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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Main Authors: Has, Cristina, Herz, Corinna, Zimina, Elena, Qu, Hai-Yan, He, Yinghong, Zhang, Zhi-Gang, Wen, Ting-Ting, Gache, Yannick, Aumailley, Monique, Bruckner-Tuderman, Leena
Formato: Artigo
Idioma:Inglês
Publicado: American Society for Investigative Pathology 2009
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Regular Articles
Acceso en liña: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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