FUS pathology in basophilic inclusion body disease-Reference-Cited by-同舟云学术

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FUS pathology in basophilic inclusion body disease

Published:2009-10-15 Issue:5 Volume:118 Page:617-627
ISSN:0001-6322
Container-title:Acta Neuropathologica
language:en
Short-container-title:Acta Neuropathol

Author:

Munoz David G.,Neumann Manuela,Kusaka Hirofumi,Yokota Osamu,Ishihara Kenji,Terada Seishi,Kuroda Shigetoshi,Mackenzie Ian R.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00401-009-0598-9.pdf

Reference66 articles.

1. Aizawa H, Kimura T, Hashimoto K et al (2000) Basophilic cytoplasmic inclusions in a case of sporadic juvenile amyotrophic lateral sclerosis. J Neurol Sci 176:109–113

2. Aman P, Panagopoulos I, Lassen C et al (1996) Expression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUS. Genomics 37:1–8

3. Andersson MK, Stahlberg A, Arvidsson Y et al (2008) The multifunctional FUS, EWS and TAF15 proto-oncoproteins show cell type-specific expression patterns and involvement in cell spreading and stress response. BMC Cell Biol 9:37

4. Arai T, Hasegawa M, Akiyama H et al (2006) TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Biochem Biophys Res Commun 351:602–611

5. Baechtold H, Kuroda M, Sok J et al (1999) Human 75-kDa DNA-pairing protein is identical to the pro-oncoprotein TLS/FUS and is able to promote D-loop formation. J Biol Chem 274:34337–34342

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