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Article

Cellular profiling identifies an early profibrotic alveolar type 2 cell signature in lung fibrosis

2025-05-23

Abstract excerpt

<h4>Rationale</h4> Idiopathic pulmonary fibrosis (IPF) is a progressive, age-associated, lung disease characterized by short telomeres in alveolar type 2 (AT2) cells, epithelial remodeling, and fibrosis. <h4>Objectives</h4> This study investigated how telomere dysfunction in AT2 cells lacking Telomere Repeat Binding Factor 1 (TRF1) drives lung remodeling in SPC-creTRF1 flox/flox mice and its relevance to IPF....

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Literature Corpus work
db856d59-875f-5fc5-88e7-b837acf9a1d0
DOI
10.1101/2025.05.22.655638
Open publication

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Cellular profiling identifies an early profibrotic alveolar type 2 cell signature in lung fibrosisDOI 10.1101/2025.05.22.655638
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