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Modeling Idiopathic Pulmonary Fibrosis in Humanized Severe Combined Immunodeficient Mice

Idiopathic pulmonary fibrosis (IPF) is a fibrotic lung disease of unknown etiopathogenesis with limited therapeutic options. IPF is characterized by an abundance of fibroblasts and loss of epithelial progenitors, which cumulates in unrelenting fibrotic lung remodeling and loss of normal oxygenation....

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Detalhes bibliográficos
Publicado no:Am J Pathol
Main Authors: Habiel, David M., Espindola, Milena S., Coelho, Ana L., Hogaboam, Cory M.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Investigative Pathology 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5954978/
https://ncbi.nlm.nih.gov/pubmed/29378172
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajpath.2017.12.020
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