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Description Figure 6. Most relevant molecular mechanisms and possible drugs for the treatment of EMT in pulmonary fibrosis.
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Source https://www.frontiersin.org/articles/10.3389/fcell.2020.607483/full The Epithelial-to-Mesenchymal Transition as a Possible Therapeutic Target in Fibrotic Disorders. Front. Cell Dev. Biol. 8:607483. doi: 10.3389/fcell.2020.607483
Author Di Gregorio J, Robuffo I, Spalletta S, Giambuzzi G, De Iuliis V, Toniato E, Martinotti S, Conti P and Flati V
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Copyright © 2020 Di Gregorio, Robuffo, Spalletta, Giambuzzi, De Iuliis, Toniato, Martinotti, Conti and Flati. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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current00:32, 19 May 2024Thumbnail for version as of 00:32, 19 May 20242,773 × 3,807 (381 KB)Rasbak (talk | contribs){{Information |description=Figure 6. Most relevant molecular mechanisms and possible drugs for the treatment of EMT in pulmonary fibrosis. |date=2020-12-21 |source=https://www.frontiersin.org/articles/10.3389/fcell.2020.607483/full The Epithelial-to-Mesenchymal Transition as a Possible Therapeutic Target in Fibrotic Disorders. Front. Cell Dev. Biol. 8:607483. doi: 10.3389/fcell.2020.607483 |author=Di Gregorio J, Robuffo I, Spalletta S, Giambuzzi G, De Iuliis V, Toniato E, Martinotti S, Conti...

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