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Epidermal deletion of Kindlin-1 drives matrix changes in the mouse skin and altered responses to ultraviolet radiation
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DOI：10.1016/j.jdermsci.2026.04.007.png)
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Abstract
En 中文
Kindler syndrome (KS) or Kindler epidermolysis bullosa (KEB) is a rare genetic autosomal skin fragility disorder with photosensitivity and abnormal pigmentation, with patients also having an increased risk of developing cutaneous squamous cell carcinoma (cSCC).
Keywords:
Kindler syndrome
Kindler epidermolysis bullosa
epithelial-to-mesenchymal transition
UV radiation
antioxidant
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