(Q45297269)

11 December 2017

title

Mitochondrial respiration and ATP production are significantly impaired in striatal cells expressing mutant huntingtin (English)

1 reference

11 December 2017

1 reference

Tamara Milakovic

1

1 reference

11 December 2017

Gail V W Johnson

series ordinal

2

1 reference

11 December 2017

language of work or name

English

0 references

publication date

27 June 2005

1 reference

Journal of Biological Chemistry

11 December 2017

number of pages

10

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

11 December 2017

volume

280

1 reference

11 December 2017

issue

35

1 reference

11 December 2017

page(s)

30773-30782

1 reference

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

11 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

Cerebral metabolism and atrophy in huntington's disease determined by18FDG and computed tomographic scan

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

Evidence for impairment of energy metabolism in vivo in Huntington's disease using localized 1H NMR spectroscopy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

Mitochondrial defect in Huntington's disease caudate nucleus

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

Oxidative damage and metabolic dysfunction in Huntington's disease: selective vulnerability of the basal ganglia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

Chronic mitochondrial energy impairment produces selective striatal degeneration and abnormal choreiform movements in primates

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

Pivotal role of oligomerization in expanded polyglutamine neurodegenerative disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

Specific progressive cAMP reduction implicates energy deficit in presymptomatic Huntington's disease knock-in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

Striatal cells from mutant huntingtin knock-in mice are selectively vulnerable to mitochondrial complex II inhibitor-induced cell death through a non-apoptotic pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

Early degenerative changes in transgenic mice expressing mutant huntingtin involve dendritic abnormalities but no impairment of mitochondrial energy production

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

Stabilization of mitochondrial functions with digitonin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

The measurement of the rotenone-sensitive NADH cytochrome c reductase activity in mitochondria isolated from minute amount of human skeletal muscle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

Characterization of the mitochondrial respiratory pathways in Candida albicans

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

In vivo control of respiration by cytochrome c oxidase in wild-type and mitochondrial DNA mutation-carrying human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

Sites of inhibition of mitochondrial electron transport in macrophage-injured neoplastic cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

The cytoskeleton of digitonin-treated rat hepatocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

Mitochondrial threshold effects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

Low reserve of cytochrome c oxidase capacity in vivo in the respiratory chain of a variety of human cell types.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

The energetics of Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

Metabolic and glutamatergic disturbances in the Huntington's disease transgenic mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

Partial resistance to malonate-induced striatal cell death in transgenic mouse models of Huntington's disease is dependent on age and CAG repeat length

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

Mice transgenic for the Huntington's disease mutation are resistant to chronic 3-nitropropionic acid-induced striatal toxicity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

Multiprotein complex containing succinate dehydrogenase confers mitochondrial ATP-sensitive K+ channel activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

Energy thresholds in brain mitochondria. Potential involvement in neurodegeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M504749200

21 January 2018

Identifiers

DOI

10.1074/JBC.M504749200

1 reference

11 December 2017

1 reference