Modeling xeroderma pigmentosum associated neurological pathologies with patients-derived iPSCs-Reference-Cited by-同舟云学术

Modeling xeroderma pigmentosum associated neurological pathologies with patients-derived iPSCs

Published:2016-02-13 Issue:3 Volume:7 Page:210-221
ISSN:1674-800X
Container-title:Protein & Cell
language:en
Short-container-title:Protein Cell

Author:

Fu Lina,Xu Xiuling,Ren Ruotong,Wu Jun,Zhang Weiqi,Yang Jiping,Ren Xiaoqing,Wang Si,Zhao Yang,Sun Liang,Yu Yang,Wang Zhaoxia,Yang Ze,Yuan Yun,Qiao Jie,Belmonte Juan Carlos Izpisua,Qu Jing,Liu Guang-Hui

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Drug Discovery,Biochemistry,Biotechnology

Link

http://link.springer.com/content/pdf/10.1007/s13238-016-0244-y.pdf

Reference39 articles.

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2. Andressoo JO et al (2009) An Xpb mouse model for combined Xeroderma pigmentosum and cockayne syndrome reveals progeroid features upon further attenuation of DNA repair. Mol Cell Biol 29(5):1276–1290

3. Anttinen A et al (2008) Neurological symptoms and natural course of xeroderma pigmentosum. Brain 131:1979–1989

4. Cattoglio C et al (2015) Functional and mechanistic studies of XPC DNA-repair complex as transcriptional coactivator in embryonic stem cells. Proc Natl Acad Sci U S A 112(18):E2317–E2326

5. Cheung HH et al (2014) Telomerase protects werner syndrome lineage-specific stem cells from premature aging. Stem Cell Reports 2(4):534–546

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