Kindlin-1 Regulates Epidermal Growth Factor Receptor Signaling

Kindler syndrome is an autosomal recessive genodermatosis that results from mutations in the FERMT1 gene encoding t kindlin-1. Kindlin-1 localizes to focal adhesion and is known to contribute to the activation of integrin receptors. Most cases of Kindler syndrome show a reduction or complete absence...

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發表在:J Invest Dermatol
Main Authors: Michael, Magdalene, Begum, Rumena, Chan, Grace K., Whitewood, Austin J., Matthews, Daniel R., Goult, Benjamin T., McGrath, John A., Parsons, Maddy
格式: Artigo
語言:Inglês
出版: Elsevier 2019
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Article
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC6345584/
https://ncbi.nlm.nih.gov/pubmed/30248333
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jid.2018.08.020
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