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Idiopathic pulmonary fibrosis is associated with tight junction protein alterations.
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Idiopathic pulmonary fibrosis is associated with tight junction protein alterations.
Idiopathic pulmonary fibrosis is associated with tight junction protein alterations. Biochim Biophys Acta Biomembr. 2020 05 01; 1862(5):183205.
View in:
PubMed
subject areas
Aged
Alveolar Epithelial Cells
Claudin-4
Claudins
Female
Humans
Idiopathic Pulmonary Fibrosis
Lung
Male
Middle Aged
Occludin
Respiratory Mucosa
Tight Junction Proteins
Tight Junctions
Zonula Occludens-1 Protein
authors with profiles
Christopher Weber
Le Shen