(Q38473998)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9282897%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

title

Temporal bone analysis of patients with presbycusis reveals high frequency of mitochondrial mutations (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9282897%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9282897%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

author name string

N Fischel-Ghodsian

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9282897%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Y Bykhovskaya

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9282897%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

K Taylor

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9282897%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

T Kahen

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9282897%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

R Cantor

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9282897%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

K Ehrenman

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9282897%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

E Keithley

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9282897%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

language of work or name

1 reference

1 August 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9282897%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9282897%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

volume

110

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9282897%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

page(s)

147-154

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9282897%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

issue

1-2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9282897%20AND%20SRC:MED&resulttype=core&format=json

Biogenesis of mitochondria

5 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

17 A rapid alkaline extraction method for the isolation of plasmid DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

Ultrastructural features of neurons in the C57BL/6J mouse anteroventral cochlear nucleus: young mice versus old mice with chronic presbycusis

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

Deletion in Blood Mitochondrial DNA in Kearns-Sayre Syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

Mitochondrial mutation associated with nonsyndromic deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

Mitochondrial gene mutation is a significant predisposing factor in aminoglycoside ototoxicity.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

Correlations of differences in the density of innervation of the organ of Corti with differences in the acuity of hearing, including evidence as to the location in the human cochlea of the receptors for certain tones

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

Sensory and Neural Degeneration with Aging, as Seen in Microdissections of the Human Inner Ear

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

Strial atrophy in clinical and experimental deafness.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

Hair cell counts in an age-graded series of rat cochleas

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

Cochlear degeneration in aged rats of four strains

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

Bilateral sensorineural hearing loss associated with the point mutation in mitochondrial genome.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

Expression of mRNAs encoding alpha and beta subunit isoforms of the Na,K-ATPase in the rat cochlea.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

Cochlear pathology in presbycusis.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

Association of mitochondrial DNA deletions and cochlear pathology: a molecular biologic tool

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

Amplification of mitochondrial DNA from archival temporal bone specimens

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

Distinct genomic copy number in mitochondria of different mammalian organs.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

Liver mitochondrial respiratory functions decline with age

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

Occurrence of a particular base substitution (3243 A to G) in mitochondrial DNA of tissues of ageing humans

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2897%2900077-4

7 January 2021

10.1016/S0378-5955(97)00077-4

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9282897%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

1 reference