Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family.
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Valosin-containing protein and the pathogenesis of frontotemporal dementia associated with inclusion body myopathyTDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degenerationOverexpression of ALS-associated p.M337V human TDP-43 in mice worsens disease features compared to wild-type human TDP-43 mice.Familial dementia with frontotemporal features associated with M146V presenilin-1 mutationNeuropathological heterogeneity in frontotemporal lobar degeneration with TDP-43 proteinopathy: a quantitative study of 94 cases using principal components analysisMimicking aspects of frontotemporal lobar degeneration and Lou Gehrig's disease in rats via TDP-43 overexpression.FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration.A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder.A morphometric study of the spatial patterns of TDP-43 immunoreactive neuronal inclusions in frontotemporal lobar degeneration (FTLD) with progranulin (GRN) mutation.The spectrum and severity of FUS-immunoreactive inclusions in the frontal and temporal lobes of ten cases of neuronal intermediate filament inclusion disease.Abnormalities of the nucleus and nuclear inclusions in neurodegenerative disease: a work in progress.The complexities of p97 function in health and diseaseA quantitative study of the neuropathology of 32 sporadic and familial cases of frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP).Laminar distribution of the pathological changes in sporadic frontotemporal lobar degeneration with transactive response (TAR) DNA-binding protein of 43 kDa (TDP-43) proteinopathy: a quantitative study using polynomial curve fitting.Frontotemporal lobar degeneration: current concepts in the light of recent advances.Frontotemporal lobar degeneration with ubiquitin-positive inclusions: a molecular genetic update.Phenotypic variability in three families with valosin-containing protein mutation.Progranulin and TDP-43: mechanistic links and future directions.Increased caspase activation and decreased TDP-43 solubility in progranulin knockout cortical cultures.Cellular ageing, increased mortality and FTLD-TDP-associated neuropathology in progranulin knockout mice.Matrix metalloproteinase-9 expression in the nuclear compartment of neurons and glial cells in aging and stroke.Lipidomic and Transcriptomic Basis of Lysosomal Dysfunction in Progranulin Deficiency.Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortium.Cortical degeneration in frontotemporal lobar degeneration with TDP-43 proteinopathy caused by progranulin gene mutation.Drosophilaand Mouse Models of Hereditary Myopathy Caused by Mutations in VCP/p97
P2860
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P2860
Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh-hant
name
Characterization of ubiquitina ...... ral lobar degeneration family.
@en
Characterization of ubiquitina ...... ral lobar degeneration family.
@nl
type
label
Characterization of ubiquitina ...... ral lobar degeneration family.
@en
Characterization of ubiquitina ...... ral lobar degeneration family.
@nl
prefLabel
Characterization of ubiquitina ...... ral lobar degeneration family.
@en
Characterization of ubiquitina ...... ral lobar degeneration family.
@nl
P2093
P50
P1476
Characterization of ubiquitina ...... ral lobar degeneration family.
@en
P2093
Bart Dermaut
Chantal Ceuterick
Jean-Jacques Martin
Krist'l Vennekens
Marc Cruts
Rik Vandenberghe
Ursula Lübke
P304
P356
10.1097/01.JNEN.0000205147.39210.C7
P577
2006-03-01T00:00:00Z