An insoluble frontotemporal lobar degeneration-associated TDP-43 C-terminal fragment causes neurodegeneration and hippocampus pathology in transgenic mice

AK Walker, K Tripathy, CR Restrepo… - Human molecular …, 2015 - academic.oup.com
Frontotemporal dementia (FTD) causes progressive personality, behavior and/or language
disturbances and represents the second most common form of dementia under the age of …

[HTML][HTML] Neuronal sensitivity to TDP-43 overexpression is dependent on timing of induction

A Cannon, B Yang, J Knight, IM Farnham, Y Zhang… - Acta …, 2012 - Springer
Ubiquitin-immunoreactive neuronal inclusions composed of TAR DNA binding protein of 43
kDa (TDP-43) are a major pathological feature of frontotemporal lobar degeneration (FTLD …

Frontotemporal lobar degeneration with TAR DNA-binding protein 43 (TDP-43): its journey of more than 100 years

AF Carlos, KA Josephs - Journal of neurology, 2022 - Springer
Frontotemporal lobar degeneration (FTLD) with TDP-43-immunoreactive inclusions (FTLD–
TDP) is a neurodegenerative disease associated with clinical, genetic, and …

[HTML][HTML] Cognitive decline typical of frontotemporal lobar degeneration in transgenic mice expressing the 25-kDa C-terminal fragment of TDP-43

A Caccamo, S Majumder, S Oddo - The American journal of pathology, 2012 - Elsevier
Transactive response DNA-binding protein 43 (TDP-43) is the pathological signature protein
in several neurodegenerative disorders, including the majority of frontotemporal lobar …

TDP-43 and frontotemporal dementia

WT Hu, M Grossman - Current neurology and neuroscience reports, 2009 - Springer
TAR DNA-binding protein of about 43 kDa (TDP-43) is the main ubiquitinated peptide in tau-
negative frontotemporal lobar degeneration (FTLD). TDP-43 is typically a nuclear protein …

[HTML][HTML] Robust cytoplasmic accumulation of phosphorylated TDP-43 in transgenic models of tauopathy

AK Clippinger, S D'Alton, WL Lin, TF Gendron… - Acta …, 2013 - Springer
Frontotemporal lobar degeneration (FTLD) has been subdivided based on the main
pathology found in the brains of affected individuals. When the primary pathology is …

Distinct pathways leading to TDP-43-induced cellular dysfunctions

M Yamashita, T Nonaka, S Hirai, A Miwa… - Human molecular …, 2014 - academic.oup.com
TAR DNA-binding protein of 43 kDa (TDP-43) is the major component protein of inclusions
found in brains of patients with amyotrophic lateral sclerosis (ALS) and frontotemporal lobar …

[HTML][HTML] Early cognitive/social deficits and late motor phenotype in conditional wild-type TDP-43 transgenic mice

JA Alfieri, PR Silva, LM Igaz - Frontiers in Aging Neuroscience, 2016 - frontiersin.org
Frontotemporal Dementia (FTD) and amyotrophic lateral sclerosis (ALS) are two
neurodegenerative diseases associated to mislocalization and aggregation of TAR DNA …

[HTML][HTML] Transcriptomopathies of pre-and post-symptomatic frontotemporal dementia-like mice with TDP-43 depletion in forebrain neurons

LS Wu, WC Cheng, CY Chen, MC Wu… - Acta neuropathologica …, 2019 - Springer
Abstract TAR DNA-binding protein (TDP-43) is a ubiquitously expressed nuclear protein,
which participates in a number of cellular processes and has been identified as the major …

Elevated expression of TDP-43 in the forebrain of mice is sufficient to cause neurological and pathological phenotypes mimicking FTLD-U

KJ Tsai, CH Yang, YH Fang, KH Cho… - Journal of Experimental …, 2010 - rupress.org
TDP-43 is a multifunctional DNA/RNA-binding factor that has been implicated in the
regulation of neuronal plasticity. TDP-43 has also been identified as the major constituent of …