alpha-Internexin aggregates are abundant in neuronal intermediate filament inclusion disease (NIFID) but rare in other neurodegenerative diseases
about
Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion diseaseDysfunctions of neuronal and glial intermediate filaments in diseaseUncovering molecular biomarkers that correlate cognitive decline with the changes of hippocampus' gene expression profiles in Alzheimer's disease.Neuronal intranuclear inclusions are ultrastructurally and immunologically distinct from cytoplasmic inclusions of neuronal intermediate filament inclusion diseaseAnti-alpha-internexin autoantibody from neuropsychiatric lupus induce cognitive damage via inhibiting axonal elongation and promote neuron apoptosis.FUS immunogold labeling TEM analysis of the neuronal cytoplasmic inclusions of neuronal intermediate filament inclusion disease: a frontotemporal lobar degeneration with FUS proteinopathy.FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration.Identification and characterization of a novel endogenous murine parkin mutation.Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update.Suppression of extensive neurofilament phosphorylation rescues α-Internexin/peripherin-overexpressing PC12 cells from neuronal cell death.The cytoskeleton in neurodegenerative diseases.Clinical and neuropathologic variation in neuronal intermediate filament inclusion diseaseModest loss of peripheral axons, muscle atrophy and formation of brain inclusions in mice with targeted deletion of gigaxonin exon 1The molecular basis of frontotemporal dementia.Novel types of frontotemporal lobar degeneration: beyond tau and TDP-43.Gigaxonin mutation analysis in patients with NIFID.Expression pattern of neuronal intermediate filament α-internexin in anterior pituitary gland and related tumors.Proteomic identification of novel proteins in cortical lewy bodies.Fronto-temporal lobar degeneration: neuropathology in 60 cases.
P2860
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P2860
alpha-Internexin aggregates are abundant in neuronal intermediate filament inclusion disease (NIFID) but rare in other neurodegenerative diseases
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
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2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
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2004年學術文章
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name
alpha-Internexin aggregates ar ...... her neurodegenerative diseases
@ast
alpha-Internexin aggregates ar ...... her neurodegenerative diseases
@en
type
label
alpha-Internexin aggregates ar ...... her neurodegenerative diseases
@ast
alpha-Internexin aggregates ar ...... her neurodegenerative diseases
@en
prefLabel
alpha-Internexin aggregates ar ...... her neurodegenerative diseases
@ast
alpha-Internexin aggregates ar ...... her neurodegenerative diseases
@en
P2093
P2860
P1476
alpha-Internexin aggregates ar ...... her neurodegenerative diseases
@en
P2093
Charles Duyckaerts
Eileen H Bigio
Evelyn Jaros
Hideaki Yokoo
Ian R A Mackenzie
Kunihiro Uryu
Marla Gearing
Nigel J Cairns
Robert H Perry
Virginia M-Y Lee
P2860
P2888
P304
P356
10.1007/S00401-004-0882-7
P577
2004-05-28T00:00:00Z