Filaggrin genotype determines functional and molecular alterations in skin of patients with atopic dermatitis and ichthyosis vulgaris (Q34099095)

31 July 2017

title

Filaggrin genotype determines functional and molecular alterations in skin of patients with atopic dermatitis and ichthyosis vulgaris (English)

1 reference

31 July 2017

1 reference

Maria Bradley

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31 July 2017

Hans Törmä

0 references

Magnus Nordenskjöld

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Anders Vahlquist

1 reference

31 July 2017

Mårten C G Winge

1 reference

31 July 2017

Torborg Hoppe

series ordinal

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31 July 2017

Berit Berne

series ordinal

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31 July 2017

language of work or name

English

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publication date

2 December 2011

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31 July 2017

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31 July 2017

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31 July 2017

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31 July 2017

page(s)

e28254

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Creative Commons Attribution 4.0 International

31 July 2017

start time

2 December 2011

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April 2022 Public Data File from Crossref

copyrighted

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cites work

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

1 reference

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Atopic dermatitis - from new pathophysiologic insights to individualized therapy

5 July 2018

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Levels of filaggrin degradation products are influenced by both filaggrin genotype and atopic dermatitis severity.

5 July 2018

1 reference

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5 July 2018

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ABCA12 mutations and autosomal recessive congenital ichthyosis: A review of genotype/phenotype correlations and of pathogenetic conceptsa

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STAT2 contributes to promotion of colorectal and skin carcinogenesis

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Filaggrin in the frontline: role in skin barrier function and disease

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Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources

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Global expression profiling in atopic eczema reveals reciprocal expression of inflammatory and lipid genes

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Basis for the barrier abnormality in atopic dermatitis: outside-inside-outside pathogenic mechanisms

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Large-scale identification of human genes implicated in epidermal barrier function

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

5 July 2018

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Exploration, normalization, and summaries of high density oligonucleotide array probe level data

5 July 2018

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Modulations in epidermal calcium regulate the expression of differentiation-specific markers

5 July 2018

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Vascular endothelial junction-associated molecule, a novel member of the immunoglobulin superfamily, is localized to intercellular boundaries of endothelial cells

5 July 2018

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Compound heterozygosity for an out-of-frame deletion and a splice site mutation in the LAMB3 gene causes nonlethal junctional epidermolysis bullosa

5 July 2018

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Clinical Validation and Guidelines for the SCORAD Index: Consensus Report of the European Task Force on Atopic Dermatitis

5 July 2018

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

5 July 2018

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Ultrastructural localization of calcium in psoriatic and normal human epidermis

5 July 2018

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Increased stratum corneum serine protease activity in acute eczematous atopic skin

5 July 2018

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Novel point mutation in the STS gene in a patient with X-linked recessive ichthyosis.

21 January 2018

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Skin barrier disruption by sodium lauryl sulfate-exposure alters the expressions of involucrin, transglutaminase 1, profilaggrin, and kallikreins during the repair phase in human skin in vivo

21 January 2018

1 reference

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TNF-α Downregulates Filaggrin and Loricrin through c-Jun N-terminal Kinase: Role for TNF-α Antagonists to Improve Skin Barrier

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0028254

Stratum corneum lipids, skin barrier function and filaggrin mutations in patients with atopic eczema.

21 January 2018

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Autoantibodies against CD28 are associated with atopic diseases.

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0028254

Knockdown of filaggrin impairs diffusion barrier function and increases UV sensitivity in a human skin model

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0028254

Transcriptional profiling after lipid raft disruption in keratinocytes identifies critical mediators of atopic dermatitis pathways.

21 January 2018

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Expression of a dominant negative cadherin mutant inhibits proliferation and stimulates terminal differentiation of human epidermal keratinocytes

21 January 2018

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

28 October 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0028254

Loss-of-function Variants of the Filaggrin Gene are Associated with Atopic Eczema and Associated Phenotypes in Swedish Families

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0028254

The pH gradient over the stratum corneum differs in X-linked recessive and autosomal dominant ichthyosis: a clue to the molecular origin of the "acid skin mantle"?

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22164253

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Cytokine modulation of atopic dermatitis filaggrin skin expression

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22164253

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Filaggrin repeat number polymorphism is associated with a dry skin phenotype

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22164253

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0028254

1 reference

31 July 2017

0 references

1 reference

31 July 2017

1 reference