(Q38422034)

2 September 2017

title

Quantification of the mitochondrial DNA common deletion in presbycusis (English)

1 reference

2 September 2017

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Adam Markaryan

1

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2 September 2017

Erik G Nelson

series ordinal

2

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2 September 2017

Raul Hinojosa

series ordinal

3

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2 September 2017

language of work or name

English

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publication date

1 June 2009

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2 September 2017

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2 September 2017

volume

119

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2 September 2017

issue

6

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2 September 2017

page(s)

1184-1189

1 reference

https://api.crossref.org/works/10.1002%2FLARY.20218

2 September 2017

1 reference

Presbycusis: A human temporal bone study of individuals with flat audiometric patterns of hearing loss using a new method to quantify stria vascularis volume

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.20218

Presbycusis: a human temporal bone study of individuals with downward sloping audiometric patterns of hearing loss and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.20218

Mitochondrial DNA deletion is a predisposing cause for sensorineural hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.20218

Technical report: laser microdissection of cochlear structures from celloidin embedded human temporal bone tissues and detection of the mitochondrial DNA common deletion using real time PCR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.20218

Mitochondrial threshold effects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.20218

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.20218

The ageing mitochondrial genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.20218

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.20218

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.20218

Temporal bone analysis of patients with presbycusis reveals high frequency of mitochondrial mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.20218

Mitochondrial dysfunction in hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.20218

The role of mitochondrial DNA large deletion for the development of presbycusis in Fischer 344 rats.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.20218

Premature ageing in mice expressing defective mitochondrial DNA polymerase

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.20218

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.20218

Correlation of Cochlear Blood Supply with Mitochondrial DNA Common Deletion in Presbyacusis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.20218

21 January 2018

Identifiers

DOI

10.1002/LARY.20218

1 reference

2 September 2017

1 reference