(Q24299953)

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Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia

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Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia (English)

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1 reference

based on heuristic

inferred from title

oxidative stress

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hereditary spastic paraplegia

1 reference

based on heuristic

inferred from title

Andrea Ballabio

5

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Laura Silvestri

2

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object named as

Laura Cassina

4

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object named as

Giorgio Casari

8

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author name string

Luigia Atorino

1

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Mirko Koppen

3

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Roberto Marconi

6

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Thomas Langer

7

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language of work or name

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publication date

24 November 2003

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Journal of Cell Biology

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163

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4

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777-87

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Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60

1 reference

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Identification and functional analysis of human Tom22 for protein import into mitochondria

1 reference

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Identification and characterization of AFG3L2, a novel paraplegin-related gene

1 reference

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Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease

1 reference

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A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3

1 reference

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The YTA10-12 complex, an AAA protease with chaperone-like activity in the inner membrane of mitochondria

1 reference

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Yta10p, a member of a novel ATPase family in yeast, is essential for mitochondrial function

1 reference

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Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics

1 reference

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Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia

1 reference

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AAA+ superfamily ATPases: common structure--diverse function

1 reference

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The human homologue of the yeast mitochondrial AAA metalloprotease Yme1p complements a yeast yme1 disruptant

1 reference

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1 reference

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Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

1 reference

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Protein misfolding, evolution and disease

1 reference

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1 reference

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1 reference

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2 references

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22 April 2017

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22 April 2017

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1 reference

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7 April 2017

Hereditary (familial) spastic paraplegia; further clinical and pathologic observations.

1 reference

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27 September 2017

Science in motion: common molecular pathological themes emerge in the hereditary spastic paraplegias

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1 reference

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1 reference

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SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia.

1 reference

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1 reference

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Molecular basis of inherited spastic paraplegias

1 reference

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Prion infection impairs the cellular response to oxidative stress

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AAA proteases: cellular machines for degrading membrane proteins

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1 reference

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https://api.crossref.org/works/10.1083%2FJCB.200304112

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Mitochondrial complex I deficiency in Parkinson's disease

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1083/JCB.200304112

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

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