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Kindlin-1 Is Required for RhoGTPase-Mediated Lamellipodia Formation in Keratinocytes
Kindlin-1 is an epithelial-specific member of the novel kindlin protein family, which are regulators of integrin functions. Mutations in the gene that encodes Kindlin-1, FERMT1 (KIND1), cause the Kindler syndrome (KS), a human disorder characterized by mucocutaneous fragility, progressive skin atrop...
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| Päätekijät: | , , , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
American Society for Investigative Pathology
2009
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2751541/ https://ncbi.nlm.nih.gov/pubmed/19762715 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/ajpath.2009.090203 |
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