Amyotrophic lateral sclerosis models and human neuropathology: similarities and differences
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Clinical Neurology,Pathology and Forensic Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00401-007-0308-4.pdf
Reference103 articles.
1. Aoki M (2004) Amyotrophic lateral sclerosis: recent insights from transgenic animal models with SOD1 mutations. Rinsho Shinkeigaku 44:778–791
2. Aoki M, Kato S, Nagai M, Itoyama Y (2005) Development of a rat model of amyotrophic lateral sclerosis expressing a human SOD1 transgene. Neuropathology 25:365–370
3. Arai T, Hasegawa M, Akiyama H, Ikeda K, Nonaka T, Mori H, Mann D, Tsuchiya K, Yoshida M, Hashizume Y, Oda T (2006) TDP-43 is a component of ubiquitin-positive inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Biochem Biophys Res Commun 351:602–611
4. Beaulieu JM, Nguyen MD, Julien JP (1999) Late onset death of motor neurons in mice over-expressing wild-type peripherin. J Cell Biol 147:531–544
5. Beaulieu JM, Jacomy H, Julien JP (2000) Formation of intermediate filament protein aggregates with disparate effects in two transgenic mouse models lacking the neurofilament light subunit. J Neurosci 20:5321–5328
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