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English
Genetics of Parkinson's disease
scientific article published on 01 April 1999
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10349506
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10349506%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
review article
1 reference
stated in
Europe PubMed Central
title
Genetics of Parkinson's disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10349506
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10349506%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
main subject
Parkinson's disease
1 reference
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inferred from title
author name string
Y Mizuno
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10349506
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10349506%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
N Hattori
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10349506
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10349506%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
H Mori
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10349506
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10349506%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
publication date
1 April 1999
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10349506
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10349506%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
published in
Biomedicine and Pharmacotherapy
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10349506
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10349506%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
volume
53
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10349506
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10349506%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10349506
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10349506%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
page(s)
109-116
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10349506
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10349506%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
cites work
Human BAC library: construction and rapid screening
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7 January 2021
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Familial parkinsonism with depression: a clinicopathological study
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Crossref
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7 January 2021
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The human NACP/α-synuclein gene: chromosome assignment to 4q21.3–q22 and TaqI RFLP analysis
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7 January 2021
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Sublocalization of the gene encoding manganese superoxide dismutase (MnSOD/SOD2) to 6q25 by fluorescence in situ hybridization and somatic cell hybrid mapping
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Crossref
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7 January 2021
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Familial parkinsonism: Our experience and review
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Crossref
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7 January 2021
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Familial parkinsonism, dementia, and Lewy body disease: study of family G.
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reference URL
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7 January 2021
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Dominantly inherited, early-onset parkinsonism: neuropathology of a new form
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7 January 2021
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A susceptibility locus for Parkinson's disease maps to chromosome 2p13.
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7 January 2021
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A large kindred with autosomal dominant Parkinson's disease
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical genetic analysis of Parkinson's disease in the Contursi kindred
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
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7 January 2021
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Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin gene
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular genetic analysis of a novelParkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in theParkin gene in affected individuals
1 reference
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Crossref
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7 January 2021
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inferred from DOI database lookup
Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17
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7 January 2021
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inferred from DOI database lookup
Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonism.
1 reference
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Crossref
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7 January 2021
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The precursor protein of non-A beta component of Alzheimer's disease amyloid is a presynaptic protein of the central nervous system
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
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7 January 2021
based on heuristic
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Autosomal recessive juvenile parkinsonism maps to 6q25.2-q27 in four ethnic groups: detailed genetic mapping of the linked region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Lewy bodies in cerebral cortex, report of three cases
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
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7 January 2021
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inferred from DOI database lookup
Substrate specificity of deubiquitinating enzymes: ubiquitin C-terminal hydrolases
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
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7 January 2021
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inferred from DOI database lookup
The ubiquitin pathway in Parkinson's disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex.
1 reference
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Crossref
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7 January 2021
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inferred from DOI database lookup
Structure, microtubule interactions, and phosphorylation of tau protein
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Synuclein: a neuron-specific protein localized to the nucleus and presynaptic nerve terminal
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
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7 January 2021
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inferred from DOI database lookup
The rat brain synucleins; family of proteins transiently associated with neuronal membrane
1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
Early onset parkinsonism with diurnal fluctuation maps to a locus for juvenile parkinsonism
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Neurochemical and neurogenetic correlates of Parkinson's disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Familial autosomal dominant dopa responsive Parkinson's disease in three living generations showing extreme anticipation and childhood onset
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary form of parkinsonism--dementia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Dominantly inherited apathy, central hypoventilation, and Parkinson's syndrome: clinical, biochemical, and neuropathologic studies of 2 new cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mapping of a gene for Parkinson's disease to chromosome 4q21-q23
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
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%2FS0753-3322%2899%2980075-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tau is a candidate gene for chromosome 17 frontotemporal dementia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parkinsonism and neurofibrillary tangle pathology in pigmented nuclei.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The neuropathology of a chromosome 17-linked autosomal dominant parkinsonism and dementia ("pallido-ponto-nigral degeneration").
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structural dimorphism in the mitochondrial targeting sequence in the human manganese superoxide dismutase gene. A predictive evidence for conformational change to influence mitochondrial transport and a study of allelic association in Parkinson's di
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Immunohistochemical and subcellular localization of Parkin protein: absence of protein in autosomal recessive juvenile parkinsonism patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Report of familial cases of parkinsonism. Evidence of a dominant trait in a patient's family.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assignment of human alpha-synuclein (SNCA) and beta-synuclein (SNCB) genes to chromosomes 4q21 and 5q35.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
α-Synuclein in Lewy bodies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial juvenile parkinsonism: clinical and pathologic study in a family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
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%2FS0753-3322%2899%2980075-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
NACP, a presynaptic protein, immunoreactivity in Lewy bodies in Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal dominant Lewy body parkinsonism in a four-generation family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Western Nebraska family (family D) with autosomal dominant parkinsonism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
German-Canadian family (family A) with parkinsonism, amyotrophy, and dementia - Longitudinal observations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Paralysis agitans of early onset with marked diurnal fluctuation of symptoms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical, pathologic and genetic studies on autosomal recessive early-onset parkinsonism with diurnal fluctuation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980075-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0753-3322(99)80075-4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10349506
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10349506%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
PubMed publication ID
10349506
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10349506
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10349506%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
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