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Article

A Desmoplakin Point Mutation with Enhanced Keratin Association Ameliorates Pemphigus Vulgaris Autoantibody-Mediated Loss of Cell Cohesion

8 Jul 2014

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Identifiers

PMID: 25010392
DOI: 10.1016/j.ajpath.2014.05.016

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Related research

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A Desmoplakin Point Mutation with Enhanced Keratin Association Ameliorates Pemphigus Vulgaris Autoantibody-Mediated Loss of Cell CohesionPMID 25010392Read ↗

Mechanisms Causing Loss of Keratinocyte Cohesion in PemphigusSemantic proximity Read ↗

Insights from a Desmoplakin Mutation Identified in Lethal Acantholytic Epidermolysis BullosaSemantic proximity Read ↗

Genetic diseases of junctions.Semantic proximity Read ↗

Molecular abnormalities of the desmosomal protein desmoplakin in human disease.Semantic proximity Read ↗

BPAG1-e restricts keratinocyte migration through control of adhesion stability.Semantic proximity Read ↗

Different signaling patterns contribute to loss of keratinocyte cohesion dependent on autoantibody profile in pemphigusSemantic proximity Read ↗

Keratins Regulate p38MAPK-Dependent Desmoglein Binding Properties in PemphigusSemantic proximity Read ↗

Clustering of desmosomal cadherins by desmoplakin is essential for cell-cell adhesionSemantic proximity Read ↗

Pemphigus-A Disease of Desmosome Dysfunction Caused by Multiple Mechanisms.Semantic proximity Read ↗

Analysis of the desmoplakin gene reveals striking conservation with other members of the plakin family of cytolinkers.Semantic proximity Read ↗

Loss of desmoplakin tail causes lethal acantholytic epidermolysis bullosa.Semantic proximity Read ↗

Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris.Semantic proximity Read ↗

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