(Q22252835)

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613245

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613245

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613245

Age-dependent motor deficits and dopaminergic dysfunction in DJ-1 null mice

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613245

Nigrostriatal dopaminergic deficits and hypokinesia caused by inactivation of the familial Parkinsonism-linked gene DJ-1

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613245

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613245

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613245

Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613245

Parkinson's disease: mechanisms and models

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613245

High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613245

Progressive parkinsonism in mice with respiratory-chain-deficient dopamine neurons

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613245

Novel PINK1 mutations in early-onset parkinsonism

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613245

DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613245

Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613245

The role of pathogenic DJ-1 mutations in Parkinson's disease.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613245

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

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613245

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

29 November 2018

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Distribution, type, and origin of Parkin mutations: review and case studies

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

The importance of gene dosage studies: mutational analysis of the parkin gene in early-onset parkinsonism

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

An unfolded putative transmembrane polypeptide, which can lead to endoplasmic reticulum stress, is a substrate of Parkin

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Parkin gene inactivation alters behaviour and dopamine neurotransmission in the mouse

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Hypersensitivity of DJ-1-deficient mice to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyrindine (MPTP) and oxidative stress.

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Impaired dopamine release and synaptic plasticity in the striatum of PINK1-deficient mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Deciphering the role of heterozygous mutations in genes associated with parkinsonism

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Association between early-onset Parkinson's disease and mutations in the parkin gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Parkin mutations and susceptibility alleles in late-onset Parkinson's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Mitochondrial dysfunction and oxidative damage in parkin-deficient mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Parkin-deficient mice are not more sensitive to 6-hydroxydopamine or methamphetamine neurotoxicity

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Parkin-deficient mice are not a robust model of parkinsonism

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Parkin mutations are frequent in patients with isolated early-onset parkinsonism.

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

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

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Decline of striatal dopamine release in parkin-deficient mice shown by ex vivo autoradiography.

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Mitochondria and dopamine: new insights into recessive parkinsonism

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

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

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

PINK1 mutations in sporadic early-onset Parkinson's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Association of PINK1 and DJ-1 confers digenic inheritance of early-onset Parkinson's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

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

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

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

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36.

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Loss of locus coeruleus neurons and reduced startle in parkin null mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

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

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15

Silencing of the Pink1 gene expression by conditional RNAi does not induce dopaminergic neuron death in mice.

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-78205-7_15