Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD-Reference-Cited by-同舟云学术

Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD

Published:2016-02-12 Issue:1 Volume:6 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Boeynaems Steven,Bogaert Elke,Michiels Emiel,Gijselinck Ilse,Sieben Anne,Jovičić Ana,De Baets Greet,Scheveneels Wendy,Steyaert Jolien,Cuijt Ivy,Verstrepen Kevin J.,Callaerts Patrick,Rousseau Frederic,Schymkowitz Joost,Cruts Marc,Van Broeckhoven Christine,Van Damme Philip,Gitler Aaron D.,Robberecht Wim,Van Den Bosch Ludo

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep20877.pdf

Reference30 articles.

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2. DeJesus-Hernandez, M. et al. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 72, 245–256 (2011).

3. Ling, S. C., Polymenidou, M. & Cleveland, D. W. Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis. Neuron 79, 416–438 (2013).

4. Mori, K. et al. The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS. Science 339, 1335–1338 (2013).

5. Zu, T. et al. RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementia. Proceedings of the National Academy of Sciences of the United States of America 110, E4968–4977 (2013).

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