Biomarkers for diseases with TDP-43 pathology
P Steinacker, P Barschke, M Otto - Molecular and Cellular Neuroscience, 2019 - Elsevier
The discovery that aggregated transactive response DNA-binding protein 43 kDa (TDP-43)
is the major component of pathological ubiquitinated inclusions in amyotrophic lateral …
is the major component of pathological ubiquitinated inclusions in amyotrophic lateral …
Amyotrophic lateral sclerosis, frontotemporal dementia and beyond: the TDP-43 diseases
F Geser, M Martinez-Lage, LK Kwong, VMY Lee… - Journal of …, 2009 - Springer
Ever since the significance of pathological 43-kDa transactivating responsive sequence
DNA-binding protein (TDP-43) for human disease has been recognized in amyotrophic …
DNA-binding protein (TDP-43) for human disease has been recognized in amyotrophic …
TDP-43 proteinopathy: the neuropathology underlying major forms of sporadic and familial frontotemporal lobar degeneration and motor neuron disease
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 …
that transactive response (TAR)-DNA-binding protein 43 (TDP-43) is the major disease …
Molecular neuropathology of TDP-43 proteinopathies
M Neumann - International journal of molecular sciences, 2009 - mdpi.com
The identification of TDP-43 as the major component of the pathologic inclusions in most
forms of sporadic and familial frontotemporal lobar degeneration with ubiquitin-positive …
forms of sporadic and familial frontotemporal lobar degeneration with ubiquitin-positive …
TDP-43 proteinopathies: neurodegenerative protein misfolding diseases without amyloidosis
LK Kwong, K Uryu, JQ Trojanowski, VMY Lee - Neurosignals, 2007 - karger.com
In this review, we summarize recent advances in understanding frontotemporal lobar
degeneration (FTLD), amyotrophic lateral sclerosis (ALS) and related neurodegenerative …
degeneration (FTLD), amyotrophic lateral sclerosis (ALS) and related neurodegenerative …
The basis of clinicopathological heterogeneity in TDP-43 proteinopathy
I Kawakami, T Arai, M Hasegawa - Acta neuropathologica, 2019 - Springer
Transactive response DNA-binding protein 43 kDa (TDP-43) was identified as a major
disease-associated component in the brain of patients with amyotrophic lateral sclerosis …
disease-associated component in the brain of patients with amyotrophic lateral sclerosis …
TDP-43 proteinopathy specific biomarker development
TDP-43 is the primary or secondary pathological hallmark of neurodegenerative diseases,
such as amyotrophic lateral sclerosis, half of frontotemporal dementia cases, and limbic age …
such as amyotrophic lateral sclerosis, half of frontotemporal dementia cases, and limbic age …
On the development of markers for pathological TDP-43 in amyotrophic lateral sclerosis with and without dementia
F Geser, D Prvulovic, L O'Dwyer, O Hardiman… - Progress in …, 2011 - Elsevier
Pathological 43-kDa transactive response sequence DNA-binding protein (TDP-43) has
been recognized as the major disease protein in amyotrophic lateral sclerosis (ALS) …
been recognized as the major disease protein in amyotrophic lateral sclerosis (ALS) …
Data-driven neuropathological staging and subtyping of TDP-43 proteinopathies
Abstract TAR DNA-binding protein-43 (TDP-43) accumulation is the primary pathology
underlying several neurodegenerative diseases. Charting the progression and …
underlying several neurodegenerative diseases. Charting the progression and …
Pathological mechanisms underlying TDP-43 driven neurodegeneration in FTLD–ALS spectrum disorders
J Janssens, C Van Broeckhoven - Human molecular genetics, 2013 - academic.oup.com
Aggregation of misfolded TAR DNA-binding protein 43 (TDP-43) is a striking hallmark of
neurodegenerative processes that are observed in several neurological disorders, and in …
neurodegenerative processes that are observed in several neurological disorders, and in …