Insights into mitochondrial quality control pathways and Parkinson's disease. (Q38104226)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23644494%20AND%20SRC:MED&resulttype=core&format=json

29 February 2020

title

Insights into mitochondrial quality control pathways and Parkinson's disease (English)

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29 February 2020

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1

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29 February 2020

author name string

L Miguel Martins

series ordinal

2

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29 February 2020

language of work or name

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4 May 2013

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Journal of Molecular Medicine

29 February 2020

published in

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29 February 2020

volume

91

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29 February 2020

issue

6

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29 February 2020

page(s)

665-671

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https://scigraph.springernature.com/pub.10.1007/s00109-013-1044-y

29 February 2020

exact match

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cites work

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The bioenergetic and antioxidant status of neurons is controlled by continuous degradation of a key glycolytic enzyme by APC/C-Cdh1.

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In situ localization of mitochondrial DNA replication in intact mammalian cells

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Spatial parkin translocation and degradation of damaged mitochondria via mitophagy in live cortical neurons

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ClpP mediates activation of a mitochondrial unfolded protein response in C. elegans

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Ubiquitin-like protein 5 positively regulates chaperone gene expression in the mitochondrial unfolded protein response

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The matrix peptide exporter HAF-1 signals a mitochondrial UPR by activating the transcription factor ZC376.7 in C. elegans

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PINK1 protects against oxidative stress by phosphorylating mitochondrial chaperone TRAP1

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Mitochondrial quality control and Parkinson's disease: a pathway unfolds

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Fission and selective fusion govern mitochondrial segregation and elimination by autophagy

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Developmentally regulated mitochondrial fusion mediated by a conserved, novel, predicted GTPase.

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OPA1 requires mitofusin 1 to promote mitochondrial fusion

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Drosophila parkin requires PINK1 for mitochondrial translocation and ubiquitinates mitofusin

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PINK1 and Parkin target Miro for phosphorylation and degradation to arrest mitochondrial motility

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

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PARIS (ZNF746) repression of PGC-1α contributes to neurodegeneration in Parkinson's disease

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Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23644494%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

29 February 2020

0 references

1 reference

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