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Kindlin-1 Regulates Integrin Dynamics and Adhesion Turnover
Loss-of-function mutations in the gene encoding the integrin co-activator kindlin-1 cause Kindler syndrome. We report a novel kindlin-1-deficient keratinocyte cell line derived from a Kindler syndrome patient. Despite the expression of kindlin-2, the patient’s cells display several hallmarks related...
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| Hauptverfasser: | , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Public Library of Science
2013
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3679067/ https://ncbi.nlm.nih.gov/pubmed/23776470 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0065341 |
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