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Early-stage idiopathic pulmonary fibrosis is characterized by bronchoalveolar accumulation of SPP1 <sup>+</sup> macrophages

2023-12-08

Abstract excerpt

Patients affected by idiopathic pulmonary fibrosis (IPF), a progressive chronic and eventually fatal lung disease with unknown cause, suffer from delayed diagnosis and limited personalized treatment options due to the lack of predictive and staging relevant disease markers. Prior studies focused on the cellular and transcriptomic changes found in lung tissue during terminal IPF-associated lung fibrosis. In clinica...

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Literature Corpus work
10eca9e7-26d1-5414-8e27-ece284169156
DOI
10.1101/2023.12.06.569201
Open publication

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Early-stage idiopathic pulmonary fibrosis is characterized by bronchoalveolar accumulation of SPP1 <sup>+</sup> macrophagesDOI 10.1101/2023.12.06.569201
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