Reactome | Epidermolysis bullosa simplex (Dowling-Meara type) is a genetic disease characterized by an abnormal keratin-filament network involving keratins K5 and K14

Epidermolysis bullosa simplex (Dowling-Meara type) is a genetic disease characterized by an abnormal keratin-filament network involving keratins K5 and K14 Show undefined attributes

cell

[Cell:R-HSA-9725625] transit-amplifying cell of epidermis basal layer - Homo sapiens

created [InstanceEdit:9725578] Orlic-Milacic, Marija, 2021年03月29日

dbId 9725601

displayName Epidermolysis bullosa simplex (Dowling-Meara type) is a genetic disease characterized by an abnormal keratin-filament network involving keratins K5 and K14

literatureReference

[LiteratureReference:9725561] Epidermolysis bullosa simplex (Dowling-Meara type) is a genetic disease characterized by an abnormal keratin-filament network involving keratins K5 and K14
[LiteratureReference:9725598] Human embryonic stem-cell derivatives for full reconstruction of the pluristratified epidermis: a preclinical study
[LiteratureReference:9725607] K15 expression implies lateral differentiation within stratified epithelial basal cells
[LiteratureReference:9725585] Keratinocyte Differentiation by Flow Cytometry
[LiteratureReference:9725620] Localisation of keratin K78 in the basal layer and first suprabasal layers of stratified epithelia completes expression catalogue of type II keratins and provides new insights into sequential keratin expression
[LiteratureReference:9820674] CellMarker 2.0: an updated database of manually curated cell markers in human/mouse and web tools based on scRNA-seq data
[LiteratureReference:9839484] PanglaoDB: a web server for exploration of mouse and human single-cell RNA sequencing data

marker [EntityWithAccessionedSequence:R-HSA-446091] KRT14 [cytosol]

modified [InstanceEdit:9839715] Orlic-Milacic, Marija, 2023年07月07日

schemaClass MarkerReference

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(markerReference)

[Cell:R-HSA-9725625] transit-amplifying cell of epidermis basal layer

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Reactome Pathway Database

Epidermolysis bullosa simplex (Dowling-Meara type) is a genetic disease characterized by an abnormal keratin-filament network involving keratins K5 and K14 Show undefined attributes

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