Glycogen Synthase Kinase-3β Inhibition with 9-ING-41 Attenuates the Progression of Pulmonary Fibrosis

Idiopathic pulmonary fibrosis (IPF) is a progressive interstitial lung disease with a median survival of 3 years after diagnosis. Although the etiology of IPF is unknown, it is characterized by extensive alveolar epithelial cell apoptosis and proliferation of myofibroblasts in the lungs. While the o...

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Detalles Bibliográficos
Autores principales: Jeffers, Ann, Qin, Wenyi, Owens, Shuzi, Koenig, Kathleen B., Komatsu, Satoshi, Giles, Francis J., Schmitt, Daniel M., Idell, Steven, Tucker, Torry A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908609/
https://www.ncbi.nlm.nih.gov/pubmed/31831767
http://dx.doi.org/10.1038/s41598-019-55176-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908609/
https://www.ncbi.nlm.nih.gov/pubmed/31831767
http://dx.doi.org/10.1038/s41598-019-55176-w

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