Progeria—a Rare Genetic Condition with Accelerated Ageing Process
Author:
Publisher
Springer Science and Business Media LLC
Subject
Molecular Biology,Applied Microbiology and Biotechnology,Biochemistry,General Medicine,Bioengineering,Biotechnology
Link
https://link.springer.com/content/pdf/10.1007/s12010-021-03514-y.pdf
Reference50 articles.
1. Carvalho, V. O., Celli, A., BanckeLaverde, B. L., Cunico, C., Santos Piedade, G., Lucas de Mello, M., & Beirao Junior, P. S. (2016). Progeria and the early aging in children: a case report. Dermatology Online Journal, 22(2), 13030/qt7kt4f85m.
2. Piekarowicz, et al. (2019). Hutchinson-Gilford progeria syndrome—current status and prospects for gene therapy treatment. Cells, 8(2), 88. https://doi.org/10.3390/cells8020088.
3. Harhouri, et al. (2018). An overview of treatment strategies for Hutchinson-Gilford Progeria syndrome. Nucleus., 9(1), 246–257. https://doi.org/10.1080/19491034.2018.1460045.
4. Santiago-Fernández, et al. (2019). Development of a CRISPR/Cas9-based therapy for Hutchinson-Gilford progeria syndrome. Nature Medicine, 25(3), 423–426. https://doi.org/10.1038/s41591-018-0338-6.
5. Zhang, J., Lian, Q., Zhu, G., Zhou, F., Sui, L., Tan, C., Mutalif, R. A., Navasankari, R., Zhang, Y., Tse, H. F., Stewart, C. L., & Colman, A. (2011). A human iPSC model of Hutchinson-Gilford progeria reveals vascular smooth muscle and mesenchymal stem cell defects. Cell Stem Cell, 8, 31–45.
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