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. 2019 Oct 17;10:4723. doi: 10.1038/s41467-019-12664-x

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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. 5 — Hyper-long telomere mice show longer telomeres throughout their lifespan in both proliferative and non-proliferative tissues. a–f Mean telomere fluorescence and percentage of short telomeres in back skin (a, b), intestine (c, d), brain (e, f) in 100 weeks-old hyper-long telomere mice and age-matched controls. Error bars represent standard error. t-test was used for statistical analysis. The number of mice is indicated in each case. *p < 0.05. **p < 0.01. ***p < 0.001. Source data are provided as a Source Data file