TDP-43 proteinopathy: the neuropathology underlying major forms of sporadic and familial frontotemporal lobar degeneration and motor neuron disease

By Kwong Linda   Neumann Manuela   Sampathu Deepak   Lee Virginia   Trojanowski John  

Acta Neuropathologica, Vol. 114, Iss. 1, 2007-07 ,pp. : 63-70

Springer Publishing Company

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Phosphorylated TDP-43 in Alzheimer's disease and dementia with Lewy bodies

By Arai Tetsuaki  

Acta Neuropathologica, Vol. 117, Iss. 2, 2009-02 ,pp. : 125-136

Springer Publishing Company

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TDP-43 plasma levels do not differentiate sporadic inclusion body myositis from other inflammatory myopathies

By Kuiperij H.   Abdo Wilson   Engelen Baziel   Schelhaas H.   Verbeek Marcel  

Acta Neuropathologica, Vol. 120, Iss. 6, 2010-12 ,pp. : 825-826

Springer Publishing Company

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Sporadic amyotrophic lateral sclerosis of long duration is associated with relatively mild TDP-43 pathology

By Nishihira Yasushi   Tan Chun-Feng   Hoshi Yasuhiro   Iwanaga Keisuke   Yamada Megumi   Kawachi Izumi   Tsujihata Mitsuhiro   Hozumi Isao   Morita Takashi   Onodera Osamu   Nishizawa Masatoyo   Kakita Akiyoshi   Takahashi Hitoshi  

Acta Neuropathologica, Vol. 117, Iss. 1, 2009-01 ,pp. : 45-53

Springer Publishing Company

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TDP-43 Dimerizes in Human Cells in Culture

By Shiina Yuki   Arima Kunimasa   Tabunoki Hiroko   Satoh Jun-ichi  

Cellular and Molecular Neurobiology, Vol. 30, Iss. 4, 2010-05 ,pp. : 641-652

Springer Publishing Company

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