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

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource, 1 online resource.

Language: Englisch

Bibliographic citation: TDP-43-regulated cryptic RNAs accumulate in Alzheimer’s disease brains ; volume:18 ; number:1 ; day:21 ; month:8 ; year:2023 ; pages:1-13 ; date:12.2023
Molecular neurodegeneration ; 18, Heft 1 (21.8.2023), 1-13, 12.2023

Creator: Estades Ayuso, Virginia
Pickles, Sarah
Todd, Tiffany
Yue, Mei
Jansen-West, Karen
Song, Yuping
González Bejarano, Jesús
Rawlinson, Bailey
DeTure, Michael
Graff-Radford, Neill R.
Boeve, Bradley F.
Knopman, David S.
Petersen, Ronald C.
Dickson, Dennis W.
Josephs, Keith A.
Petrucelli, Leonard
Prudencio, Mercedes

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13024-023-00646-z

URN: urn:nbn:de:101:1-2023110608001911858960

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

Last update: 14.08.2025, 11:00 AM CEST

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Associated

Estades Ayuso, Virginia
Pickles, Sarah
Todd, Tiffany
Yue, Mei
Jansen-West, Karen
Song, Yuping
González Bejarano, Jesús
Rawlinson, Bailey
DeTure, Michael
Graff-Radford, Neill R.
Boeve, Bradley F.
Knopman, David S.
Petersen, Ronald C.
Dickson, Dennis W.
Josephs, Keith A.
Petrucelli, Leonard
Prudencio, Mercedes
SpringerLink (Online service)

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The neuropathological diagnosis of Alzheimer’s disease

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

Cryptic splicing of stathmin-2 and UNC13A mRNAs is a pathological hallmark of TDP-43-associated 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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Tau isoforms are differentially expressed across the hippocampus in chronic traumatic encephalopathy and Alzheimer’s disease

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Sex and age interact to determine clinicopathologic differences in Alzheimer’s disease

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The neuropathological diagnosis of 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

Expression and processing analyses of wild type and p.R47H TREM2 variant in Alzheimer’s disease brains

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

Sex and age interact to determine clinicopathologic differences in Alzheimer’s disease

Correction to: Deciphering cellular transcriptional alterations in Alzheimer’s disease brains

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

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Other Objects (12)

The neuropathological diagnosis of Alzheimer’s disease

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

Cryptic splicing of stathmin-2 and UNC13A mRNAs is a pathological hallmark of TDP-43-associated Alzheimer’s disease

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

Expression and processing analyses of wild type and p.R47H TREM2 variant in Alzheimer’s disease brains

Tau isoforms are differentially expressed across the hippocampus in chronic traumatic encephalopathy and Alzheimer’s disease

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

Sex and age interact to determine clinicopathologic differences in Alzheimer’s disease

Correction to: Deciphering cellular transcriptional alterations in Alzheimer’s disease brains

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

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

Cryptic splicing of stathmin-2 and UNC13A mRNAs is a pathological hallmark of TDP-43-associated Alzheimer’s disease

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

Expression and processing analyses of wild type and p.R47H TREM2 variant in Alzheimer’s disease brains

Tau isoforms are differentially expressed across the hippocampus in chronic traumatic encephalopathy and Alzheimer’s disease

Deciphering cellular transcriptional alterations in Alzheimer’s disease brains

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

Sex and age interact to determine clinicopathologic differences in Alzheimer’s disease

Correction to: Deciphering cellular transcriptional alterations in Alzheimer’s disease brains

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

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

Cryptic splicing of stathmin-2 and UNC13A mRNAs is a pathological hallmark of TDP-43-associated Alzheimer’s disease

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

Expression and processing analyses of wild type and p.R47H TREM2 variant in Alzheimer’s disease brains

Tau isoforms are differentially expressed across the hippocampus in chronic traumatic encephalopathy and Alzheimer’s disease

Deciphering cellular transcriptional alterations in Alzheimer’s disease brains

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

Sex and age interact to determine clinicopathologic differences in Alzheimer’s disease

Correction to: Deciphering cellular transcriptional alterations in Alzheimer’s disease brains

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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