Evidence of cerebellar TDP-43 loss of function in FTLD-TDP

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2051-5960

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Evidence of cerebellar TDP-43 loss of function in FTLD-TDP ; volume:10 ; number:1 ; day:25 ; month:7 ; year:2022 ; pages:1-9 ; date:12.2022
Acta Neuropathologica Communications ; 10, Heft 1 (25.7.2022), 1-9, 12.2022

Creator: Pickles, Sarah
Gendron, Tania F.
Koike, Yuka
Yue, Mei
Song, Yuping
Kachergus, Jennifer M.
Shi, J.
DeTure, Michael
Thompson, E. Aubrey
Oskarsson, Björn
Graff-Radford, Neill R.
Boeve, Bradley F.
Petersen, Ronald C.
Wszolek, Zbigniew K.
Josephs, Keith A.
Dickson, Dennis W.
Petrucelli, Leonard
Cook, Casey N.
Prudencio, Mercedes

Contributor: SpringerLink (Online service)

DOI: 10.1186/s40478-022-01408-6

URN: urn:nbn:de:101:1-2022100619481685309877

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

Last update: 15.08.2025, 7:31 AM CEST

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Associated

Pickles, Sarah
Gendron, Tania F.
Koike, Yuka
Yue, Mei
Song, Yuping
Kachergus, Jennifer M.
Shi, J.
DeTure, Michael
Thompson, E. Aubrey
Oskarsson, Björn
Graff-Radford, Neill R.
Boeve, Bradley F.
Petersen, Ronald C.
Wszolek, Zbigniew K.
Josephs, Keith A.
Dickson, Dennis W.
Petrucelli, Leonard
Cook, Casey N.
Prudencio, Mercedes
SpringerLink (Online service)

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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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Aberrant deposition of stress granule-resident proteins linked to C9orf72-associated TDP-43 proteinopathy

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Evidence of cerebellar TDP-43 loss of function in FTLD-TDP

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Other Objects (12)

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

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

Expression of mutant TDP-43 induces neuronal dysfunction in transgenic mice

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

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

The neuropathological diagnosis of Alzheimer’s disease

Aberrant deposition of stress granule-resident proteins linked to C9orf72-associated TDP-43 proteinopathy

Does a loss of TDP-43 function cause neurodegeneration?

TDP-43-regulated cryptic RNAs accumulate in Alzheimer’s disease brains

The effect of TDP-43 antibodies on TDP-43 aggregation and toxicity

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

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

TDP-43 Pathology in Alzheimer’s Disease

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

Expression of mutant TDP-43 induces neuronal dysfunction in transgenic mice

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

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

The neuropathological diagnosis of Alzheimer’s disease

Aberrant deposition of stress granule-resident proteins linked to C9orf72-associated TDP-43 proteinopathy

Does a loss of TDP-43 function cause neurodegeneration?

TDP-43-regulated cryptic RNAs accumulate in Alzheimer’s disease brains

The effect of TDP-43 antibodies on TDP-43 aggregation and toxicity

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

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

TDP-43 Pathology in Alzheimer’s Disease

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

Expression of mutant TDP-43 induces neuronal dysfunction in transgenic mice

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

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

The neuropathological diagnosis of Alzheimer’s disease

Aberrant deposition of stress granule-resident proteins linked to C9orf72-associated TDP-43 proteinopathy

Does a loss of TDP-43 function cause neurodegeneration?

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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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