(Q37334174)

19 August 2017

1 reference

title

Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review (English)

1 reference

19 August 2017

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L Hema Bindu

1

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19 August 2017

P P Reddy

series ordinal

2

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19 August 2017

language of work or name

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1 November 2008

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International Journal of Audiology

19 August 2017

number of pages

6

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based on heuristic

inferred from page(s)

published in

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19 August 2017

volume

47

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19 August 2017

issue

11

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19 August 2017

page(s)

702-707

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Biogenesis of mitochondria

19 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Prevalence of the A1555G (12S rRNA) and tRNASer(UCN) mitochondrial mutations in hearing-impaired Brazilian patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Two large Spanish pedigrees with nonsyndromic sensorineural deafness and the mtDNA mutation at nt 1555 in the 12s rRNA gene: evidence of heteroplasmy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Audiologic testing and molecular analysis of 12S rRNA in patients receiving aminoglycosides

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

A molecular basis for human hypersensitivity to aminoglycoside antibiotics

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Mutations in the mitochondrial tRNA Ser(UCN) and in the GJB2 (connexin 26) gene are not modifiers of the age at onset or severity of hearing loss in Spanish patients with the 12S rRNA A1555G mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Molecular analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in paediatric subjects with non-syndromic hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Prevalence of the mitochondrial DNA A1555G mutation in sensorineural deafness patients in island Southeast Asia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Genetic epidemiology of hearing impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Genetics, genomics and gene discovery in the auditory system

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Ribosomal RNA and translation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

The A1555G mtDNA mutation in Danish hearing-impaired patients: frequency and clinical signs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Heterogenous point mutations in the mitochondrial tRNA Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from Mongolia

21 January 2018

1 reference

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

21 January 2018

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Genes responsible for human hereditary deafness: symphony of a thousand

21 January 2018

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Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Genetic susceptibility to aminoglycoside ototoxicity: how many are at risk?

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Prevalence of mitochondrial gene mutations among hearing impaired patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Maternally inherited non-syndromic hearing loss associated with mitochondrial 12S rRNA A827G mutation in a Chinese family.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Mitochondrial 12S rRNA A827G mutation is involved in the genetic susceptibility to aminoglycoside ototoxicity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Ototoxicity after use of neomycin eardrops is unrelated to A1555G point mutation in mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Human TRMU encoding the mitochondrial 5-methylaminomethyl-2-thiouridylate-methyltransferase is a putative nuclear modifier gene for the phenotypic expression of the deafness-associated 12S rRNA mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Aminoglycoside-induced hearing loss in a patient with the 961 mutation in mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Aminoglycoside-induced and non-syndromic hearing loss is associated with the G7444A mutation in the mitochondrial COI/tRNASer(UCN) genes in two Chinese families

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Screening of common mitochondrial mutations in Chinese patients with mitochondrial encephalomyopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802215862

10.1080/14992020802215862

21 January 2018

Identifiers

DOI

1 reference

19 August 2017

1 reference