Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43.
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Progranulin in frontotemporal lobar degeneration and neuroinflammationTDP-43 regulates retinoblastoma protein phosphorylation through the repression of cyclin-dependent kinase 6 expressionTARDBP mutation analysis in TDP-43 proteinopathies and deciphering the toxicity of mutant TDP-43A harmonized classification system for FTLD-TDP pathologyWord-finding difficulty: a clinical analysis of the progressive aphasias.A new subtype of frontotemporal lobar degeneration with FUS pathologyRapamycin rescues TDP-43 mislocalization and the associated low molecular mass neurofilament instabilityProgranulin: normal function and role in neurodegenerationNovel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosisA 43-kDa TDP-43 species is present in aggregates associated with frontotemporal lobar degenerationβ-amyloid triggers ALS-associated TDP-43 pathology in AD modelsA90V TDP-43 variant results in the aberrant localization of TDP-43 in vitro.VCP mutations causing frontotemporal lobar degeneration disrupt localization of TDP-43 and induce cell death.TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration.Neuropathology of Amyotrophic Lateral Sclerosis and Its Variants.Plasma phosphorylated-TDP-43 protein levels correlate with brain pathology in frontotemporal lobar degeneration.Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar DegenerationNeuropathological heterogeneity in frontotemporal lobar degeneration with TDP-43 proteinopathy: a quantitative study of 94 cases using principal components analysisClassification of FTLD-TDP cases into pathological subtypes using antibodies against phosphorylated and non-phosphorylated TDP43.Overexpression of the essential Sis1 chaperone reduces TDP-43 effects on toxicity and proteolysis.The acoustic cortex in frontotemporal dementia: a Golgi and electron microscope study.Modeling the association between 43 different clinical and pathological variables and the severity of cognitive impairment in a large autopsy cohort of elderly persons.The role of transactive response DNA-binding protein-43 in amyotrophic lateral sclerosis and frontotemporal dementia.TAR DNA-binding protein 43 in neurodegenerative disease.Phosphorylated TDP-43 pathology and hippocampal sclerosis in progressive supranuclear palsyTDP-43 pathology in primary progressive aphasia and frontotemporal dementia with pathologic Alzheimer disease.Neurotoxic effects of TDP-43 overexpression in C. elegans.Distinct pathological subtypes of FTLD-FUS.Poly-A binding protein-1 localization to a subset of TDP-43 inclusions in amyotrophic lateral sclerosis occurs more frequently in patients harboring an expansion in C9orf72Early retinal neurodegeneration and impaired Ran-mediated nuclear import of TDP-43 in progranulin-deficient FTLDA morphometric study of the spatial patterns of TDP-43 immunoreactive neuronal inclusions in frontotemporal lobar degeneration (FTLD) with progranulin (GRN) mutation.Transcription factors expressed in olfactory bulb local progenitor cells revealed by genome-wide transcriptome profiling.Evaluation of subcortical pathology and clinical correlations in FTLD-U subtypes.Review: transactive response DNA-binding protein 43 (TDP-43): mechanisms of neurodegeneration.p53 and Cell Cycle Proteins Participate in Spinal Motor Neuron Cell Death in ALSHippocampal sclerosis in advanced age: clinical and pathological features.Expression of one important chaperone protein, heat shock protein 27, in neurodegenerative diseases.Granular expression of prolyl-peptidyl isomerase PIN1 is a constant and specific feature of Alzheimer's disease pathology and is independent of tau, Aβ and TDP-43 pathologyAmyotrophic lateral sclerosis and frontotemporal lobar degeneration: a spectrum of TDP-43 proteinopathies.A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathies
P2860
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P2860
Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43.
description
2007 nî lūn-bûn
@nan
2007 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Ubiquitinated pathological les ...... R DNA-binding protein, TDP-43.
@ast
Ubiquitinated pathological les ...... R DNA-binding protein, TDP-43.
@en
Ubiquitinated pathological les ...... R DNA-binding protein, TDP-43.
@nl
type
label
Ubiquitinated pathological les ...... R DNA-binding protein, TDP-43.
@ast
Ubiquitinated pathological les ...... R DNA-binding protein, TDP-43.
@en
Ubiquitinated pathological les ...... R DNA-binding protein, TDP-43.
@nl
prefLabel
Ubiquitinated pathological les ...... R DNA-binding protein, TDP-43.
@ast
Ubiquitinated pathological les ...... R DNA-binding protein, TDP-43.
@en
Ubiquitinated pathological les ...... R DNA-binding protein, TDP-43.
@nl
P2093
P1476
Ubiquitinated pathological les ...... R DNA-binding protein, TDP-43.
@en
P2093
Daniel Du Plessis
David M A Mann
David Neary
Ian R A Mackenzie
Thomas Kelley
Yvonne Davidson
P2860
P2888
P304
P356
10.1007/S00401-006-0189-Y
P577
2007-01-12T00:00:00Z