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English
The ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism does not confer protection against idiopathic Parkinson's disease.
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11027850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11027850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
title
The ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism does not confer protection against idiopathic Parkinson's disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11027850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11027850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
main subject
Parkinson's disease
1 reference
based on heuristic
inferred from title
author
George D. Mellick
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11027850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11027850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
author name string
P A Silburn
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11027850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11027850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
language of work or name
English
0 references
publication date
1 October 2000
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11027850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11027850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
published in
Neuroscience Letters
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11027850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11027850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
volume
293
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11027850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11027850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11027850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11027850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
page(s)
127-130
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11027850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11027850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
cites work
Criteria for diagnosing Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2800%2901510-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Q64866524
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2800%2901510-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A susceptibility locus for Parkinson's disease maps to chromosome 2p13.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2800%2901510-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2800%2901510-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The demonstration of new human brain-specific proteins by high-resolution two-dimensional polyacrylamide gel electrophoresis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2800%2901510-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The ubiquitin pathway in Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2800%2901510-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Low frequency of pathogenic mutations in the ubiquitin carboxy-terminal hydrolase gene in familial Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2800%2901510-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ubiquitin conjugate immunoreactivity in the brains of scrapie infected mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2800%2901510-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Case-control study of the ubiquitin carboxy-terminal hydrolase L1 gene in Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2800%2901510-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The monoamine oxidase B gene GT repeat polymorphism and Parkinson's disease in a Chinese population
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2800%2901510-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Q64854089
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2800%2901510-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2800%2901510-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Intragenic deletion in the gene encoding ubiquitin carboxy-terminal hydrolase in gad mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2800%2901510-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2800%2901510-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0304-3940(00)01510-X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11027850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11027850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
PubMed publication ID
11027850
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11027850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11027850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
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