Publisher Correction to: Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologies

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource, 1 online resource.

Language: Englisch

Bibliographic citation: Publisher Correction to: Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologies ; volume:11 ; number:1 ; day:12 ; month:7 ; year:2023 ; pages:1 ; date:12.2023
Acta Neuropathologica Communications ; 11, Heft 1 (12.7.2023), 1, 12.2023

Creator: Koga, Shunsuke
Murakami, Aya
Soto-Beasley, Alexandra I.
Walton, Ronald L.
Baker, Matthew C.
Castanedes-Casey, Monica
Josephs, Keith A.
Ross, Owen A.
Dickson, Dennis W.

Contributor: SpringerLink (Online service)

DOI: 10.1186/s40478-023-01621-x

URN: urn:nbn:de:101:1-2023101808375177094357

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:48 AM CEST

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Koga, Shunsuke
Murakami, Aya
Soto-Beasley, Alexandra I.
Walton, Ronald L.
Baker, Matthew C.
Castanedes-Casey, Monica
Josephs, Keith A.
Ross, Owen A.
Dickson, Dennis W.
SpringerLink (Online service)

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Publisher Correction to: Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologies

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Other Objects (12)

TDP-43 Pathology in Alzheimer’s Disease

Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologies

Molecular fragment characteristics and distribution of tangle associated TDP-43 (TATs) and other TDP-43 lesions in Alzheimer’s disease

C-terminal and full length TDP-43 specie differ according to FTLD-TDP lesion type but not genetic mutation

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Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologies

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C-terminal and full length TDP-43 specie differ according to FTLD-TDP lesion type but not genetic mutation

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Antibody against TDP-43 phosphorylated at serine 375 suggests conformational differences of TDP-43 aggregates among FTLD–TDP subtypes

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Molecular fragment characteristics and distribution of tangle associated TDP-43 (TATs) and other TDP-43 lesions in Alzheimer’s disease

C-terminal and full length TDP-43 specie differ according to FTLD-TDP lesion type but not genetic mutation

Disease‐linked TDP‐43 hyperphosphorylation suppresses TDP‐43 condensation and aggregation

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Antibody against TDP-43 phosphorylated at serine 375 suggests conformational differences of TDP-43 aggregates among FTLD–TDP subtypes

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