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Aberrant nonfibrotic parenchyma in idiopathic pulmonary fibrosis is correlated with decreased β‐catenin inhibition and increased Wnt5a/b interaction
Idiopathic pulmonary fibrosis (IPF), an insidious disease with grave prognosis, is characterized by heterogeneous fibrosis with densely fibrotic areas surrounded by nonfibrotic normal‐looking tissue, believed to reflect a temporal development. The etiology is incompletely elucidated, but aberrant wo...
Autores principales: | Rydell‐Törmänen, Kristina, Zhou, Xiao‐Hong, Hallgren, Oskar, Einarsson, Jonas, Eriksson, Leif, Andersson‐Sjöland, Annika, Westergren‐Thorsson, Gunilla |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4823602/ https://www.ncbi.nlm.nih.gov/pubmed/26997628 http://dx.doi.org/10.14814/phy2.12727 |
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