(Q29619113)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16604074%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

title

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

2 references

PubMed

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30 April 2017

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19 January 2020

1 reference

0 references

1 reference

1 reference

1

1 reference

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19 January 2020

Christopher Morris

3

1 reference

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Douglass Matthew Turnbull

19 January 2020

12

object named as

Douglass M Turnbull

1 reference

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19 January 2020

Robert William Taylor

11

object named as

Robert W Taylor

1 reference

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19 January 2020

10

Thomas Klopstock

1 reference

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19 January 2020

2

Kim J Krishnan

1 reference

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19 January 2020

7

Evelyn Jaros

1 reference

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19 January 2020

author name string

Geoffrey A Taylor

4

1 reference

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19 January 2020

Amy K Reeve

5

1 reference

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19 January 2020

Robert H Perry

6

1 reference

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19 January 2020

Joshua S Hersheson

8

1 reference

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19 January 2020

Joanne Betts

9

1 reference

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19 January 2020

language of work or name

1 reference

30 April 2017

publication date

9 April 2006

1 reference

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19 January 2020

2 references

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30 April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16604074%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

volume

38

2 references

PubMed

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30 April 2017

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19 January 2020

issue

5

2 references

PubMed

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30 April 2017

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19 January 2020

page(s)

515-517

1 reference

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Mitochondrial DNA mutations in human disease

19 January 2020

cites work

1 reference

Premature ageing in mice expressing defective mitochondrial DNA polymerase

1 May 2017

1 reference

A partial deficiency of cytochrome c oxidase in chronic progressive external ophthalmoplegia.

1 May 2017

1 reference

7 January 2021

Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy

1 reference

7 January 2021

Detection of a specific mitochondrial DNA deletion in tissues of older humans

1 reference

7 January 2021

Mitochondrial DNA mutations in human colonic crypt stem cells

1 reference

7 January 2021

Ageing and Parkinson's disease: substantia nigra regional selectivity

1 reference

7 January 2021

Gene expression profiling of rat midbrain dopamine neurons: implications for selective vulnerability in parkinsonism

1 reference

7 January 2021

The MPTP model of Parkinson's disease

1 reference

7 January 2021

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

1 reference

7 January 2021

Cytochrome c oxidase deficient cells accumulate in the hippocampus and choroid plexus with age.

1 reference

7 January 2021

Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCR.

1 reference

7 January 2021

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

1 reference

7 January 2021

Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.

1 reference

7 January 2021

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=16604074

Identifiers

3 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017

5351

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16604074%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

19 January 2020

1029731537

0 references

5351

1 reference

Consolidated OpenCitations Corpus – April 2017

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=16604074

3 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017

5351

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16604074%20AND%20SRC:MED&resulttype=core&format=json