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Filamentous nerve cell inclusions in neurodegenerative diseases
scientific article published on 01 October 1998
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
9811617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9811617%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
review article
1 reference
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Europe PubMed Central
title
Filamentous nerve cell inclusions in neurodegenerative diseases
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
9811617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9811617%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
author name string
M Goedert
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
9811617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9811617%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
M G Spillantini
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
9811617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9811617%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
S W Davies
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
9811617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9811617%20AND%20SRC:MED&resulttype=core&format=json
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6 December 2019
publication date
1 October 1998
1 reference
stated in
Europe PubMed Central
PubMed ID
9811617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9811617%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
published in
Current Opinion in Neurobiology
1 reference
stated in
Europe PubMed Central
PubMed ID
9811617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9811617%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
volume
8
1 reference
stated in
Europe PubMed Central
PubMed ID
9811617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9811617%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
issue
5
1 reference
stated in
Europe PubMed Central
PubMed ID
9811617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9811617%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
page(s)
619-632
1 reference
stated in
Europe PubMed Central
PubMed ID
9811617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9811617%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
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Mutant genes in familial Alzheimer's disease and transgenic models
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Secreted amyloid beta-protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease
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Accelerated Alzheimer-type phenotype in transgenic mice carrying both mutant amyloid precursor protein and presenilin 1 transgenes
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LIN-12/Notch signaling: lessons from worms and flies
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Increased amyloid beta-peptide deposition in cerebral cortex as a consequence of apolipoprotein E genotype in late-onset Alzheimer disease
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APPSw transgenic mice develop age-related A beta deposits and neuropil abnormalities, but no neuronal loss in CA1.
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7 January 2021
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Vulnerable neuronal subsets in Alzheimer's and Pick's disease are distinguished by their tau isoform distribution and phosphorylation.
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7 January 2021
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Pick's disease: hyperphosphorylated tau protein segregates to the somatoaxonal compartment.
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Frontotemporal dementia and Parkinsonism linked to chromosome 17: a new group of tauopathies.
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Comparison of the neurofibrillary pathology in Alzheimer's disease and familial presenile dementia with tangles
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Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments
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The neuropathology of a chromosome 17-linked autosomal dominant parkinsonism and dementia ("pallido-ponto-nigral degeneration").
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Genetic evidence for the involvement of tau in progressive supranuclear palsy
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Progressive supranuclear gaze palsy is in linkage disequilibrium with the tau and not the alpha-synuclein gene
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Tau is a candidate gene for chromosome 17 frontotemporal dementia
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Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17
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Mutation in the tau gene in familial multiple system tauopathy with presenile dementia
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7 January 2021
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Neuropathology of Parkinson's disease
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7 January 2021
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A large kindred with autosomal dominant Parkinson's disease
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7 January 2021
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Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
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Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease
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Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
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NACP, a protein implicated in Alzheimer's disease and learning, is natively unfolded
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7 January 2021
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Stabilization of alpha-synuclein secondary structure upon binding to synthetic membranes
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7 January 2021
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Alpha-synuclein in Lewy bodies
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NACP, a presynaptic protein, immunoreactivity in Lewy bodies in Parkinson's disease.
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7 January 2021
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Nigral and cortical Lewy bodies and dystrophic nigral neurites in Parkinson's disease and cortical Lewy body disease contain alpha-synuclein immunoreactivity.
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alpha-Synuclein in filamentous inclusions of Lewy bodies from Parkinson's disease and dementia with lewy bodies
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Dementia with Lewy bodies. A distinct non-Alzheimer dementia syndrome?
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7 January 2021
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The distribution of oligodendroglial inclusions in multiple system atrophy and its relevance to clinical symptomatology.
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7 January 2021
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Alpha-synuclein immunoreactivity in glial cytoplasmic inclusions in multiple system atrophy
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7 January 2021
based on heuristic
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Alpha synuclein in neurodegenerative disorders: murderer or accomplice?
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7 January 2021
based on heuristic
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Filamentous alpha-synuclein inclusions link multiple system atrophy with Parkinson's disease and dementia with Lewy bodies.
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https://api.crossref.org/works/10.1016%2FS0959-4388%2898%2980090-1
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7 January 2021
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Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
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7 January 2021
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Are neuronal intranuclear inclusions the common neuropathology of triplet-repeat disorders with polyglutamine-repeat expansions?
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Glutamine repeats as polar zippers: their possible role in inherited neurodegenerative diseases
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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.
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Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice
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7 January 2021
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Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation
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7 January 2021
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Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo
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7 January 2021
based on heuristic
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Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain
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https://api.crossref.org/works/10.1016%2FS0959-4388%2898%2980090-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3.
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0959-4388%2898%2980090-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structures
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7 January 2021
based on heuristic
inferred from DOI database lookup
Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1.
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https://api.crossref.org/works/10.1016%2FS0959-4388%2898%2980090-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Immunocytochemical co-localization of the proteasome in ubiquitinated structures in neurodegenerative diseases and the elderly.
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7 January 2021
based on heuristic
inferred from DOI database lookup
Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretch.
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https://api.crossref.org/works/10.1016%2FS0959-4388%2898%2980090-1
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7 January 2021
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inferred from DOI database lookup
Intranuclear neuronal inclusions in Huntington's disease and dentatorubral and pallidoluysian atrophy: correlation between the density of inclusions and IT15 CAG triplet repeat length
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Crossref
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https://api.crossref.org/works/10.1016%2FS0959-4388%2898%2980090-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Spinocerebellar ataxia type 7 (SCA7): a neurodegenerative disorder with neuronal intranuclear inclusions.
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-4388%2898%2980090-1
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7 January 2021
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Nuclear inclusions of the androgen receptor protein in spinal and bulbar muscular atrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-4388%2898%2980090-1
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7 January 2021
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Ectopically expressed CAG repeats cause intranuclear inclusions and a progressive late onset neurological phenotype in the mouse.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-4388%2898%2980090-1
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7 January 2021
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Expanded polyglutamine protein forms nuclear inclusions and causes neural degeneration in Drosophila.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-4388%2898%2980090-1
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7 January 2021
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Identifiers
DOI
10.1016/S0959-4388(98)80090-1
1 reference
stated in
Europe PubMed Central
PubMed ID
9811617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9811617%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
PubMed ID
9811617
1 reference
stated in
Europe PubMed Central
PubMed ID
9811617
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9811617%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
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