(Q43433806)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21428977%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

title

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

1 reference

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26 January 2020

1 reference

11

1 reference

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26 January 2020

Irwin McLean

16

1 reference

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26 January 2020

John Common

2

1 reference

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26 January 2020

Sara J Brown

5

1 reference

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26 January 2020

author name string

H Chen

1

1 reference

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26 January 2020

R L Haines

3

1 reference

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26 January 2020

A Balakrishnan

4

1 reference

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26 January 2020

C S M Goh

6

1 reference

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26 January 2020

H J Cordell

7

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26 January 2020

A Sandilands

8

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26 January 2020

L E Campbell

9

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26 January 2020

K Kroboth

10

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26 January 2020

D L M Goh

12

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26 January 2020

M B Y Tang

13

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26 January 2020

H P van Bever

14

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26 January 2020

Y C Giam

15

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26 January 2020

E B Lane

17

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26 January 2020

language of work or name

English

0 references

publication date

1 July 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21428977%20AND%20SRC:MED&resulttype=core&format=json

British Journal of Dermatology

26 January 2020

published in

1 reference

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26 January 2020

volume

165

1 reference

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26 January 2020

issue

1

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26 January 2020

page(s)

106-114

1 reference

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

26 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

Filaggrin gene defects and risk of developing allergic sensitisation and allergic disorders: systematic review and meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

The cornified envelope: a model of cell death in the skin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

Moisturization and skin barrier function

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

A homozygous frameshift mutation in the mouse Flg gene facilitates enhanced percutaneous allergen priming.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

The prevalence and descriptive epidemiology of atopic dermatitis in Singapore school children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

FLG mutations in ichthyosis vulgaris and atopic eczema: spectrum of mutations and population genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

Atopic eczema and the filaggrin story

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

Filaggrin mutations are associated with ichthyosis vulgaris in the Bangladeshi population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

Analysis of Taiwanese ichthyosis vulgaris families further demonstrates differences in FLG mutations between European and Asian populations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

Eczema genetics: current state of knowledge and future goals

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

The U.K. Working Party's Diagnostic Criteria for Atopic Dermatitis. III. Independent hospital validation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

Practical issues on interpretation of scoring atopic dermatitis: the SCORAD index, objective SCORAD and the three-item severity score

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

Filaggrin null mutations are not a protective factor for acne vulgaris.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

Filaggrin mutations are genetic modifying factors exacerbating X-linked ichthyosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

Water modulation of stratum corneum chymotryptic enzyme activity and desquamation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

Structural and functional differences in barrier properties of African American, Caucasian and East Asian skin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

Natural moisturizing factor components in the stratum corneum as biomarkers of filaggrin genotype: evaluation of minimally invasive methods

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

Raman profiles of the stratum corneum define 3 filaggrin genotype-determined atopic dermatitis endophenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

Filaggrin null mutations and childhood atopic eczema: A population-based case-control study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

Specific Filaggrin Mutations Cause Ichthyosis Vulgaris and Are Significantly Associated with Atopic Dermatitis in Japan

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

Breaking the (Un)Sound Barrier: Filaggrin Is a Major Gene for Atopic Dermatitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

Unique and Recurrent Mutations in the Filaggrin Gene in Singaporean Chinese Patients with Ichthyosis Vulgaris

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

FLGmutation p.Lys4021X in the C-terminal imperfect filaggrin repeat in Japanese patients with atopic eczema

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

De Novo Occurrence of the Filaggrin Mutation p.R501X with Prevalent Mutation c.3321delA in a Japanese Family with Ichthyosis Vulgaris Complicated by Atopic Dermatitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2133.2011.10331.X

10.1111/J.1365-2133.2011.10331.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21428977%20AND%20SRC:MED&resulttype=core&format=json

release_gonuof237bd7jieklnlm4mj5rq

26 January 2020

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/gonuof237bd7jieklnlm4mj5rq

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

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