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Journal of Ophthalmology
Volume 2015, Article ID 579695, 8 pages
Research Article

Epigenetic Regulation of Werner Syndrome Gene in Age-Related Cataract

Eye Institute, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226001, China

Received 31 December 2014; Revised 11 March 2015; Accepted 13 March 2015

Academic Editor: Jun Zhang

Copyright © 2015 Xi Zhu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Citations to this Article [8 citations]

The following is the list of published articles that have cited the current article.

  • Hoi-Hung Cheung, Duanqing Pei, and Wai-Yee Chan, “Stem cell aging in adult progeria,” Cell Regeneration, vol. 4, no. 1, 2015. View at Publisher · View at Google Scholar
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  • Yong Wang, and Huaijin Guan, “The Role of DNA Methylation in Lens Development and Cataract Formation,” Cellular and Molecular Neurobiology, 2016. View at Publisher · View at Google Scholar
  • Raghavendra A. Shamanna, Deborah L. Croteau, Jong-Hyuk Lee, and Vilhelm A. Bohr, “Recent Advances in Understanding Werner Syndrome,” F1000Research, vol. 6, pp. 1779, 2017. View at Publisher · View at Google Scholar
  • Huaijin Guan, and Yong Wang, “Research progress of DNA methylation in lens development and cataract,” Zhonghua Shiyan Yanke Zazhi/Chinese Journal of Experimental Ophthalmology, vol. 35, no. 8, pp. 747–751, 2017. View at Publisher · View at Google Scholar
  • Bondanini, Bacalini, Gentilini, Pisoni, Raimondo, Guastafierro, Spanò, Garagnani, Marcoccia, Di Blasio, Corsi, and Franceschi, “Genome-wide DNA methylation analysis in blood cells from patients with Werner syndrome,” Clinical Epigenetics, vol. 9, no. 1, 2017. View at Publisher · View at Google Scholar
  • Tiziana Guastafierro, Maria Giulia Bacalini, Antonella Marcoccia, Alberto Spanò, Domenico Raimondo, Claudio Franceschi, and Francesco Bondanini, “Shaping the epigenetic basis of Werner Syndrome,” Biochimica Clinica, vol. 42, no. 3, pp. 210–216, 2018. View at Publisher · View at Google Scholar
  • Sofie Lautrup, Domenica Caponio, Hoi-Hung Cheung, Claudia Piccoli, Tinna Stevnsner, Wai-Yee Chan, and Evandro F. Fang, “Studying Werner syndrome to elucidate mechanisms and therapeutics of human aging and age-related diseases,” Biogerontology, 2019. View at Publisher · View at Google Scholar