Identification of telomere dysfunction in Friedreich ataxia-Reference-Cited by-同舟云学术

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Identification of telomere dysfunction in Friedreich ataxia

Published:2015-06-10 Issue:1 Volume:10 Page:
ISSN:1750-1326
Container-title:Molecular Neurodegeneration
language:en
Short-container-title:Mol Neurodegeneration

Author:

Anjomani Virmouni Sara,Al-Mahdawi Sahar,Sandi Chiranjeevi,Yasaei Hemad,Giunti Paola,Slijepcevic Predrag,Pook Mark A.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Molecular Biology

Link

http://link.springer.com/content/pdf/10.1186/s13024-015-0019-6.pdf

Reference51 articles.

1. Chamberlain S, Lewis PD. Studies of cellular hypersensitivity to ionising radiation in Friedreich’s ataxia. J Neurol Neurosurg Psychiatry. 1982;45:1136–8.

2. Haugen AC, Di Prospero NA, Parker JS, Fannin RD, Chou J, Meyer JN, et al. Altered gene expression and DNA damage in peripheral blood cells from Friedreich’s ataxia patients: cellular model of pathology. PLoS Genet. 2010;6:e1000812.

3. Coppola G, Burnett R, Perlman S, Versano R, Gao F, Plasterer H, et al. A gene expression phenotype in lymphocytes from Friedreich ataxia patients. Ann Neurol. 2011;70:790–804.

4. von Zglinicki T. Oxidative stress shortens telomeres. Trends Biochem Sci. 2002;27:339–44.

5. Castaldo I, Vergara P, Pinelli M, Filla A, De Michele G, Cocozza S, et al. Can telomere shortening in human peripheral blood leukocytes serve as a disease biomarker of Friedreich’s ataxia? Antioxid Redox Signal. 2013;18:1303–6.

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