Comprehensive screening for a complete set of Japanese-population-specific filaggrin gene mutations. - Wikidata - awgldk - TriplyDB

Comprehensive screening for a complete set of Japanese-population-specific filaggrin gene mutations.

Comprehensive screening for a complete set of Japanese-population-specific filaggrin gene mutations.

http://www.wikidata.org/entity/Q40219992

about

Highly prevalent LIPH founder mutations causing autosomal recessive woolly hair/hypotrichosis in Japan and the genotype/phenotype correlations Update on skin allergy.Latest developments in allergic rhinitis in Allergy for clinicians and researchers.The immunology of atopic dermatitis and its reversibility with broad-spectrum and targeted therapies.Inherited ichthyosis: Non-syndromic forms.IgE-associated allergic disorders: recent advances in etiology, diagnosis, and treatment.Skin steroidogenesis in health and disease.A rare variant in CYP27A1 and its association with atopic dermatitis with high serum total IgE.Ripple-pattern lichen amyloidosis in a case of ichthyosis vulgaris with a novel FLG mutation.A severe case of X-linked ichthyosis showing palmar hyperlinearity without FLG mutations.Development of Unlabeled Probe Based High-Resolution Melting Analysis for Detection of Filaggrin Gene Mutation c.3321delA.Hyper-IgE syndrome with a novel mutation of the STAT3 gene.

P2860

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P2860

Comprehensive screening for a complete set of Japanese-population-specific filaggrin gene mutations.

http://www.wikidata.org/entity/Q40219992

description

2014 nî lūn-bûn

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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2014年论文

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2014年论文

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name

Comprehensive screening for a ...... ific filaggrin gene mutations.

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Comprehensive screening for a ...... ific filaggrin gene mutations.

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Comprehensive screening for a ...... ific filaggrin gene mutations.

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Comprehensive screening for a ...... ific filaggrin gene mutations.

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H Shimizu

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H Tsujiuchi

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M Akiyama

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M Kono

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N Hamajima

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O Mizuno

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S Suzuki

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Y Ohguchi

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P2860

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

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

The multifunctional role of filaggrin in allergic skin disease.

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

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

Significant association between methylenetetrahydrofolate reductase 677T allele and hyperuricemia among adult Japanese subjects.

Japanese-specific filaggrin gene mutations in Japanese patients suffering from atopic eczema and asthma.

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

Atopic diseases by filaggrin mutations and birth year.

Prevalent and Rare Mutations in the Gene Encoding Filaggrin in Japanese Patients with Ichthyosis Vulgaris and Atopic Dermatitis

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537-540

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scholarly article

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10.1111/ALL.12369

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4

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69

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Toshifumi Nomura

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2014-01-28T00:00:00Z

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24467288

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