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首页> 外文期刊>Drug discovery today. Disease models >Hereditary bullous diseases: current and innovative models to study the skin blistering disease epidermolysis bullosa
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Hereditary bullous diseases: current and innovative models to study the skin blistering disease epidermolysis bullosa

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As the largest organ of the human body, our skin serves as an interface to the environment, as well as a defensive barrier against dangers therein. Its integrity is facilitated by a complex suprastructural network of proteins that tether the epidermis to the underlying dermis. Mutations in single genes that disrupt the function of these proteins lead to severe bullous disorders such as epidermolysis bullosa (EB). This short review focuses on progress in the establishment of different model systems that recapitulate multiple aspects of the pathological pheno-type of EB. These models have been used to decipher disease modifying mechanisms and evaluate therapeutic possibilities aimed at reverting the genetic defect or ameliorating disease-associated complications.

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