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A Huntington disease-like neurodegenerative disorder maps to chromosome 20p.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1377554
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9792871%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
title
A Huntington disease-like neurodegenerative disorder maps to chromosome 20p
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1377554
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9792871%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
main subject
Huntington's disease
0 references
neurodegeneration
1 reference
based on heuristic
inferred from title
author
Fengqing Xiang
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1377554
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9792871%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
Michael R. Hayden
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMC publication ID
1377554
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9792871%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
author name string
Almqvist EW
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1377554
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9792871%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
Huq M
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1377554
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9792871%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
Lundin A
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
1377554
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9792871%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
Edström L
series ordinal
6
1 reference
stated in
Europe PubMed Central
PMC publication ID
1377554
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9792871%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
Anvret M
series ordinal
7
1 reference
stated in
Europe PubMed Central
PMC publication ID
1377554
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9792871%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
Zhang Z
series ordinal
8
1 reference
stated in
Europe PubMed Central
PMC publication ID
1377554
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9792871%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
language of work or name
English
0 references
publication date
1 November 1998
1 reference
stated in
Europe PubMed Central
PMC publication ID
1377554
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9792871%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1377554
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9792871%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
volume
63
1 reference
stated in
Europe PubMed Central
PMC publication ID
1377554
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9792871%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
issue
5
1 reference
stated in
Europe PubMed Central
PMC publication ID
1377554
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9792871%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
page(s)
1431-1438
1 reference
stated in
Europe PubMed Central
PMC publication ID
1377554
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9792871%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
cites work
Length of huntingtin and its polyglutamine tract influences localization and frequency of intracellular aggregates
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377554
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6 July 2018
Intranuclear neuronal inclusions: a common pathogenic mechanism for glutamine-repeat neurodegenerative diseases?
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PubMed Central
reference URL
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6 July 2018
The complex pathology of trinucleotide repeats
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PubMed Central
reference URL
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6 July 2018
HIP1, a human homologue of S. cerevisiae Sla2p, interacts with membrane-associated huntingtin in the brain
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stated in
PubMed Central
reference URL
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6 July 2018
Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13
1 reference
stated in
PubMed Central
reference URL
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6 July 2018
Linkage of frontotemporal dementia to chromosome 17: clinical and neuropathological characterization of phenotype
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6 July 2018
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6 July 2018
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6 July 2018
Faster sequential genetic linkage computations
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PubMed Central
reference URL
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6 July 2018
Huntington disease without CAG expansion: phenocopies or errors in assignment?
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377554
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6 July 2018
A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeats
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377554
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6 July 2018
Cloning and sequence analysis of the human SNAP25 cDNA
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6 July 2018
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6 July 2018
Isolation and structural organization of the human preproenkephalin B gene
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6 July 2018
A point mutation in the coding region of uroporphyrinogen decarboxylase associated with familial porphyria cutanea tarda
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6 July 2018
Genomic structure of the human prion protein gene
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377554
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6 July 2018
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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377554
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Hereditary frontotemporal dementia is linked to chromosome 17q21?q22: A genetic and clinicopathological study of three dutch families
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reference URL
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9 December 2018
Prevalence of the 281 (Gly----Glu) mutation in hepatoerythropoietic porphyria and porphyria cutanea tarda
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9792871
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1086/302093
1 reference
stated in
Europe PubMed Central
PMC publication ID
1377554
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9792871%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
PMC publication ID
1377554
1 reference
stated in
Europe PubMed Central
PMC publication ID
1377554
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9792871%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
PubMed publication ID
9792871
1 reference
stated in
Europe PubMed Central
PMC publication ID
1377554
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9792871%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
ResearchGate publication ID
13493290
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