(Q28507691)

24 January 2017

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10 January 2020

title

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

2 references

24 January 2017

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Parkinson disease (autosomal recessive, early onset) 7

10 January 2020

main subject

1 reference

GOA release 2020-03-11

1 reference

4

1 reference

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10 January 2020

author name string

Linan Chen

1

2 references

24 January 2017

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10 January 2020

Barbara Cagniard

2

2 references

24 January 2017

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10 January 2020

Tiffany Mathews

3

2 references

24 January 2017

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10 January 2020

Hyun Chul Koh

5

2 references

24 January 2017

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10 January 2020

Yunmin Ding

6

2 references

24 January 2017

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10 January 2020

Zaodung Ling

8

2 references

24 January 2017

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10 January 2020

Un Jung Kang

9

2 references

24 January 2017

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10 January 2020

Xiaoxi Zhuang

10

2 references

24 January 2017

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10 January 2020

Paul M Carvey

7

1 reference

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10 January 2020

language of work or name

English

0 references

publication date

30 March 2005

1 reference

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Journal of Biological Chemistry

10 January 2020

published in

2 references

24 January 2017

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10 January 2020

volume

280

2 references

24 January 2017

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10 January 2020

issue

22

2 references

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10 January 2020

page(s)

21418-21426

1 reference

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

10 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M413955200

L166P mutant DJ-1, causative for recessive Parkinson's disease, is degraded through the ubiquitin-proteasome system

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M413955200

The DJ-1L166P mutant protein associated with early onset Parkinson's disease is unstable and forms higher-order protein complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M413955200

Familial Parkinson's disease-associated L166P mutation disrupts DJ-1 protein folding and function

21 January 2018

1 reference

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

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

https://api.crossref.org/works/10.1074%2FJBC.M413955200

Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7).

21 January 2018

1 reference

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Differential Effects of Parkinson's Disease-associated Mutations on Stability and Folding of DJ-1

21 January 2018

1 reference

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DJ-1, a novel oncogene which transforms mouse NIH3T3 cells in cooperation with ras

21 January 2018

1 reference

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DJ-1, a target protein for an endocrine disrupter, participates in the fertilization in mice

21 January 2018

1 reference

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DJ-1 positively regulates the androgen receptor by impairing the binding of PIASx alpha to the receptor

21 January 2018

1 reference

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Oxidized forms of peroxiredoxins and DJ-1 on two-dimensional gels increased in response to sublethal levels of paraquat

21 January 2018

1 reference

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DJ-1 is an indicator for endogenous reactive oxygen species elicited by endotoxin

21 January 2018

1 reference

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Reduced anti-oxidative stress activities of DJ-1 mutants found in Parkinson's disease patients

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M413955200

Sensitivity to oxidative stress in DJ-1-deficient dopamine neurons: an ES- derived cell model of primary Parkinsonism

21 January 2018

1 reference

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

21 January 2018

1 reference

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The 1.1-A resolution crystal structure of DJ-1, the protein mutated in autosomal recessive early onset Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M413955200

Crystal structure of human DJ-1, a protein associated with early onset Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M413955200

Crystal structures of human DJ-1 and Escherichia coli Hsp31, which share an evolutionarily conserved domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M413955200

Crystal structure of DJ-1/RS and implication on familial Parkinson's disease

21 January 2018

1 reference

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The crystal structure of DJ-1, a protein related to male fertility and Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M413955200

DJ-1 is a redox-dependent molecular chaperone that inhibits alpha-synuclein aggregate formation

21 January 2018

1 reference

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Presynaptic dopaminergic function is largely unaltered in mesolimbic and mesostriatal terminals of adult rats that were prenatally exposed to cocaine

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M413955200

Localization of DJ-1 mRNA in the mouse brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M413955200

The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M413955200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M413955200

Early and progressive sensorimotor anomalies in mice overexpressing wild-type human alpha-synuclein.

21 January 2018

1 reference

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Ubiquitin is a common factor in intermediate filament inclusion bodies of diverse type in man, including those of Parkinson's disease, Pick's disease, and Alzheimer's disease, as well as Rosenthal fibres in cerebellar astrocytomas, cytoplasmic bodie

21 January 2018

1 reference

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Pathoanatomy of Parkinson's disease

21 January 2018

1 reference

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α-Synuclein in Lewy bodies

21 January 2018

1 reference

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Ubiquitin is associated with abnormal cytoplasmic filaments characteristic of neurodegenerative diseases

21 January 2018

1 reference

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The "staircase test": a measure of independent forelimb reaching and grasping abilities in rats

21 January 2018

1 reference

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Effects of complete and partial lesions of the dopaminergic mesotelencephalic system on skilled forelimb use in the rat

21 January 2018

1 reference

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Biochemical and anatomical characterization of forepaw adjusting steps in rat models of Parkinson's disease: studies on medial forebrain bundle and striatal lesions

21 January 2018

1 reference

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The hyperpolarization-activated HCN1 channel is important for motor learning and neuronal integration by cerebellar Purkinje cells

21 January 2018

1 reference

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Hyperactivity and impaired response habituation in hyperdopaminergic mice

21 January 2018

1 reference

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Hyperlocomotion and indifference to cocaine and amphetamine in mice lacking the dopamine transporter

21 January 2018

1 reference

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Profound neuronal plasticity in response to inactivation of the dopamine transporter

21 January 2018

1 reference

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Role of oxidation in the neurotoxic effects of intrastriatal dopamine injections

21 January 2018

1 reference

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Dopamine toxicity involves mitochondrial complex I inhibition: implications to dopamine-related neuropsychiatric disorders

21 January 2018

1 reference

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Dopamine toxicity in neuroblastoma cells: role of glutathione depletion by L-BSO and apoptosis

21 January 2018

1 reference

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Neurotoxin-induced degeneration of dopamine neurons in Caenorhabditis elegans

21 January 2018

1 reference

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Oligomerization and trafficking of the human dopamine transporter. Mutational analysis identifies critical domains important for the functional expression of the transporter

21 January 2018

1 reference

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Functional interaction between monoamine plasma membrane transporters and the synaptic PDZ domain-containing protein PICK1

21 January 2018

1 reference

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Incidence of Parkinson's disease: variation by age, gender, and race/ethnicity

21 January 2018

1 reference

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Alteration of intracellular structure and function of glyceraldehyde-3-phosphate dehydrogenase: a common phenotype of neurodegenerative disorders?

21 January 2018

1 reference

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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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21 January 2018

Identifiers

DOI

10.1074/JBC.M413955200

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15799973%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

1 reference

Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017