WISP1 mediates IL-6-dependent proliferation in primary human lung fibroblasts

Idiopathic pulmonary fibrosis (IPF) is a progressive and fatal interstitial lung disease. IPF is characterized by epithelial cell injury and reprogramming, increases in (myo)fibroblasts, and altered deposition of extracellular matrix. The Wnt1-inducible signaling protein 1 (WISP1) is involved in imp...

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Detalles Bibliográficos
Autores principales: Klee, S., Lehmann, M., Wagner, D. E., Baarsma, H. A., Königshoff, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751539/
https://www.ncbi.nlm.nih.gov/pubmed/26867691
http://dx.doi.org/10.1038/srep20547

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751539/
https://www.ncbi.nlm.nih.gov/pubmed/26867691
http://dx.doi.org/10.1038/srep20547

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