Development of ichthyosiform skin compensates for defective permeability barrier function in mice lacking transglutaminase 1 - Wikidata - wikimedia - TriplyDB

Development of ichthyosiform skin compensates for defective permeability barrier function in mice lacking transglutaminase 1

Development of ichthyosiform skin compensates for defective permeability barrier function in mice lacking transglutaminase 1

http://www.wikidata.org/entity/Q34786940

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Skin-derived TSLP triggers progression from epidermal-barrier defects to asthma Nonsyndromic types of ichthyoses - an update Epidermal transglutaminase (TGase 3) is required for proper hair development, but not the formation of the epidermal barrier A novel transglutaminase activator forms a complex with type 1 transglutaminase Novel transglutaminase 1 mutations in patients affected by lamellar ichthyosis.Transglutaminase-1 gene mutations in autosomal recessive congenital ichthyosis: summary of mutations (including 23 novel) and modeling of TGase-1 Epidermal ADAM17 maintains the skin barrier by regulating EGFR ligand-dependent terminal keratinocyte differentiation.Ets1 induces dysplastic changes when expressed in terminally-differentiating squamous epidermal cells Epidermal barrier defects link atopic dermatitis with altered skin cancer susceptibility Self-improvement of keratinocyte differentiation defects during skin maturation in ABCA12-deficient harlequin ichthyosis model mice.Type I transglutaminase accumulation in the endoplasmic reticulum may be an underlying cause of autosomal recessive congenital ichthyosis.Effects of in utero exposure of C57BL/6J mice to 2,3,7,8-tetrachlorodibenzo-p-dioxin on epidermal permeability barrier development and function Epidermal barrier formation and recovery in skin disorders.Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development.Periplakin gene targeting reveals a constituent of the cornified cell envelope dispensable for normal mouse development.Role of taurine in the vasculature: an overview of experimental and human studies.Topical hesperidin improves epidermal permeability barrier function and epidermal differentiation in normal murine skin.Long-term faithful recapitulation of transglutaminase 1-deficient lamellar ichthyosis in a skin-humanized mouse model, and insights from proteomic studies A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity.Mice deficient in involucrin, envoplakin, and periplakin have a defective epidermal barrier Ichthyosis update: towards a function-driven model of pathogenesis of the disorders of cornification and the role of corneocyte proteins in these disorders An update on molecular aspects of the non-syndromic ichthyoses.Topical enzyme-replacement therapy restores transglutaminase 1 activity and corrects architecture of transglutaminase-1-deficient skin grafts.Transglutaminse 2 and EGGL, the protein cross-link formed by transglutaminse 2, as therapeutic targets for disabilities of old age.Matriptase-deficient mice exhibit ichthyotic skin with a selective shift in skin microbiota.Malignant skin tumours in patients with inherited ichthyosis.Epidermal barriers Activation of Molecular Signatures for Antimicrobial and Innate Defense Responses in Skin with Transglutaminase 1 Deficiency.Restoration of fatty aldehyde dehydrogenase deficiency in Sjögren-Larsson syndrome.Epidermal Notch1 loss promotes skin tumorigenesis by impacting the stromal microenvironment.Skin Barrier Development Depends on CGI-58 Protein Expression during Late-Stage Keratinocyte Differentiation.Tissue-specific responses to loss of transglutaminase 2.Akt-dependent Pp2a activity is required for epidermal barrier formation during late embryonic development.Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment.Stimulation of cell motility and expression of late markers of differentiation in human oral keratinocytes by Candida albicans.

P2860

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P2860

Development of ichthyosiform skin compensates for defective permeability barrier function in mice lacking transglutaminase 1

http://www.wikidata.org/entity/Q34786940

description

2002 nî lūn-bûn

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2002 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2002 թվականի հունվարին հրատարակված գիտական հոդված

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2002年の論文

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Development of ichthyosiform s ...... ice lacking transglutaminase 1

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Development of ichthyosiform s ...... ice lacking transglutaminase 1

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Development of ichthyosiform s ...... ice lacking transglutaminase 1

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Development of ichthyosiform s ...... ice lacking transglutaminase 1

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Development of ichthyosiform s ...... ice lacking transglutaminase 1

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Development of ichthyosiform s ...... ice lacking transglutaminase 1

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Development of ichthyosiform s ...... ice lacking transglutaminase 1

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P1433

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Journal of Clinical Investigation

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Development of ichthyosiform s ...... ice lacking transglutaminase 1

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Hiroyuki Morioka

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John M Robinson

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Kiyofumi Yamanishi

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Masato Matsuki

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Nobuo Kuramoto

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Takami Takizawa

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Toshihiro Takizawa

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P2860

Biochemical, structural, and transglutaminase substrate properties of human loricrin, the major epidermal cornified cell envelope protein

Isolation of a cDNA encoding a novel member of the transglutaminase gene family from human keratinocytes. Detection and identification of transglutaminase gene products based on reverse transcription-polymerase chain reaction with degenerate primers

Genotype/phenotype correlation in autosomal recessive lamellar ichthyosis

Two new loci for autosomal recessive ichthyosis on chromosomes 3p21 and 19p12-q12 and evidence for further genetic heterogeneity.

Transglutaminase 1 mutations in autosomal recessive congenital ichthyosis: private and recurrent mutations in an isolated population

Transglutaminase 5 cross-links loricrin, involucrin, and small proline-rich proteins in vitro

The complete amino acid sequence of the human transglutaminase K enzyme deduced from the nucleic acid sequences of cDNA clones

Ceramides are bound to structural proteins of the human foreskin epidermal cornified cell envelope

Mutations in the gene for transglutaminase 1 in autosomal recessive lamellar ichthyosis

Mutations of keratinocyte transglutaminase in lamellar ichthyosis

P304

243-250

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scholarly article

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10.1172/JCI0213563

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P433

2

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109

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2002-01-01T00:00:00Z

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11805136

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150837

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