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Published in 2021 at "JCI Insight"
DOI: 10.1172/jci.insight.141061
Abstract: Idiopathic pulmonary fibrosis (IPF) is characterized by aberrant repair that diminishes lung function via mechanisms that remain poorly understood. CC chemokine receptor (CCR10) and its ligand CCL28 were both elevated in IPF compared with normal…
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Keywords:
epha3 cells;
fibrosis;
fibrosis ipf;
ccr10 cells ... See more keywords