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- W1997809912 abstract "The identification of TDP-43 as the major component of the pathologic inclusions in most forms of sporadic and familial frontotemporal lobar degeneration with ubiquitin-positive inclusions (FTLD-U) and amyotrophic lateral sclerosis (ALS) resolved a long-standing enigma concerning the nature of the ubiquitinated disease protein under these conditions. Anti-TDP-43 immunohistochemistry and the recent development of novel tools, such as phosphorylation-specific TDP-43 antibodies, have increased our knowledge about the spectrum of pathological changes associated with FTLD-U and ALS and moreover, facilitated the neuropathological routine diagnosis of these conditions. This review summarizes the recent advances in our understanding on the molecular neuropathology and pathobiology of TDP-43 in FTLD and ALS." @default.
- W1997809912 created "2016-06-24" @default.
- W1997809912 creator A5062512325 @default.
- W1997809912 date "2009-01-09" @default.
- W1997809912 modified "2023-10-06" @default.
- W1997809912 title "Molecular Neuropathology of TDP-43 Proteinopathies" @default.
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- W1997809912 doi "https://doi.org/10.3390/ijms10010232" @default.
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