Filaggrin gene mutation c.3321delA is associated with various clinical features of atopic dermatitis in the Chinese Han population.
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Genetic and epigenetic studies of atopic dermatitisFilaggrin silencing by shRNA directly impairs the skin barrier function of normal human epidermal keratinocytes and then induces an immune responseFilaggrin Gene Mutation c.3321delA is Associated with Dry Phenotypes of Atopic Dermatitis in the Chinese Han PopulationFilaggrin Mutation in Korean Patients with Atopic Dermatitis.Qualitative vs. quantitative atopic dermatitis criteria - in historical and present perspectives.Clinical characteristics of Korean patients with filaggrin-related atopic dermatitis.Association of FLG single nucleotide variations with clinical phenotypes of atopic dermatitis.Development of Unlabeled Probe Based High-Resolution Melting Analysis for Detection of Filaggrin Gene Mutation c.3321delA.
P2860
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P2860
Filaggrin gene mutation c.3321delA is associated with various clinical features of atopic dermatitis in the Chinese Han population.
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2014 nî lūn-bûn
@nan
2014 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Filaggrin gene mutation c.3321 ...... in the Chinese Han population.
@ast
Filaggrin gene mutation c.3321 ...... in the Chinese Han population.
@en
type
label
Filaggrin gene mutation c.3321 ...... in the Chinese Han population.
@ast
Filaggrin gene mutation c.3321 ...... in the Chinese Han population.
@en
prefLabel
Filaggrin gene mutation c.3321 ...... in the Chinese Han population.
@ast
Filaggrin gene mutation c.3321 ...... in the Chinese Han population.
@en
P2093
P2860
P1433
P1476
Filaggrin gene mutation c.3321 ...... in the Chinese Han population.
@en
P2093
Changbing Shen
Dawei Duan
Huayang Tang
Jinhua Zhao
P2860
P304
P356
10.1371/JOURNAL.PONE.0098235
P407
P577
2014-05-23T00:00:00Z