Correction: HDGFL2 cryptic proteins report presence of TDP-43 pathology in neurodegenerative diseases

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Correction: HDGFL2 cryptic proteins report presence of TDP-43 pathology in neurodegenerative diseases ; volume:19 ; number:1 ; day:27 ; month:7 ; year:2024 ; pages:1-2 ; date:12.2024
Molecular neurodegeneration ; 19, Heft 1 (27.7.2024), 1-2, 12.2024

Creator: Calliari, Anna
Daughrity, Lillian M.
Albagli, Ellen A.
Castellanos Otero, Paula
Yue, Mei
Jansen-West, Karen
Islam, Naeyma N.
Caulfield, Thomas
Rawlinson, Bailey
DeTure, Michael
Cook, Casey
Graff-Radford, Neill R.
Day, Gregory S.
Boeve, Bradley F.
Knopman, David S.
Petersen, Ronald C.
Josephs, Keith A.
Oskarsson, Björn
Gitler, Aaron D.
Dickson, Dennis W.
Gendron, Tania F.
Prudencio, Mercedes
Ward, Michael E.
Zhang, Yong-Jie
Petrucelli, Leonard

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13024-024-00744-6

URN: urn:nbn:de:101:1-2410122120132.146719312534

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

Last update: 15.08.2025, 7:29 AM CEST

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Associated

Calliari, Anna
Daughrity, Lillian M.
Albagli, Ellen A.
Castellanos Otero, Paula
Yue, Mei
Jansen-West, Karen
Islam, Naeyma N.
Caulfield, Thomas
Rawlinson, Bailey
DeTure, Michael
Cook, Casey
Graff-Radford, Neill R.
Day, Gregory S.
Boeve, Bradley F.
Knopman, David S.
Petersen, Ronald C.
Josephs, Keith A.
Oskarsson, Björn
Gitler, Aaron D.
Dickson, Dennis W.
Gendron, Tania F.
Prudencio, Mercedes
Ward, Michael E.
Zhang, Yong-Jie
Petrucelli, Leonard
SpringerLink (Online service)

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HDGFL2 cryptic proteins report presence of TDP-43 pathology in neurodegenerative diseases

TDP-43 Pathology in Alzheimer’s Disease

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

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

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

Molecular fragment characteristics and distribution of tangle associated TDP-43 (TATs) and other TDP-43 lesions 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

Altered microRNA expression in frontotemporal lobar degeneration with TDP-43 pathology caused by progranulin mutations

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

Cellular and pathological heterogeneity of primary tauopathies

Znf179 E3 ligase-mediated TDP-43 polyubiquitination is involved in TDP-43- ubiquitinated inclusions (UBI) (+)-related neurodegenerative pathology

HDGFL2 cryptic proteins report presence of TDP-43 pathology in neurodegenerative diseases

TDP-43 Pathology in Alzheimer’s Disease

The neuropathological diagnosis of Alzheimer’s disease

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

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

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

Molecular fragment characteristics and distribution of tangle associated TDP-43 (TATs) and other TDP-43 lesions 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

Altered microRNA expression in frontotemporal lobar degeneration with TDP-43 pathology caused by progranulin mutations

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

Cellular and pathological heterogeneity of primary tauopathies

Znf179 E3 ligase-mediated TDP-43 polyubiquitination is involved in TDP-43- ubiquitinated inclusions (UBI) (+)-related neurodegenerative pathology

HDGFL2 cryptic proteins report presence of TDP-43 pathology in neurodegenerative diseases

TDP-43 Pathology in Alzheimer’s Disease

The neuropathological diagnosis of Alzheimer’s disease

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

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

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

Molecular fragment characteristics and distribution of tangle associated TDP-43 (TATs) and other TDP-43 lesions 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

Altered microRNA expression in frontotemporal lobar degeneration with TDP-43 pathology caused by progranulin mutations

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

Cellular and pathological heterogeneity of primary tauopathies

Znf179 E3 ligase-mediated TDP-43 polyubiquitination is involved in TDP-43- ubiquitinated inclusions (UBI) (+)-related neurodegenerative pathology

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Correction: HDGFL2 cryptic proteins report presence of TDP-43 pathology in neurodegenerative diseases

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Other Objects (12)

HDGFL2 cryptic proteins report presence of TDP-43 pathology in neurodegenerative diseases

TDP-43 Pathology in Alzheimer’s Disease

The neuropathological diagnosis of Alzheimer’s disease

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

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

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

Molecular fragment characteristics and distribution of tangle associated TDP-43 (TATs) and other TDP-43 lesions 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

Altered microRNA expression in frontotemporal lobar degeneration with TDP-43 pathology caused by progranulin mutations

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

Cellular and pathological heterogeneity of primary tauopathies

Znf179 E3 ligase-mediated TDP-43 polyubiquitination is involved in TDP-43- ubiquitinated inclusions (UBI) (+)-related neurodegenerative pathology

HDGFL2 cryptic proteins report presence of TDP-43 pathology in neurodegenerative diseases

TDP-43 Pathology in Alzheimer’s Disease

The neuropathological diagnosis of Alzheimer’s disease

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

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

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

Molecular fragment characteristics and distribution of tangle associated TDP-43 (TATs) and other TDP-43 lesions 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

Altered microRNA expression in frontotemporal lobar degeneration with TDP-43 pathology caused by progranulin mutations

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

Cellular and pathological heterogeneity of primary tauopathies

Znf179 E3 ligase-mediated TDP-43 polyubiquitination is involved in TDP-43- ubiquitinated inclusions (UBI) (+)-related neurodegenerative pathology

HDGFL2 cryptic proteins report presence of TDP-43 pathology in neurodegenerative diseases

TDP-43 Pathology in Alzheimer’s Disease

The neuropathological diagnosis of Alzheimer’s disease

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

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

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

Molecular fragment characteristics and distribution of tangle associated TDP-43 (TATs) and other TDP-43 lesions 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

Altered microRNA expression in frontotemporal lobar degeneration with TDP-43 pathology caused by progranulin mutations

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

Cellular and pathological heterogeneity of primary tauopathies

Znf179 E3 ligase-mediated TDP-43 polyubiquitination is involved in TDP-43- ubiquitinated inclusions (UBI) (+)-related neurodegenerative pathology

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