Cytochrome c oxidase defects of the human substantia nigra in normal aging (Q48865955)

16 February 2018

title

Cytochrome c oxidase defects of the human substantia nigra in normal aging (English)

1 reference

16 February 2018

1 reference

K. Itoh

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9363794

23 November 2024

S. Weis

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9363794

23 November 2024

P. Mehraein

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9363794

23 November 2024

J. Müller-Höcker

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9363794

23 November 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9363794

23 November 2024

publication date

1 November 1996

1 reference

16 February 2018

November 1996

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9363794

full work available at URL

23 November 2024

https://api.elsevier.com/content/article/PII:S0197458096001686?httpAccept=text/xml

1 reference

DOI

https://api.crossref.org/works/10.1016/S0197-4580(96)00168-6

https://api.elsevier.com/content/article/PII:S0197458096001686?httpAccept=text/plain

23 November 2024

1 reference

DOI

https://api.crossref.org/works/10.1016/S0197-4580(96)00168-6

23 November 2024

published in

Neurobiology of Aging

1 reference

16 February 2018

volume

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16 February 2018

issue

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16 February 2018

page(s)

843-848

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16 February 2018

Decline in skeletal muscle mitochondrial respiration chain function with ageing

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Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age

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Limited recovery of striatal dopaminergic fibers by adrenal medullary grafts in MPTP-treated aging mice

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MPTP-treated young mice but not aging mice show partial recovery of the nigrostriatal dopaminergic system by stereotaxic injection of acidic fibroblast growth factor (aFGF)

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Exogenous GM1 gangliosides induce partial recovery of the nigrostriatal dopaminergic system in MPTP-treated young mice but not in aging mice

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Ageing and Parkinson's disease: substantia nigra regional selectivity

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Chronic dietary pergolide preserves nigrostriatal neuronal integrity in aged-Fischer-344 rats

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Age-dependent increase in deleted mitochondrial DNA in the human heart: possible contributory factor to presbycardia

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Immunohistochemical studies on complexes I, II, III, and IV of mitochondria in Parkinson's disease

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Why are nigral catecholaminergic neurons more vulnerable than other cells in Parkinson's disease?

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Degeneration of the nigral dopamine neurons after 6-hydroxydopamine injection into the rat striatum

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Oxidative stress as a cause of nigral cell death in Parkinson's disease and incidental Lewy body disease. The Royal Kings and Queens Parkinson's Disease Research Group

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Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases

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Mitochondrial function and parental sex effect in Huntington's disease

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Aging and Extrapyramidal Function

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Oxidative damage to mitochondrial DNA shows marked age-dependent increases in human brain.

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Cytochrome c oxidase deficient fibres in the limb muscle and diaphragm of man without muscular disease: an age-related alteration

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7 January 2021

In situ hybridization of mitochondrial DNA in the heart of a patient with Kearns-Sayre syndrome and dilatative cardiomyopathy

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7 January 2021

Different in situ hybridization patterns of mitochondrial DNA in cytochrome c oxidase-deficient extraocular muscle fibres in the elderly

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Human aging is associated with various point mutations in tRNA genes of mitochondrial DNA.

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Reduced platelet cytochrome c oxidase activity in Alzheimer's disease.

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Electron transport chain defects in Alzheimer's disease brain

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Extensive loss of subcortical neurons in the aging rat brain

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

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7 January 2021

Mitochondrial DNA analysis in Parkinson's disease

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7 January 2021

Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial disease

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Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain

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Quantitative analysis of age-associated accumulation of mitochondrial DNA with deletion in human hearts

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DECLINE IN SKELETAL MUSCLE MITOCHONDRIAL RESPIRATORY CHAIN FUNCTION: POSSIBLE FACTOR IN AGEING

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Ageing-associated 5 kb deletion in human liver mitochondrial DNA.

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The anatomy and pigmentation of the human substantia nigra in relation to selective neuronal vulnerability

23 November 2024

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Monoaminergic neurotransmitter systems in presenile Alzheimer's disease and in senile dementia of Alzheimer type

23 November 2024

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

23 November 2024

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23 November 2024

Identifiers

DOI

1 reference

16 February 2018

1 reference

16 February 2018