(Q58269122)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16026116%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

review article

1 reference

title

Genetics of Parkinson's disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16026116%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16026116%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

author name string

Huw R. Morris

series ordinal

1

0 references

language of work or name

English

0 references

publication date

1 January 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16026116%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16026116%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

volume

37

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16026116%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

page(s)

86-96

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16026116%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16026116%20AND%20SRC:MED&resulttype=core&format=json

beta-peptide immunization: a possible new treatment for Alzheimer disease

31 December 2019

cites work

1 reference

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PINK, PANK, or PARK? A clinicians' guide to familial parkinsonism

21 January 2018

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Impact of genetic analysis on Parkinson's disease research

21 January 2018

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21 January 2018

Genetics of parkinsonism

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Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases

21 January 2018

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Chronic parkinsonism secondary to intravenous injection of meperidine analogues

21 January 2018

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Familial aggregation of Parkinson's disease: The Mayo Clinic family study

21 January 2018

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Familial aggregation of Parkinson disease: a comparative study of early-onset and late-onset disease

21 January 2018

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Familial Aggregation of Parkinson's Disease in Iceland

21 January 2018

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A large kindred with autosomal dominant Parkinson's disease

21 January 2018

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Clinical genetic analysis of Parkinson's disease in the Contursi kindred

21 January 2018

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Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

21 January 2018

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Familial parkinsonism with synuclein pathology: clinical and PET studies of A30P mutation carriers.

21 January 2018

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alpha-Synuclein locus triplication causes Parkinson's disease

21 January 2018

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Low frequency of alpha-synuclein mutations in familial Parkinson's disease.

21 January 2018

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Alpha-synuclein in Lewy bodies

21 January 2018

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Alpha-synuclein and neurodegenerative diseases

21 January 2018

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Association between cardiac denervation and parkinsonism caused by alpha-synuclein gene triplication

21 January 2018

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Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications

21 January 2018

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A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1.

21 January 2018

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The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval

21 January 2018

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Autosomal dominant parkinsonism associated with variable synuclein and tau pathology.

21 January 2018

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Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic study

21 January 2018

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Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

21 January 2018

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A susceptibility locus for Parkinson's disease maps to chromosome 2p13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007269

Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007269

A haplotype at the PARK3 locus influences onset age for Parkinson's disease: the GenePD study

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007269

The ubiquitin pathway in Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007269

Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007269

Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007269

A susceptibility gene for late-onset idiopathic Parkinson's disease

21 January 2018

1 reference

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Significant linkage of Parkinson disease to chromosome 2q36-37

21 January 2018

1 reference

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Young-onset Parkinson's disease: a clinical review

21 January 2018

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Familial juvenile parkinsonism: clinical and pathologic study in a family.

21 January 2018

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A microdeletion of D6S305 in a family of autosomal recessive juvenile parkinsonism (PARK2).

21 January 2018

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Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

21 January 2018

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Genetics of parkin-linked disease.

21 January 2018

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Pathogenetic mechanisms of parkin in Parkinson's disease

21 January 2018

1 reference

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Parkin-associated Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007269

Parkin functions as an E2-dependent ubiquitin- protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007269

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007269

The ubiquitin-proteasome proteolytic pathway: destruction for the sake of construction

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007269

Ubiquitination of a new form of alpha-synuclein by parkin from human brain: implications for Parkinson's disease

21 January 2018

1 reference

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Pael-R is accumulated in Lewy bodies of Parkinson's disease.

21 January 2018

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Parkin protects against the toxicity associated with mutant alpha-synuclein: proteasome dysfunction selectively affects catecholaminergic neurons

21 January 2018

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Parkin disease: a phenotypic study of a large case series

21 January 2018

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Lewy bodies and parkinsonism in families with parkin mutations

21 January 2018

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Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations.

21 January 2018

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Tau gene and Parkinson's disease: a case-control study and meta-analysis

21 January 2018

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Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation

21 January 2018

1 reference

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DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease.

21 January 2018

1 reference

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Association of DJ-1 and parkin mediated by pathogenic DJ-1 mutations and oxidative stress

21 January 2018

1 reference

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Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36

21 January 2018

1 reference

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PINK1 mutations are associated with sporadic early-onset parkinsonism

21 January 2018

1 reference

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Hereditary early-onset Parkinson's disease caused by mutations in PINK1

21 January 2018

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Novel PINK1 mutations in early-onset parkinsonism

21 January 2018

1 reference

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PINK1 (PARK6) associated Parkinson disease in Ireland

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007269

Homozygous PINK1 C-terminus mutation causing early-onset parkinsonism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007269

Complex relationship between Parkin mutations and Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007269

Progression of nigrostriatal dysfunction in a parkin kindred: an [18F]dopa PET and clinical study

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007269

SCA2 may present as levodopa-responsive parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007269

Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007269

Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007269

Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007269

10.1080/07853890510007269

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16026116%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

1 reference