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Published in 2018 at "Cell reports"
DOI: 10.1016/j.celrep.2018.03.067
Abstract: SUMMARY Idiopathic pulmonary fibrosis (IPF) is characterized by aberrant accumulation of collagen-secreting myofibroblasts. Development of effective therapies is limited due to incomplete understanding of molecular mechanisms regulating myofibroblast expansion. FOXF1 transcription factor is expressed in…
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Keywords:
foxf1 inhibits;
inhibits pulmonary;
fibrosis;
cdh11 ... See more keywords