Molecular analysis and biochemical classification of TDP-43 proteinopathy-Reference-Cited by-同舟云学术

Molecular analysis and biochemical classification of TDP-43 proteinopathy

Published:2012-10-03 Issue:11 Volume:135 Page:3380-3391
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Tsuji Hiroshi,Arai Tetsuaki,Kametani Fuyuki,Nonaka Takashi,Yamashita Makiko,Suzukake Masami,Hosokawa Masato,Yoshida Mari,Hatsuta Hiroyuki,Takao Masaki,Saito Yuko,Murayama Shigeo,Akiyama Haruhiko,Hasegawa Masato,Mann David M. A.,Tamaoka Akira

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/135/11/3380/17346806/aws230.pdf

Reference40 articles.

1. Phosphorylated TDP-43 in Alzheimer's disease and dementia with Lewy bodies;Arai;Acta Neuropathol (Berl),2009

2. TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis;Arai;Biochem Biophys Res Commun,2006

3. Identification of amino-terminally cleaved tau fragments that distinguish progressive supranuclear palsy from corticobasal degeneration;Arai;Ann Neurol,2004

4. Neuropathological heterogeneity in frontotemporal lobar degeneration with TDP-43 proteinopathy: a quantitative study of 94 cases using principal components analysis;Armstrong;J Neural Transm,2010

5. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17;Baker;Nature,2006

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