Striate palmoplantar keratoderma arising from desmoplakin and desmoglein 1 mutations is associated with contrasting perturbations of desmosomes and the keratin filament network. - Wikidata - wikimedia - TriplyDB

Striate palmoplantar keratoderma arising from desmoplakin and desmoglein 1 mutations is associated with contrasting perturbations of desmosomes and the keratin filament network.

Striate palmoplantar keratoderma arising from desmoplakin and desmoglein 1 mutations is associated with contrasting perturbations of desmosomes and the keratin filament network.

http://www.wikidata.org/entity/Q47588181

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Perturbed desmosomal cadherin expression in grainy head-like 1-null mice Cytoskeleton in motion: the dynamics of keratin intermediate filaments in epithelia Involvement of corneodesmosome degradation and lamellar granule transportation in the desquamation process Cadherins as targets for genetic diseases.Nuclear staining and relative distance for quantifying epidermal differentiation in biomarker expression profiling.Plakoglobin rescues adhesive defects induced by ectodomain truncation of the desmosomal cadherin desmoglein 1: implications for exfoliative toxin-mediated skin blistering.MMP-9 and CXCL8/IL-8 are potential therapeutic targets in epidermolysis bullosa simplex.microRNA-31/factor-inhibiting hypoxia-inducible factor 1 nexus regulates keratinocyte differentiation The desmosome and pemphigus.Desmoglein-1/Erbin interaction suppresses ERK activation to support epidermal differentiation.Desmoglein-1, differentiation, and disease.Diseases of epidermal keratins and their linker proteins Desmoglein 1-dependent suppression of EGFR signaling promotes epidermal differentiation and morphogenesis Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma.Hepatocyte growth factor activator inhibitor type 1 maintains the assembly of keratin into desmosomes in keratinocytes by regulating protease-activated receptor 2-dependent p38 signaling.Desmosomes and Intermediate Filaments: Their Consequences for Tissue Mechanics.Mimickers of classic acantholytic diseases.The requirement for perp in postnatal viability and epithelial integrity reflects an intrinsic role in stratified epithelia.Deregulation of keratinocyte differentiation and activation: a hallmark of venous ulcers Cardiac autoantibodies from patients affected by a new variant of endemic pemphigus foliaceus in Colombia, South America.Striate palmar keratoderma and antiretroviral treatment for human immunodeficiency virus infection: not just a coincidence.Cell autonomous role of iASPP deficiency in causing cardiocutaneous disorders.Disorders of Keratinization

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P2860

Striate palmoplantar keratoderma arising from desmoplakin and desmoglein 1 mutations is associated with contrasting perturbations of desmosomes and the keratin filament network.

http://www.wikidata.org/entity/Q47588181

description

2004 nî lūn-bûn

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2004年の論文

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年學術文章

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Striate palmoplantar keratoder ...... the keratin filament network.

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Striate palmoplantar keratoder ...... the keratin filament network.

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Striate palmoplantar keratoder ...... the keratin filament network.

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Striate palmoplantar keratoder ...... the keratin filament network.

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Striate palmoplantar keratoder ...... the keratin filament network.

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Striate palmoplantar keratoder ...... the keratin filament network.

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J.1365-2133.2004.05996.X

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British Journal of Dermatology

P1476

Striate palmoplantar keratoder ...... the keratin filament network.

@en

P2093

Armstrong DK

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Buxton RS

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Dopping-Hepenstal PJ

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Eady RA

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South AP

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Stone MG

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P2860

Haploinsufficiency of desmoplakin causes a striate subtype of palmoplantar keratoderma

Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome

Suprabasal desmoglein 3 expression in the epidermis of transgenic mice results in hyperproliferation and abnormal differentiation.

Breaking the connection: displacement of the desmosomal plaque protein desmoplakin from cell-cell interfaces disrupts anchorage of intermediate filament bundles and alters intercellular junction assembly

Increased expression of keratin 16 causes anomalies in cytoarchitecture and keratinization in transgenic mouse skin

The amino-terminal domain of desmoplakin binds to plakoglobin and clusters desmosomal cadherin-plakoglobin complexes

Striate palmoplantar keratoderma resulting from desmoplakin haploinsufficiency

Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma

Genomic amplification of the human plakophilin 1 gene and detection of a new mutation in ectodermal dysplasia/skin fragility syndrome

Desmosomal cadherins

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