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Genetics and genomics of Parkinson's disease
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
4085542
retrieved
31 August 2017
title
Genetics and genomics of Parkinson's disease
(English)
1 reference
stated in
Europe PubMed Central
PMCID
4085542
retrieved
31 August 2017
main subject
Parkinson's disease
1 reference
based on heuristic
inferred from title
genomics
0 references
author
Matthew J. Farrer
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
4085542
retrieved
31 August 2017
author name string
Michelle K Lin
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
4085542
retrieved
31 August 2017
language of work or name
English
1 reference
based on heuristic
inferred from title
publication date
30 June 2014
1 reference
stated in
Europe PubMed Central
PMCID
4085542
retrieved
31 August 2017
published in
Genome Medicine
1 reference
stated in
Europe PubMed Central
PMCID
4085542
retrieved
31 August 2017
volume
6
1 reference
stated in
Europe PubMed Central
PMCID
4085542
retrieved
31 August 2017
issue
6
1 reference
stated in
Europe PubMed Central
PMCID
4085542
retrieved
31 August 2017
page(s)
48
1 reference
stated in
Europe PubMed Central
PMCID
4085542
retrieved
31 August 2017
exact match
https://scigraph.springernature.com/pub.10.1186/gm566
0 references
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Mutant LRRK2 enhances glutamatergic synapse activity and evokes excitotoxic dendrite degeneration
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6 September 2017
Ubiquitin is phosphorylated by PINK1 to activate parkin
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6 September 2017
LRRK2 regulates synaptogenesis and dopamine receptor activation through modulation of PKA activity
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6 September 2017
Functional interaction of Parkinson's disease-associated LRRK2 with members of the dynamin GTPase superfamily
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6 September 2017
DNAJC13 mutations in Parkinson disease
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6 September 2017
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6 September 2017
Hexokinase activity is required for recruitment of parkin to depolarized mitochondria
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6 September 2017
The Parkinson's disease-linked proteins Fbxo7 and Parkin interact to mediate mitophagy
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6 September 2017
Advances in the genetics of Parkinson disease
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6 September 2017
The Sac1 domain of SYNJ1 identified mutated in a family with early-onset progressive Parkinsonism with generalized seizures
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6 September 2017
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
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6 September 2017
Retromer-mediated endosomal protein sorting: all WASHed up!
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6 September 2017
Structure of parkin reveals mechanisms for ubiquitin ligase activation
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6 September 2017
Signals from the lysosome: a control centre for cellular clearance and energy metabolism
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6 September 2017
Altered splicing of ATP6AP2 causes X-linked parkinsonism with spasticity (XPDS).
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6 September 2017
Behavioral and metabolic characterization of heterozygous and homozygous POLG mutator mice
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6 September 2017
Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease
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6 September 2017
RAB7L1 interacts with LRRK2 to modify intraneuronal protein sorting and Parkinson's disease risk
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PubMed Central
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6 September 2017
Atp13a2-deficient mice exhibit neuronal ceroid lipofuscinosis, limited α-synuclein accumulation and age-dependent sensorimotor deficits
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6 September 2017
Mapping the subcellular distribution of α-synuclein in neurons using genetically encoded probes for correlated light and electron microscopy: implications for Parkinson's disease pathogenesis
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6 September 2017
Obstacles to the development of a neuroprotective therapy for Parkinson's disease
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6 September 2017
Immunotherapy for neurodegenerative diseases: focus on α-synucleinopathies
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6 September 2017
Endosomal recruitment of the WASH complex: active sequences and mutations impairing interaction with the retromer
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PubMed Central
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6 September 2017
Phenotypic impact of genomic structural variation: insights from and for human disease
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6 September 2017
Augmenting CNS glucocerebrosidase activity as a therapeutic strategy for parkinsonism and other Gaucher-related synucleinopathies
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6 September 2017
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6 September 2017
Monomeric synucleins generate membrane curvature
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6 September 2017
Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA.
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6 September 2017
Pathological α-synuclein transmission initiates Parkinson-like neurodegeneration in nontransgenic mice
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6 September 2017
LRRK2 controls an EndoA phosphorylation cycle in synaptic endocytosis
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6 September 2017
An emerging role for LRRK2 in the immune system
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6 September 2017
ROS-dependent regulation of Parkin and DJ-1 localization during oxidative stress in neurons.
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6 September 2017
Pharmacological rescue of mitochondrial deficits in iPSC-derived neural cells from patients with familial Parkinson's disease
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6 September 2017
Evolution and functional impact of rare coding variation from deep sequencing of human exomes
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6 September 2017
A deleterious mutation in DNAJC6 encoding the neuronal-specific clathrin-uncoating co-chaperone auxilin, is associated with juvenile parkinsonism
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6 September 2017
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database
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6 September 2017
Statistical guidance for experimental design and data analysis of mutation detection in rare monogenic mendelian diseases by exome sequencing
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6 September 2017
LRRK2 regulates mitochondrial dynamics and function through direct interaction with DLP1
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6 September 2017
Translation initiator EIF4G1 mutations in familial Parkinson disease
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6 September 2017
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study
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6 September 2017
α-Synuclein occurs physiologically as a helically folded tetramer that resists aggregation
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6 September 2017
LRRK2 protein levels are determined by kinase function and are crucial for kidney and lung homeostasis in mice
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6 September 2017
A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease
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6 September 2017
VPS35 mutations in Parkinson disease
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6 September 2017
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease
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6 September 2017
The curious case of phenocopies in families with genetic Parkinson's disease
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6 September 2017
Gaucher disease glucocerebrosidase and α-synuclein form a bidirectional pathogenic loop in synucleinopathies
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6 September 2017
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
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6 September 2017
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6 September 2017
Heritability of Parkinson disease in Swedish twins: a longitudinal study
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6 September 2017
Characterization of a selective inhibitor of the Parkinson's disease kinase LRRK2.
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6 September 2017
PARIS (ZNF746) repression of PGC-1α contributes to neurodegeneration in Parkinson's disease
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6 September 2017
Meta-analysis of published studies identified eight additional common susceptibility loci for Crohn's disease and ulcerative colitis
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6 September 2017
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
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6 September 2017
Genome-wide association study confirms extant PD risk loci among the Dutch
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6 September 2017
Adult neurogenesis and neurite outgrowth are impaired in LRRK2 G2019S mice
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6 September 2017
LRRK2 is involved in the IFN-gamma response and host response to pathogens
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6 September 2017
A comparative study of Lrrk2 function in primary neuronal cultures
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6 September 2017
Alpha-synuclein promotes SNARE-complex assembly in vivo and in vitro
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6 September 2017
Alpha-synuclein suppression by targeted small interfering RNA in the primate substantia nigra
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6 September 2017
Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease
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6 September 2017
Disentangling the role of the tau gene locus in sporadic tauopathies
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6 September 2017
Inhibition of LRRK2 kinase activity leads to dephosphorylation of Ser(910)/Ser(935), disruption of 14-3-3 binding and altered cytoplasmic localization
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6 September 2017
The epidemiology of dementia associated with Parkinson's disease
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6 September 2017
The mitochondrial fusion-promoting factor mitofusin is a substrate of the PINK1/parkin pathway
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6 September 2017
alpha-synuclein and LRRK2: partners in crime
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6 September 2017
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
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6 September 2017
Genome-wide association study reveals genetic risk underlying Parkinson's disease
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PubMed Central
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6 September 2017
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.
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6 September 2017
The LRRK2 G2019S mutation as the cause of Parkinson's disease in Ashkenazi Jews
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6 September 2017
Targeted capture and massively parallel sequencing of 12 human exomes
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6 September 2017
Is Parkinson's disease a prion disorder?
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6 September 2017
Parkinson phenotype in aged PINK1-deficient mice is accompanied by progressive mitochondrial dysfunction in absence of neurodegeneration
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=4085542
retrieved
6 September 2017
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
1 reference
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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=4085542
retrieved
6 September 2017
Common genetic variation and human traits
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=4085542
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6 September 2017
Evolutionary toggling of the MAPT 17q21.31 inversion region
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=4085542
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6 September 2017
Clinical and molecular features of mitochondrial DNA depletion syndromes.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4085542
retrieved
6 September 2017
Deep brain stimulation of the subthalamic nucleus for the treatment of Parkinson's disease
1 reference
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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=4085542
retrieved
6 September 2017
FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome
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=4085542
retrieved
6 September 2017
Emerging pathways in genetic Parkinson's disease: Potential role of ceramide metabolism in Lewy body disease
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=4085542
retrieved
6 September 2017
Genomewide association study for susceptibility genes contributing to familial Parkinson disease
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=4085542
retrieved
6 September 2017
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome
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=4085542
retrieved
6 September 2017
Genomic investigation of alpha-synuclein multiplication and parkinsonism
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=4085542
retrieved
6 September 2017
Characterization of PLA2G6 as a locus for dystonia-parkinsonism
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=4085542
retrieved
6 September 2017
LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study
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=4085542
retrieved
6 September 2017
The Roco protein family: a functional perspective
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=4085542
retrieved
6 September 2017
Lewy body-like pathology in long-term embryonic nigral transplants in Parkinson's disease
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=4085542
retrieved
6 September 2017
LRRK2 phosphorylates moesin at threonine-558: characterization of how Parkinson's disease mutants affect kinase activity
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=4085542
retrieved
6 September 2017
Identification of a novel mitochondrial complex containing mitofusin 2 and stomatin-like protein 2
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=4085542
retrieved
6 September 2017
The familial Parkinsonism gene LRRK2 regulates neurite process morphology
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=4085542
retrieved
6 September 2017
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data
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=4085542
retrieved
6 September 2017
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
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=4085542
retrieved
6 September 2017
Epidemiology of Parkinson's disease
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=4085542
retrieved
6 September 2017
Parkinson's disease brain mitochondrial complex I has oxidatively damaged subunits and is functionally impaired and misassembled.
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=4085542
retrieved
6 September 2017
Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin
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=4085542
retrieved
6 September 2017
Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin
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=4085542
retrieved
6 September 2017
The Parkinson's complex: parkinsonism is just the tip of the iceberg
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=4085542
retrieved
6 September 2017
Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity
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=4085542
retrieved
6 September 2017
High-resolution whole-genome association study of Parkinson disease.
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=4085542
retrieved
6 September 2017
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations
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=4085542
retrieved
6 September 2017
Nigrostriatal dopaminergic deficits and hypokinesia caused by inactivation of the familial Parkinsonism-linked gene DJ-1
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=4085542
retrieved
6 September 2017
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
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=4085542
retrieved
6 September 2017
Alpha-synuclein locus duplication as a cause of familial Parkinson's disease
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=4085542
retrieved
6 September 2017
Novel PINK1 mutations in early-onset parkinsonism
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=4085542
retrieved
6 September 2017
Linkage disequilibrium and association of MAPT H1 in Parkinson disease
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=4085542
retrieved
6 September 2017
Hereditary early-onset Parkinson's disease caused by mutations in PINK1
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=4085542
retrieved
6 September 2017
Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications
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=4085542
retrieved
6 September 2017
alpha-Synuclein locus triplication causes Parkinson's disease
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=4085542
retrieved
6 September 2017
Parkin-deficient mice exhibit nigrostriatal deficits but not loss of dopaminergic neurons
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=4085542
retrieved
6 September 2017
Description of Parkinson's disease as a clinical syndrome.
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=4085542
retrieved
6 September 2017
Parkin is a component of an SCF-like ubiquitin ligase complex and protects postmitotic neurons from kainate excitotoxicity
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=4085542
retrieved
6 September 2017
Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism
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=4085542
retrieved
6 September 2017
The accuracy of diagnosis of parkinsonian syndromes in a specialist movement disorder service
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=4085542
retrieved
6 September 2017
Lewy bodies and parkinsonism in families with parkin mutations
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=4085542
retrieved
6 September 2017
Mice lacking alpha-synuclein display functional deficits in the nigrostriatal dopamine system
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=4085542
retrieved
6 September 2017
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease
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=4085542
retrieved
6 September 2017
Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17
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=4085542
retrieved
6 September 2017
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
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=4085542
retrieved
6 September 2017
Alpha-synuclein in Lewy bodies
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=4085542
retrieved
6 September 2017
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
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=4085542
retrieved
6 September 2017
Chronic Parkinsonism in humans due to a product of meperidine-analog synthesis
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=4085542
retrieved
6 September 2017
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
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=4085542
retrieved
6 September 2017
Retromer mediates a discrete route of local membrane delivery to dendrites
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=4085542
retrieved
14 September 2017
Expanding the clinical phenotype of SNCA duplication carriers
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=4085542
retrieved
14 September 2017
Assembly-dependent endocytosis and clearance of extracellular alpha-synuclein.
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=4085542
retrieved
14 September 2017
Parkinsonism, Lrrk2 G2019S, and tau neuropathology
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=4085542
retrieved
14 September 2017
A regulated interaction with the UIM protein Eps15 implicates parkin in EGF receptor trafficking and PI(3)K-Akt signalling
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=4085542
retrieved
14 September 2017
Accumulation of the authentic parkin substrate aminoacyl-tRNA synthetase cofactor, p38/JTV-1, leads to catecholaminergic cell death.
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=4085542
retrieved
14 September 2017
PINK1-Interacting Proteins: Proteomic Analysis of Overexpressed PINK1.
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=4085542
retrieved
23 June 2018
Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations.
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=4085542
retrieved
23 June 2018
Comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p.G2019S parkinsonism
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=4085542
retrieved
31 August 2018
100 years of Lewy pathology.
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=4085542
retrieved
31 August 2018
VPS35 mutation in Japanese patients with typical Parkinson's disease.
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=4085542
retrieved
31 August 2018
LRRK2 I2020T mutation is associated with tau pathology.
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=4085542
retrieved
31 August 2018
Optical reporters for the conformation of alpha-synuclein reveal a specific interaction with mitochondria
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=4085542
retrieved
31 August 2018
LRK-1, a C. elegans PARK8-related kinase, regulates axonal-dendritic polarity of SV proteins
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=4085542
retrieved
31 August 2018
Leucine-rich repeat kinase 2 G2385R variant is a risk factor for Parkinson disease in Asian population.
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=4085542
retrieved
31 August 2018
Frequency of LRRK2 mutations in early- and late-onset Parkinson disease.
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=4085542
retrieved
31 August 2018
Lrrk2 and Lewy body disease
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=4085542
retrieved
31 August 2018
LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.
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=4085542
retrieved
31 August 2018
Parkinson's disease alpha-synuclein transgenic mice develop neuronal mitochondrial degeneration and cell death.
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=4085542
retrieved
31 August 2018
Multiple roles for cyclin G-associated kinase in clathrin-mediated sorting events
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=4085542
retrieved
31 August 2018
The tau locus is not significantly associated with pathologically confirmed sporadic Parkinson's disease.
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=4085542
retrieved
31 August 2018
Causal relation between alpha-synuclein gene duplication and familial Parkinson's disease
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/25061481
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
alpha-synuclein gene haplotypes are associated with Parkinson's disease
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/25061481
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identification of VPS35 mutations replicated in French families with Parkinson disease
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/25061481
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Regulation of clathrin-dependent endocytosis by diacylglycerol kinase delta: importance of kinase activity and binding to AP2alpha
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/25061481
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotype
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/25061481
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Case-control study of the extended tau gene haplotype in Parkinson's disease
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/25061481
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1186/GM566
1 reference
stated in
Europe PubMed Central
PMCID
4085542
retrieved
31 August 2017
Dimensions Publication ID
1033897639
0 references
PMCID
4085542
1 reference
stated in
Europe PubMed Central
PMCID
4085542
retrieved
31 August 2017
PubMed ID
25061481
1 reference
stated in
Europe PubMed Central
PMCID
4085542
retrieved
31 August 2017
ResearchGate publication ID
264247824
0 references
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