(Q48588748)

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Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons

scientific article published on 9 April 2006

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scholarly article

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Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/16604072

Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons (English)

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/16604072

mitochondrial DNA

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1 reference

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substantia nigra

1 reference

based on heuristic

inferred from title

3

object named as

Ann C McKee

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/16604072

author name string

Yevgenya Kraytsberg

1

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/16604072

Elena Kudryavtseva

2

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/16604072

Changiz Geula

4

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/16604072

Neil W Kowall

5

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/16604072

Konstantin Khrapko

6

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Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/16604072

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publication date

9 April 2006

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Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/16604072

Nature Genetics

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Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/16604072

38

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Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/16604072

5

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/16604072

518-520

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Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/16604072

The biologic clock: the mitochondria?

1 reference

https://api.crossref.org/works/10.1038%2FNG1778

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1778

7 January 2021

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The mitochondrial theory of aging: dead or alive?

1 reference

https://api.crossref.org/works/10.1038%2FNG1778

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1778

7 January 2021

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

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1778

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mtLOH (mitochondrial loss of heteroplasmy), aging, and 'surrogate self'.

1 reference

https://api.crossref.org/works/10.1038%2FNG1778

7 January 2021

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Single-molecule PCR: an artifact-free PCR approach for the analysis of somatic mutations

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Mitochondrial threshold effects.

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1778

7 January 2021

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Cell-by-cell scanning of whole mitochondrial genomes in aged human heart reveals a significant fraction of myocytes with clonally expanded deletions

1 reference

https://api.crossref.org/works/10.1038%2FNG1778

7 January 2021

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Prevalence of parkinsonian signs and associated mortality in a community population of older people

1 reference

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7 January 2021

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Parkinsonian signs and substantia nigra neuron density in decendents elders without PD

1 reference

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7 January 2021

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Mitochondrial DNA gene therapy: a gene therapy for aging?

1 reference

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Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/16604072

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

13 February 2018

http://europepmc.org/abstract/MED/16604072

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