Filaggrin null mutations and childhood atopic eczema: A population-based case-control study (Q57316218)

PubMed publication ID

18313126

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18313126%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

title

Filaggrin null mutations and childhood atopic eczema: a population-based case-control study (English)

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13 May 2020

1

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13 May 2020

Caroline L. Relton

2

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13 May 2020

Ian Wilson

6

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13 May 2020

John Burn

7

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13 May 2020

Nick J Reynolds

8

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13 May 2020

Irwin McLean

9

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13 May 2020

10

Heather J Cordell

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13 May 2020

5

Aileen Sandilands

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13 May 2020

3

Haihui Liao

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13 May 2020

author name string

Yiwei Zhao

4

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13 May 2020

language of work or name

English

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publication date

4 March 2008

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PubMed publication ID

18313126

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18313126%20AND%20SRC:MED&resulttype=core&format=json

The Journal of Allergy and Clinical Immunology

3 January 2020

published in

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13 May 2020

volume

121

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13 May 2020

issue

4

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13 May 2020

page(s)

940-46.e3

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

13 May 2020

cites work

1 reference

12 December 2020

Interaction of filaggrin with keratin filaments during advanced stages of normal human epidermal differentiation and in ichthyosis vulgaris

1 reference

12 December 2020

Filaggrin loss-of-function variant contributes to atopic dermatitis risk in the population of Northern Germany

1 reference

12 December 2020

Revised nomenclature for allergy for global use: Report of the Nomenclature Review Committee of the World Allergy Organization, October 2003.

1 reference

12 December 2020

Two Common Loss-of-Function Mutations within the Filaggrin Gene Predispose for Early Onset of Atopic Dermatitis

1 reference

12 December 2020

Filaggrin mutations in children with severe atopic dermatitis

1 reference

12 December 2020

The requirement for prior consent to participate on survey response rates: a population-based survey in Grampian

1 reference

12 December 2020

The atopic march: the pattern of allergic disease development in childhood

1 reference

12 December 2020

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

1 reference

12 December 2020

Skin barrier function and allergic risk

1 reference

12 December 2020

Diagnosis and treatment of atopic dermatitis in children and adults: European Academy of Allergology and Clinical Immunology/American Academy of Allergy, Asthma and Immunology/PRACTALL Consensus Report

1 reference

12 December 2020

Atopic and non-atopic eczema

1 reference

12 December 2020

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

1 reference

12 December 2020

Fleshing out filaggrin phenotypes

1 reference

12 December 2020

The natural course of atopic dermatitis from birth to age 7 years and the association with asthma

1 reference

12 December 2020

Validation of the U.K. diagnostic criteria for atopic dermatitis in a population setting. U.K. Diagnostic Criteria for Atopic Dermatitis Working Party

1 reference

12 December 2020

Decreased expression of filaggrin in atopic skin

1 reference

12 December 2020

Scoring the severity of atopic dermatitis: three item severity score as a rough system for daily practice and as a pre-screening tool for studies.

1 reference

12 December 2020

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

1 reference

12 December 2020

Clinical Features of Autosomal Dominant and Sex-linked Ichthyosis in an English Population

1 reference

12 December 2020

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

1 reference

12 December 2020

Measuring atopic eczema severity visually: which variables are most important to patients?

1 reference

12 December 2020

Proceedings of the 4th Georg Rajka International Symposium on Atopic Dermatitis, Arcachon, France, September 15-17, 2005

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

The North Cumbria Community Genetics Project

1 reference

12 December 2020

Development of the Childhood Atopic Dermatitis Impact Scale: initial validation of a quality-of-life measure for young children with atopic dermatitis and their families

1 reference

12 December 2020

The prevalence of childhood atopic eczema in a general population

1 reference

12 December 2020

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

1 reference

12 December 2020

Trends in the prevalence and severity of asthma, rhinitis and atopic eczema in 6- to 7- and 13- to 14-yr-old children from the north-east of England.

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12 December 2020

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

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12 December 2020

Moisturization and skin barrier function

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12 December 2020

The genetics of atopic dermatitis

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12 December 2020

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

1 reference

12 December 2020

10.1016/J.JACI.2008.01.013

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6978152&resulttype=core&format=json

13 May 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6978152&resulttype=core&format=json

13 May 2020

PubMed publication ID

18313126

1 reference