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J-GLOBAL ID:200902295842732729   Reference number:09A1058925

Regional distribution of TDP-43 inclusions in Alzheimer disease (AD) brains: Their relation to AD common pathology

アルツハイマー病(AD)脳におけるTDP-43抱合体の局部的分布:ADの一般病理との関係
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Volume: 29  Issue:Page: 566-573  Publication year: Oct. 2009 
JST Material Number: W0751A  ISSN: 0919-6544  Document type: Article
Article type: 原著論文  Country of issue: Australia (AUS)  Language: ENGLISH (EN)
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Basic neurology 
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Reference (29):
  • NEUMANN, M. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science. 2006, 314, 130-133
  • NEUMANN, M. TDP-43 Proteinopathy in frontotemporal lobar degeneration and amyotrophic lateral sclerosis : protein misfolding diseases without amyloidosis. Arch Neurol. 2007, 64, 1388-1394
  • KWONG, LK. TDP-43 proteinopathy : the neuropathology underlying major forms of sporadic and familial frontotemporal lobar degeneration and motor neuron disease. Acta Neuropathol. 2007, 114, 63-70
  • CAIRNS, NJ. TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions. Am J Pathol. 2007, 171, 227-240
  • MACKENZIE, IR. Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations. Ann Neurol. 2007, 61, 427-434
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