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. 2019 Jan 25;10(2):63. doi: 10.1038/s41419-018-0951-9

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© The Author(s) 2019

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 4 — a Immunofluorescence analysis of primary cilia in molar section (red arrow). Primary cilia were stained with acetylated α-tubulin (green) antibody. DAPI is used as a counterstain. Scale bars represent 50 μm. b Calculated cilia percentage (n = 3 with at least 100 cells analyzed) is shown in a. c Calculated cilia length (n = 20 cells). Data are expressed as mean ± SEM; ns, not statistically significant; ***p < 0.0001