(Q34311330)

1 August 2017

Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body disease (English)

1 reference

1 August 2017

0 references

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7

Andrew J Lees

1 reference

1 August 2017

6

Thomas Arzberger

1 reference

1 August 2017

8

Rebecca A Betensky

1 reference

1 August 2017

9

M Flint Beal

1 reference

1 August 2017

Michael T Lin

1

1 reference

1 August 2017

Ippolita Cantuti-Castelvetri

2

1 reference

1 August 2017

Kangni Zheng

3

1 reference

1 August 2017

Katie E Jackson

4

1 reference

1 August 2017

Yong B Tan

5

1 reference

1 August 2017

David K Simon

10

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1 August 2017

1 June 2012

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1 August 2017

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1 August 2017

71

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1 August 2017

6

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1 August 2017

850-854

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Parkinson's disease brain mitochondria have impaired respirasome assembly, age-related increases in distribution of oxidative damage to mtDNA and no differences in heteroplasmic mtDNA mutation abundance

1 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383820

Incidental Lewy body disease and preclinical Parkinson disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383820

Mitochondria in the aetiology and pathogenesis of Parkinson's disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383820

High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383820

Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383820

Mitochondrial ND5 mutations in idiopathic Parkinson's disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383820

Stages in the development of Parkinson's disease-related pathology

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383820

Premature ageing in mice expressing defective mitochondrial DNA polymerase

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383820

Somatic mitochondrial DNA mutations in cortex and substantia nigra in aging and Parkinson's disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383820

High aggregate burden of somatic mtDNA point mutations in aging and Alzheimer's disease brain

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383820

Chronic systemic pesticide exposure reproduces features of Parkinson's disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383820

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383820

8-Hydroxyguanine, an abundant form of oxidative DNA damage, causes G-T and A-C substitutions

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383820

Evidence that incidental Lewy body disease is pre-symptomatic Parkinson's disease

6 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FANA.23568

Somatic mitochondrial DNA mutations in single neurons and glia.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FANA.23568

A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathy.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3383820

Deficiencies in complex I subunits of the respiratory chain in Parkinson's disease

28 October 2018

1 reference

12 December 2020

Familial multisystem degeneration with parkinsonism associated with the 11778 mitochondrial DNA mutation

1 reference

12 December 2020

Abnormalities of the electron transport chain in idiopathic Parkinson's disease

1 reference

12 December 2020

Mitochondrial complex I deficiency in Parkinson's disease

1 reference

12 December 2020

Identifiers

DOI

10.1002/ANA.23568

1 reference

1 August 2017

1 reference

1 August 2017

1 reference