Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
<sup>18</sup>F-Flortaucipir in TDP-43 associated frontotemporal dementia.
|
30988363 |
2019 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
Frontotemporal dementia and amyotrophic lateral sclerosis-associated disease protein TDP-43 promotes dendritic branching.
|
19781077 |
2009 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
Frontotemporal dementia is a group of early onset dementia syndromes linked to underlying frontotemporal lobar degeneration (FTLD) pathology that can be classified based on the formation of abnormal protein aggregates involving tau and two RNA binding proteins, TDP-43 and FUS.
|
30355151 |
2019 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
Frontotemporal dementia-associated protein "phosphorylated TDP-43" localizes to atherosclerotic lesions of human carotid and main cerebral arteries.
|
31259382 |
2020 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations.
|
17279000 |
2007 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia.
|
18796596 |
2008 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
TDP-43 was recently identified as the major pathological protein in sporadic amyotrophic lateral sclerosis and in the most common pathological subtype of frontotemporal dementia, frontotemporal lobar degeneration with ubiquitinated inclusions.
|
18989115 |
2008 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
TAR DNA binding protein 43 (TDP-43) has been considered a signature protein in frontotemporal dementia and amyotrophic lateral sclerosis (ALS), but not in ALS associated with the superoxide dismutase 1 (SOD1) gene mutations (ALS1).
|
19104447 |
2009 |
Pick Disease of the Brain
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea.
|
19609911 |
2009 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
TDP-43 and frontotemporal dementia.
|
19664364 |
2009 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia.
|
20864052 |
2010 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
TDP-43 is a multifunctional nucleic acid binding protein linked to several neurodegenerative diseases including Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia.
|
22792076 |
2012 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
TAR DNA-binding protein-43 (TDP-43) is the principal component of ubiquitinated inclusions in amyotrophic lateral sclerosis (ALS) and the most common pathological subtype of frontotemporal dementia-frontotemporal lobar degeneration with TDP-43-positive inclusions (FTLD-TDP).
|
23575225 |
2013 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
TDP-43 (TAR DNA-binding protein of 43 kDa) is a major deposited protein in amyotrophic lateral sclerosis and frontotemporal dementia with ubiquitin.
|
23689371 |
2013 |
Pick Disease of the Brain
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
TARDBP mutation screening should be considered in familial frontotemporal dementia cases, even without signs or symptoms of motor neuron disease, especially when other more frequent causes of genetic frontotemporal dementia (i.e.
|
25853458 |
2015 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
TDP-43 is a primarily nuclear RNA-binding protein, whose abnormal phosphorylation and cytoplasmic aggregation characterizes affected neurons in patients with amyotrophic lateral sclerosis and frontotemporal dementia.
|
28663553 |
2017 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
TDP43 nuclear export and neurodegeneration in models of amyotrophic lateral sclerosis and frontotemporal dementia.
|
29545601 |
2018 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
TAR DNA-binding protein of 43 kDa (TDP-43) forms pathological aggregates in neurodegenerative diseases, particularly in certain forms of frontotemporal dementia and amyotrophic lateral sclerosis.
|
30120199 |
2018 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
TDP-43 inclusions also characterize patients with GGGGCC (G4C2) hexanucleotide repeat expansion in C9orf72 that causes the most common genetic form of amyotrophic lateral sclerosis and frontotemporal dementia (C9ALS/FTD).
|
30239641 |
2018 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
TAR DNA-binding protein 43 (TDP-43) is a major protein component of pathological inclusions in amyotrophic lateral sclerosis and frontotemporal dementia.
|
30372676 |
2018 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
A common pathological hallmark of amyotrophic lateral sclerosis (ALS) and the related neurodegenerative disorder frontotemporal dementia, is the cellular mislocalization of transactive response DNA-binding protein 43 kDa (TDP-43).
|
31642482 |
2019 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
A similar distribution of TDP-43 inclusions is seen in sporadic Alzheimer disease, but it differs from that seen in amyotrophic lateral sclerosis and frontotemporal dementia.
|
20008652 |
2009 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
Abnormal neuronal accumulation and modification of TAR DNA binding protein 43 (TDP-43) have recently been discovered to be defining histopathological features of particular subtypes of frontotemporal dementia and amyotrophic lateral sclerosis, and are also common in aging, particularly coexisting with hippocampal sclerosis and Alzheimer's disease pathology.
|
24927705 |
2014 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
Accumulation of TDP-43 in the cytoplasm of diseased neurons is the pathological hallmark of frontotemporal dementia-TDP (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), two diseases that lack efficacious medicine to prevent or to stop disease progression.
|
30785719 |
2019 |
Pick Disease of the Brain
|
0.100 |
Biomarker
|
disease |
BEFREE |
Aggregates of the RNA-binding protein TDP-43 (TAR DNA-binding protein) are a hallmark of the overlapping neurodegenerative disorders amyotrophic lateral sclerosis (ALS) and frontotemporal dementia.
|
30824544 |
2019 |