Lack of TAR-DNA binding protein-43 (TDP-43) pathology in human prion diseases.
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Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathyFilamentous white matter prion protein deposition is a distinctive feature of multiple inherited prion diseasesDisruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutations.Prion protein codon 129 polymorphism modifies age at onset of frontotemporal dementia with the C.709-1G>A progranulin mutation.Amyotrophic lateral sclerosis, frontotemporal dementia and beyond: the TDP-43 diseases.Molecular pathology of human prion diseases.De novo prion aggregates trigger autophagy in skeletal muscle.TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration.Oral biomarkers in exercise-induced neuroplasticity in Parkinson's disease.Tau pathology in Creutzfeldt-Jakob disease revisited.
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Lack of TAR-DNA binding protein-43 (TDP-43) pathology in human prion diseases.
description
article científic
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article scientifique
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articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on August 2008
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Lack of TAR-DNA binding protein-43 (TDP-43) pathology in human prion diseases.
@en
Lack of TAR-DNA binding protein-43
@nl
type
label
Lack of TAR-DNA binding protein-43 (TDP-43) pathology in human prion diseases.
@en
Lack of TAR-DNA binding protein-43
@nl
prefLabel
Lack of TAR-DNA binding protein-43 (TDP-43) pathology in human prion diseases.
@en
Lack of TAR-DNA binding protein-43
@nl
P2093
P2860
P1476
Lack of TAR-DNA binding protein-43 (TDP-43) pathology in human prion diseases
@en
P2093
A M Isaacs
J Collinge
J M Linehan
S Brandner
P2860
P304
P356
10.1111/J.1365-2990.2008.00963.X
P50
P577
2008-08-01T00:00:00Z