Filaggrin gene mutation c.3321delA is associated with various clinical features of atopic dermatitis in the Chinese Han population (Q33655186)

28 July 2017

title

Filaggrin gene mutation c.3321delA is associated with various clinical features of atopic dermatitis in the Chinese Han population (English)

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28 July 2017

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Li Meng

1

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28 July 2017

Li Wang

2

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28 July 2017

Huayang Tang

3

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28 July 2017

Xianfa Tang

4

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28 July 2017

Xiaoyun Jiang

5

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28 July 2017

Jinhua Zhao

6

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28 July 2017

Jing Gao

7

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28 July 2017

Bing Li

8

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28 July 2017

Xuhui Fu

9

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28 July 2017

Yan Chen

10

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28 July 2017

Weiyi Yao

11

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28 July 2017

Wenying Zhan

12

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28 July 2017

Bo Wu

13

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28 July 2017

Dawei Duan

14

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28 July 2017

Changbing Shen

15

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28 July 2017

Hui Cheng

16

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28 July 2017

Xianbo Zuo

17

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28 July 2017

Sen Yang

18

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28 July 2017

Liangdan Sun

19

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28 July 2017

Xuejun Zhang

20

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28 July 2017

language of work or name

English

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publication date

23 May 2014

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28 July 2017

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28 July 2017

volume

9

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28 July 2017

issue

5

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28 July 2017

page(s)

e98235

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Creative Commons Attribution 4.0 International

28 July 2017

copyright license

start time

23 May 2014

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Common FLG mutation K4671X not associated with atopic dermatitis in Han Chinese in a family association study

21 June 2018

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Association analysis of single nucleotide polymorphisms at five loci: comparison between atopic dermatitis and asthma in the Chinese Han population

21 June 2018

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21 June 2018

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Filaggrin genotype in ichthyosis vulgaris predicts abnormalities in epidermal structure and function

21 June 2018

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Filaggrin gene defects are independent risk factors for atopic asthma in a Polish population: a study in ECAP cohort

21 June 2018

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21 June 2018

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Filaggrin mutations in the onset of eczema, sensitization, asthma, hay fever and the interaction with cat exposure

21 June 2018

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Filaggrin deficiency confers a paracellular barrier abnormality that reduces inflammatory thresholds to irritants and haptens

21 June 2018

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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.

21 June 2018

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Filaggrin mutations, atopic eczema, hay fever, and asthma in children

21 June 2018

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The burden of disease associated with filaggrin mutations: a population-based, longitudinal birth cohort study

21 June 2018

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Loss-of-function mutations in the filaggrin gene and allergic contact sensitization to nickel

21 June 2018

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Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations

21 June 2018

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Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris.

21 June 2018

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Atopic dermatitis and the atopic march

21 June 2018

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Severity scoring of atopic dermatitis: the SCORAD index. Consensus Report of the European Task Force on Atopic Dermatitis

21 June 2018

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Stratum corneum hydration and amino acid content in xerotic skin.

21 June 2018

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Mutations analysis in filaggrin gene in northern China patients with atopic dermatitis

21 June 2018

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Wide spectrum of filaggrin-null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populations.

21 January 2018

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Null Mutations in the Filaggrin Gene (FLG) Determine Major Susceptibility to Early-Onset Atopic Dermatitis that Persists into Adulthood

21 January 2018

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Analysis of four prevalent filaggrin mutations (R501X, 2282del4, R2447X and S3247X) in Austrian and German patients with atopic dermatitis

21 January 2018

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Prevalent and Low-Frequency Null Mutations in the Filaggrin Gene Are Associated with Early-Onset and Persistent Atopic Eczema

21 January 2018

1 reference

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An action spectrum for the production of cis-urocanic acid in human skin in vivo

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0098235

Filaggrin loss-of-function mutations predispose to phenotypes involved in the atopic march.

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0098235

Is eczema really on the increase worldwide?

21 January 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4032331

The prevalence of accentuated palmoplantar markings and keratosis pilaris in atopic dermatitis, autosomal dominant ichthyosis and control dermatological patients

30 October 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4032331

Association between Loss-of-Function Mutations in the Filaggrin Gene and Self-Reported Food Allergy and Alcohol Sensitivity

30 October 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0098235

Prevalent and Rare Mutations in the Gene Encoding Filaggrin Cause Ichthyosis Vulgaris and Predispose Individuals to Atopic Dermatitis

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0098235

Association analysis of filaggrin gene mutations and atopic dermatitis in Northern China

21 January 2018

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12 December 2020

Mutations in the filaggrin gene in Han Chinese patients with atopic dermatitis

1 reference

12 December 2020

Genome-wide association study identifies two new susceptibility loci for atopic dermatitis in the Chinese Han population

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12 December 2020

Effects of aging and xerosis on the amino acid composition of human skin

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12 December 2020

Filaggrin repeat number polymorphism is associated with a dry skin phenotype

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12 December 2020

Filaggrin mutations strongly predispose to early-onset and extrinsic atopic dermatitis

1 reference

12 December 2020

Filaggrin mutations in children with severe atopic dermatitis

1 reference

12 December 2020

Filaggrin null mutations are associated with atopic dermatitis and elevated levels of IgE in the Japanese population: a family and case-control study

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0098235

Identifiers

DOI

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28 July 2017

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28 July 2017

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