(Q44089250)

29 November 2017

title

Functional evaluation of paraplegin mutations by a yeast complementation assay (English)

1 reference

29 November 2017

Florian Bonn

1

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29 November 2017

Krishna Pantakani

2

1 reference

29 November 2017

Moneef Shoukier

3

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29 November 2017

Thomas Langer

4

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29 November 2017

Ashraf U Mannan

5

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29 November 2017

publication date

1 May 2010

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29 November 2017

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29 November 2017

volume

31

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29 November 2017

issue

5

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29 November 2017

page(s)

617-621

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Paraplegin gene analysis in hereditary spastic paraparesis (HSP) pedigrees in northeast England

29 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

The formation of respiratory chain complexes in mitochondria is under the proteolytic control of the m-AAA protease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

A clinical, genetic, and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

An intersubunit signaling network coordinates ATP hydrolysis by m-AAA proteases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

Paraplegin mutations in sporadic adult-onset upper motor neuron syndromes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

Hereditary spastic paraplegias: an update

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

Classification of the hereditary ataxias and paraplegias

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

Autocatalytic processing of m-AAA protease subunits in mitochondria

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

AAA proteases: cellular machines for degrading membrane proteins

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

Membrane protein degradation by AAA proteases in mitochondria: extraction of substrates from either membrane surface

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

SIFT: Predicting amino acid changes that affect protein function

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

Human non-synonymous SNPs: server and survey

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

Translating m-AAA protease function in mitochondria to hereditary spastic paraplegia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

AAA proteases in mitochondria: diverse functions of membrane-bound proteolytic machines

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

Hereditary spastic paraplegia caused by the novel mutation 1047insC in the SPG7 gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21226

7 January 2021

Identifiers

DOI

10.1002/HUMU.21226

1 reference

29 November 2017

1 reference