Keratinocytes from Patients Lacking Collagen XVII Display a Migratory Phenotype

Acquired or inherited junctional epidermolysis bullosa are skin diseases characterized by a separation between the epidermis and the dermis. In inherited nonlethal junctional epidermolysis bullosa, genetic analysis has identified mutations in the COL17A1 gene coding for the transmembrane collagen XV...

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Bibliographic Details
Main Authors: Tasanen, Kaisa, Tunggal, Lucy, Chometon, Gretel, Bruckner-Tuderman, Leena, Aumailley, Monique
Format: Artigo
Language:Inglês
Published: American Society for Investigative Pathology 2004
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Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1615787/
https://ncbi.nlm.nih.gov/pubmed/15161638
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