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Biochemical classification of tauopathies by immunoblot, protein sequence and mass spectrometric analyses of sarkosyl-insoluble and trypsin-resistant tau.
Taniguchi-Watanabe S, Arai T, Kametani F, Nonaka T, Masuda-Suzukake M, Tarutani A, Murayama S, Saito Y, Arima K, Yoshida M, Akiyama H, Robinson A, Mann DMA, Iwatsubo T, Hasegawa M. Taniguchi-Watanabe S, et al. Among authors: yoshida m. Acta Neuropathol. 2016 Feb;131(2):267-280. doi: 10.1007/s00401-015-1503-3. Epub 2015 Nov 4. Acta Neuropathol. 2016. PMID: 26538150 Free PMC article.
Clinical and neuropathological correlates of Lewy body disease.
Hishikawa N, Hashizume Y, Yoshida M, Sobue G. Hishikawa N, et al. Among authors: yoshida m. Acta Neuropathol. 2003 Apr;105(4):341-50. doi: 10.1007/s00401-002-0651-4. Epub 2003 Jan 14. Acta Neuropathol. 2003. PMID: 12624787
Tuft-shaped astrocytes in Lewy body disease.
Hishikawa N, Hashizume Y, Yoshida M, Niwa J, Tanaka F, Sobue G. Hishikawa N, et al. Among authors: yoshida m. Acta Neuropathol. 2005 Apr;109(4):373-80. doi: 10.1007/s00401-004-0967-3. Epub 2005 Jan 25. Acta Neuropathol. 2005. PMID: 15668789
An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains.
Ishikawa K, Toru S, Tsunemi T, Li M, Kobayashi K, Yokota T, Amino T, Owada K, Fujigasaki H, Sakamoto M, Tomimitsu H, Takashima M, Kumagai J, Noguchi Y, Kawashima Y, Ohkoshi N, Ishida G, Gomyoda M, Yoshida M, Hashizume Y, Saito Y, Murayama S, Yamanouchi H, Mizutani T, Kondo I, Toda T, Mizusawa H. Ishikawa K, et al. Among authors: yoshida m. Am J Hum Genet. 2005 Aug;77(2):280-96. doi: 10.1086/432518. Epub 2005 Jul 6. Am J Hum Genet. 2005. PMID: 16001362 Free PMC article.
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