
Novel filaggrin mutation but n ...... tients with atopic dermatitis.
@en
Novel filaggrin mutation but n ...... tients with atopic dermatitis.
@nl
P2093
P2860
P50
P1476
Novel filaggrin mutation but n ...... atients with atopic dermatitis
@en
P2093
A Sandilands
C-F Wahlgren
D Shibeshi
K D Bilcha
P2860
P304
P356
10.1111/J.1365-2133.2011.10475.X
P407
P577
2011-10-17T00:00:00Z