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 …

TDP-43 in cerebrospinal fluid of patients with frontotemporal lobar degeneration and amyotrophic lateral sclerosis

P Steinacker, C Hendrich, AD Sperfeld… - Archives of …, 2008 - jamanetwork.com
Background Recently, TAR DNA-binding protein 43 (TDP-43) was identified as the major
component of ubiquitin-positive tau-negative neuronal and glial inclusions in the most …

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 …

TAR DNA-binding protein 43 in neurodegenerative disease

AS Chen-Plotkin, VMY Lee… - Nature Reviews …, 2010 - nature.com
In 2006, TAR DNA-binding protein 43 (TDP-43), a highly conserved nuclear protein, was
identified as the major disease protein in amyotrophic lateral sclerosis (ALS) and in the most …

TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions

NJ Cairns, M Neumann, EH Bigio, IE Holm… - The American journal of …, 2007 - Elsevier
TAR DNA-binding protein 43 (TDP-43) is a major pathological protein of sporadic and
familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions …

TDP-43 proteinopathy: the neuropathology underlying major forms of sporadic and familial frontotemporal lobar degeneration and motor neuron disease

LK Kwong, M Neumann, DM Sampathu, VMY Lee… - Acta …, 2007 - Springer
The rapid confirmation of the initial report by Neumann et al.(Science 314: 130–133, 2006)
that transactive response (TAR)-DNA-binding protein 43 (TDP-43) is the major disease …

Disease-associated mutations of TDP-43 promote turnover of the protein through the proteasomal pathway

W Araki, S Minegishi, K Motoki, H Kume, H Hohjoh… - Molecular …, 2014 - Springer
Abstract TAR DNA-binding protein (TDP-43) is a major component of most ubiquitin-positive
neuronal and glial inclusions of amyotrophic lateral sclerosis (ALS) and frontotemporal lobar …

TDP-43 proteinopathy in frontotemporal lobar degeneration and amyotrophic lateral sclerosis: protein misfolding diseases without amyloidosis

M Neumann, LK Kwong, DM Sampathu… - Archives of …, 2007 - jamanetwork.com
Herein, we review advances in understanding a group of disorders collectively known as
TAR-DNA binding protein 43 (TDP-43) proteinopathies since the report that TDP-43 is the …

Severe subcortical TDP-43 pathology in sporadic frontotemporal lobar degeneration with motor neuron disease

NJ Brandmeir, F Geser, LK Kwong, E Zimmerman… - Acta …, 2008 - Springer
Abstract Recently, TDP-43, a 43 kDa nuclear TAR DNA-binding protein, was identified as
the major disease protein in frontotemporal lobar degeneration with ubiquitinated inclusions …

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 …