Significance and limitation of the pathological classification of TDP-43 proteinopathy
Author:
Affiliation:
1. Department of Neuropsychiatry, Division of Clinical Medicine, Faculty of Medicine; University of Tsukuba; Tsukuba Japan
2. Department of Dementia and Higher Brain Function; Tokyo Metropolitan Institute of Medical Science; Tokyo Japan
Publisher
Wiley
Subject
Neurology (clinical),General Medicine,Pathology and Forensic Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/neup.12138/fullpdf
Reference108 articles.
1. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis;Neumann;Science,2006
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. Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43;Davidson;Acta Neuropathol (Berl),2007
4. TDP-43 proteinopathy in frontotemporal lobar degeneration and amyotrophic lateral sclerosis: protein misfolding diseases without amyloidosis;Neumann;Arch Neurol,2007
5. Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations;Mackenzie;Ann Neurol,2007
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