(Q36611513)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17017528%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

review article

1 reference

title

Genetic causes of Parkinson's disease: extending the pathway (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17017528%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

1 reference

O Riess

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17017528%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

R Krüger

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17017528%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

H Hochstrasser

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17017528%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

A S Soehn

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17017528%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

S Nuber

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17017528%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

T Franck

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17017528%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

D Berg

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17017528%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

publication date

1 January 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17017528%20AND%20SRC:MED&resulttype=core&format=json

Journal of neural transmission. Supplementum

20 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17017528%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

issue

70

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17017528%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

page(s)

181-189

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17017528%20AND%20SRC:MED&resulttype=core&format=json

Synphilin-1 and parkin show overlapping expression patterns in human brain and form aggresomes in response to proteasomal inhibition

20 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Energetics in the pathogenesis of neurodegenerative diseases

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Mutations in PTEN-induced putative kinase 1 associated with recessive parkinsonism have differential effects on protein stability

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Echogenicity of the substantia nigra: association with increased iron content and marker for susceptibility to nigrostriatal injury

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

14-3-3 proteins in the nervous system

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Specification of 14-3-3 proteins in Lewy bodies

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Anemia and iron overload due to compound heterozygosity for novel ceruloplasmin mutations.

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

The Parkinson's disease protein DJ-1 is neuroprotective due to cysteine-sulfinic acid-driven mitochondrial localization

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Parkin ubiquitinates the alpha-synuclein-interacting protein, synphilin-1: implications for Lewy-body formation in Parkinson disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Screening for mutations of the IRP2 gene in Parkinson's disease patients with hyperechogenicity of the substantia nigra.

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Synphilin-1 associates with alpha-synuclein and promotes the formation of cytosolic inclusions

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

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

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Screening for mutations of the ferritin light and heavy genes in Parkinson's disease patients with hyperechogenicity of the substantia nigra

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

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

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

The parkinsonian neurotoxin, MPP+ induces phosphorylated c-Jun in dopaminergric neurons of mesencephalic cultures

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Mutant and wild type human alpha-synucleins assemble into elongated filaments with distinct morphologies in vitro

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Parkin-deficient mice exhibit nigrostriatal deficits but not loss of dopaminergic neurons

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Mitochondrial pathology and apoptotic muscle degeneration in Drosophila parkin mutants

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

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

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Roles of N-linked glycans in the endoplasmic reticulum

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

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

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Ceruloplasmin gene variations and substantia nigra hyperechogenicity in Parkinson disease.

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Functional relevance of ceruloplasmin mutations in Parkinson's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Noncanonical MMS2-encoded ubiquitin-conjugating enzyme functions in assembly of novel polyubiquitin chains for DNA repair

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Parkin gene inactivation alters behaviour and dopamine neurotransmission in the mouse

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

14-3-3 proteins in Lewy bodies in Parkinson disease and diffuse Lewy body disease brains

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Expression of the ceruloplasmin gene in the human retina and brain: implications for a pathogenic model in aceruloplasminemia

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Aceruloplasminemia with a novel mutation associated with parkinsonism

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotype

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Sustained extracellular signal-regulated kinase activation by 6-hydroxydopamine: implications for Parkinson's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Targeted deletion of the gene encoding iron regulatory protein-2 causes misregulation of iron metabolism and neurodegenerative disease in mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Casein kinase II-mediated phosphorylation regulates alpha-synuclein/synphilin-1 interaction and inclusion body formation

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

The ubiquitin pathway in Parkinson's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Ubiquitylation of synphilin-1 and alpha-synuclein by SIAH and its presence in cellular inclusions and Lewy bodies imply a role in Parkinson's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

The UCH-L1 gene encodes two opposing enzymatic activities that affect alpha-synuclein degradation and Parkinson's disease susceptibility

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Mitochondrial dysfunction and oxidative damage in parkin-deficient mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Significant linkage of Parkinson disease to chromosome 2q36-37

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Drosophila parkin mutants have decreased mass and cell size and increased sensitivity to oxygen radical stress

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Echogenicity of the substantia nigra in relatives of patients with sporadic Parkinson's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Mitochondrial involvement in Parkinson's disease, Huntington's disease, hereditary spastic paraplegia and Friedreich's ataxia

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Protein kinases linked to the pathogenesis of Parkinson's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

alpha-Synuclein locus triplication causes Parkinson's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Alpha-synuclein in Lewy bodies

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

DJ-1 has a role in antioxidative stress to prevent cell death

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Polymorphism of NACP-Rep1 in Parkinson's disease: an etiologic link with essential tremor?

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Mouse brains deficient in H-ferritin have normal iron concentration but a protein profile of iron deficiency and increased evidence of oxidative stress.

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Regulation of tyrosine hydroxylase by stress-activated protein kinases

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Human and mouse alpha-synuclein genes: comparative genomic sequence analysis and identification of a novel gene regulatory element

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

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

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Overexpression of alpha-synuclein in rat substantia nigra results in loss of dopaminergic neurons, phosphorylation of alpha-synuclein and activation of caspase-9: resemblance to pathogenetic changes in Parkinson's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Parkin phosphorylation and modulation of its E3 ubiquitin ligase activity

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_29

10.1007/978-3-211-45295-0_29

31 March 2020

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17017528%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

1 reference