Mitochondrial dysfunction in neurodegenerative disorders (Q40845642)

24 September 2017

title

Mitochondrial dysfunction in neurodegenerative disorders (English)

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24 September 2017

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A H Schapira

1

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24 September 2017

publication date

1 August 1998

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Biochimica et Biophysica Acta

24 September 2017

published in

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24 September 2017

volume

1366

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24 September 2017

issue

1-2

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24 September 2017

page(s)

225-233

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Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

24 September 2017

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AlaSOPro mutation in the gene encoding α-synuclein in Parkinson's disease

7 January 2021

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A large kindred with autosomal dominant Parkinson's disease

7 January 2021

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Mitochondrial complex I deficiency in Parkinson's disease

7 January 2021

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Evidence for mitochondrial dysfunction in Parkinson's disease--a critical appraisal

7 January 2021

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Alterations in glutathione levels in Parkinson's disease and other neurodegenerative disorders affecting basal ganglia

7 January 2021

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Anatomic and disease specificity of NADH CoQ1 reductase (complex I) deficiency in Parkinson's disease

7 January 2021

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Mitochondrial respiratory chain function in multiple system atrophy

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

A 31P magnetic resonance spectroscopy study of mitochondrial function in skeletal muscle of patients with Parkinson's disease

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Generalized mitochondrial dysfunction in Parkinson's disease detected by magnetic resonance spectroscopy of muscle

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Brain, skeletal muscle and platelet homogenate mitochondrial function in Parkinson's disease

7 January 2021

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Low platelet mitochondrial complex I and complex II/III activity in early untreated Parkinson's disease

7 January 2021

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Platelet mitochondrial function in Parkinson's disease. The Royal Kings and Queens Parkinson Disease Research Group

7 January 2021

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Origin and functional consequences of the complex I defect in Parkinson's disease

7 January 2021

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Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

7 January 2021

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MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts

7 January 2021

1 reference

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Complex I deficiency is associated with 3243G:C mitochondrial DNA in osteosarcoma cell cybrids

7 January 2021

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In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria

7 January 2021

1 reference

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Accumulation of mtDNA with a mutation at position 3271 in tRNA(Leu)(UUR) gene introduced from a MELAS patient to HeLa cells lacking mtDNA results in progressive inhibition of mitochondrial respiratory function

7 January 2021

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Mitochondrial control of nuclear apoptosis.

7 January 2021

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Induction of apoptotic program in cell-free extracts: requirement for dATP and cytochrome c

7 January 2021

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Sequential reduction of mitochondrial transmembrane potential and generation of reactive oxygen species in early programmed cell death

7 January 2021

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The mitochondrial generation of hydrogen peroxide. General properties and effect of hyperbaric oxygen

7 January 2021

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Increased apoptosis and early embryonic lethality in mice nullizygous for the Huntington's disease gene homologue

7 January 2021

1 reference

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A huntingtin-associated protein enriched in brain with implications for pathology

7 January 2021

1 reference

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HIP-I: a huntingtin interacting protein isolated by the yeast two-hybrid system

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Huntingtin is ubiquitinated and interacts with a specific ubiquitin-conjugating enzyme

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDH.

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Nuclear membrane indentations in Huntington's chorea

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Neuropathological changes of the nucleus accumbens in Huntington's chorea

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Mitochondrial function and parental sex effect in Huntington's disease

7 January 2021

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Mitochondrial defect in Huntington's disease caudate nucleus

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Requirement for superoxide in excitotoxic cell death

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Does impairment of energy metabolism result in excitotoxic neuronal death in neurodegenerative illnesses?

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Reversible inhibition of cytochrome c oxidase, the terminal enzyme of the mitochondrial respiratory chain, by nitric oxide. Implications for neurodegenerative diseases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Irreversible inhibition of mitochondrial complex I by 1-methyl-4-phenylpyridinium: evidence for free radical involvement

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Comparison of carbon monoxide, nitric oxide, and nitrite as inhibitors of the nitrogenase from Clostridium pasteurianum

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Nitrite Inhibition of Clostridium botulinum : Electron Spin Resonance Detection of Iron-Nitric Oxide Complexes

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Iron induced oxidative stress and mitochondrial dysfunction: relevance to Parkinson's disease

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Length of huntingtin and its polyglutamine tract influences localization and frequency of intracellular aggregates

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Friedreich's ataxia protein: phylogenetic evidence for mitochondrial dysfunction

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxin

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Frataxin gene of Friedreich's ataxia is targeted to mitochondria

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranes

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Respiratory deficiency due to loss of mitochondrial DNA in yeast lacking the frataxin homologue

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Temperature sensitive pet mutants in yeast Saccharomyces cerevisiae that lose mitochondrial RNA

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Heat shock protein HSP60 can alleviate the phenotype of mitochondrial RNA-deficient temperature-sensitive mna2 pet mutants

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Glucose metabolism alterations in Friedreich's ataxia

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Pyruvate oxidation in neuromuscular diseases. Evidence of a genetic defect in two families with the clinical syndrome of Friedreich's ataxia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Low Activities of the Pyruvate and Oxoglutarate Dehydrogenase Complexes in Five Patients with Friedreich's Ataxia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

The Quebec Cooperative Study of Friedreich's Ataxia: 1974-1984--10 years of research

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Aconitase and mitochondrial iron–sulphur protein deficiency in Friedreich ataxia

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Clinical and genetic abnormalities in patients with Friedreich's ataxia

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansion

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0005-2728%2898%2900115-7

10.1016/S0005-2728(98)00115-7

7 January 2021

Identifiers

DOI

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24 September 2017

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