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. 2018 Aug 12;40(1):447–454. doi: 10.1080/0886022X.2018.1490322

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© 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 3. — Analysis of fibroblast-to-myofibroblast transition in vivo and in vitro. (A) Immunohistochemistry staining of α-SMA and vimentin (magnification, 200×) in the sham and the UUO models; (B) and (C) Semi-quantitative immunohistochemistry staining of α-SMA and vimentin in the sham group and the UUO model; (D) Immunofluorescence of α-SMA and vimentin in TGF-β1-activated fibroblast cell model. (E) and (F) IOD value of α-SMA and vimentin in the cell model. +p < .05 vs. the sham group, *p < .05 vs. UUO + the vehicle group, Δp < .05 vs. the control group, #p < .05 vs. the 5ng/ml TGF-β1 group; Arrow, positive signal.