Complex I deficiency and dopaminergic neuronal cell loss in parkin-deficient zebrafish (Danio rerio). (Q39979942)

16 September 2017

title

Complex I deficiency and dopaminergic neuronal cell loss in parkin-deficient zebrafish (Danio rerio). (English)

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16 September 2017

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16 September 2017

Heather Mortiboys

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Oliver Bandmann

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Laura Flinn

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16 September 2017

Katrin Volkmann

series ordinal

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16 September 2017

Reinhard W Köster

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16 September 2017

language of work or name

English

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publication date

12 May 2009

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16 September 2017

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16 September 2017

volume

132

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16 September 2017

issue

Pt 6

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16 September 2017

page(s)

1613-1623

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Loss of PINK1 function affects development and results in neurodegeneration in zebrafish

16 September 2017

cites work

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Structure of the Parkin in-between-ring domain provides insights for E3-ligase dysfunction in autosomal recessive Parkinson's disease

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Parkin gene therapy could treat Parkinson's disease.

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'Rejuvenation' protects neurons in mouse models of Parkinson's disease

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

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Zebrafish as a new animal model for movement disorders

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Loss of PINK1 causes mitochondrial functional defects and increased sensitivity to oxidative stress

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Mitochondrial pathology and apoptotic muscle degeneration in Drosophila parkin mutants

21 January 2018

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Dopamine transporter expression distinguishes dopaminergic neurons from other catecholaminergic neurons in the developing zebrafish embryo.

21 January 2018

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Effect of wild-type or mutant Parkin on oxidative damage, nitric oxide, antioxidant defenses, and the proteasome

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A MicroRNA feedback circuit in midbrain dopamine neurons

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Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

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alpha -Synucleinopathy and selective dopaminergic neuron loss in a rat lentiviral-based model of Parkinson's disease.

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Analysis of alpha-synuclein, dopamine and parkin pathways in neuropathologically confirmed parkinsonian nigra

21 January 2018

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Mitochondrial function and morphology are impaired in parkin-mutant fibroblasts

21 January 2018

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Mitochondrial complex I and IV activities in leukocytes from patients with parkin mutations.

21 January 2018

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21 January 2018

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Structural comparison of zebrafish Elav/Hu and their differential expressions during neurogenesis.

21 January 2018

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Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin

21 January 2018

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Parkin-deficient mice are not a robust model of parkinsonism

21 January 2018

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The teleostean (zebrafish) dopaminergic system ascending to the subpallium (striatum) is located in the basal diencephalon (posterior tuberculum).

21 January 2018

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Connections of the ventral telencephalon and tyrosine hydroxylase distribution in the zebrafish brain (Danio rerio) lead to identification of an ascending dopaminergic system in a teleost

21 January 2018

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21 January 2018

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Mitochondria in the aetiology and pathogenesis of Parkinson's disease

21 January 2018

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Parkin localizes to the Lewy bodies of Parkinson disease and dementia with Lewy bodies

21 January 2018

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

21 January 2018

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Discovery and characterization of three novel synuclein genes in zebrafish

21 January 2018

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Calcium, ageing, and neuronal vulnerability in Parkinson's disease

21 January 2018

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High-resolution in situ hybridization to whole-mount zebrafish embryos

21 January 2018

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MPTP and DSP-4 susceptibility of substantia nigra and locus coeruleus catecholaminergic neurons in mice is independent of parkin activity

21 January 2018

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Visualization of monoaminergic neurons and neurotoxicity of MPTP in live transgenic zebrafish

21 January 2018

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Targeted mutagenesis in zebrafish

21 January 2018

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Mitochondrial pathology and muscle and dopaminergic neuron degeneration caused by inactivation of Drosophila Pink1 is rescued by Parkin

21 January 2018

1 reference

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

21 January 2018

1 reference

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Heterozygousparkinpoint mutations are as common in control subjects as in Parkinson's patients

21 January 2018

1 reference

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21 January 2018

Identifiers

DOI

10.1093/BRAIN/AWP108

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16 September 2017

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