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...

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Detalles Bibliográficos
Autores principales: Rydell‐Törmänen, Kristina, Zhou, Xiao‐Hong, Hallgren, Oskar, Einarsson, Jonas, Eriksson, Leif, Andersson‐Sjöland, Annika, Westergren‐Thorsson, Gunilla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Original Research
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

Internet

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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