TDP-43 associates with stalled ribosomes and contributes to cell survival during cellular stress
Article first published online: 1 MAR 2013
© 2013 International Society for Neurochemistry
Journal of Neurochemistry
Volume 126, Issue 2, pages 288–300, July 2013
How to Cite
J. Neurochem.(2013)126, 288–300.
- Issue published online: 2 JUL 2013
- Article first published online: 1 MAR 2013
- Accepted manuscript online: 8 FEB 2013 10:42AM EST
- Manuscript Accepted: 6 FEB 2013
- Manuscript Revised: 5 FEB 2013
- Manuscript Received: 23 AUG 2012
- Kurata Memorial Hitachi Science and Technology Foundation
- Grants-in-Aid for Young Scientist. Grant Number: 23791008
- Grants-in-Aid for Scientific Research
- Strategic Research Program for Brain Sciences
- Ministry of Education, Culture, Sports, Science
- Grants-in-Aid for Scientific Research from the Ministry of Health, Labour and Welfare. Grant Numbers: 10102894, 10103470
- the Ministry of Education, Culture, Science. Grant Number: 09019658
- Japan Science and Technology Agency
Figure S1. (a–d) Cell extracts obtained from HeLa cells treated with 0.5 mM ARS for 1 h (a).
Figure S2. (a) The domain architectures of wild-type (WT) TDP-43 or TDP-43 bearing mutation of serines (Ser403/404/409/410) to alanines (Ala) are shown schematically.
Figure S3. SH-SY5Y neuronal cells were untreated (Control) or treated with 0.25 mM ARS for 0.5 h, and then analyzed by fluorescence in situ hybridization, as indicated.
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