(Q50477496)

English

[Prevalence of the A1555G mutation in the mitochondrial DNA in patients with cochlear or vestibular damage due to aminoglycoside-induced ototoxicity]

scientific article published in May 2004

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15461317%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

[Prevalence of the A1555G mutation in the mitochondrial DNA in patients with cochlear or vestibular damage due to aminoglycoside-induced ototoxicity] (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15461317%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

mitochondrial DNA

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based on heuristic

inferred from title

Carmelo Morales-Angulo

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15461317%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

author name string

J Gallo-Terán

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15461317%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

B Arellano

2

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15461317%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

S Modamio-Høybjør

4

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15461317%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

M A Moreno-Pelayo

5

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3 January 2020

R Ramírez-Camacho

6

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15461317%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

I del Castillo

7

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15461317%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

F Moreno

8

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Europe PubMed Central

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3 January 2020

publication date

1 May 2004

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3 January 2020

Acta Otorrinolaringológica Española

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15461317%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

55

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3 January 2020

5

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3 January 2020

212-217

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3 January 2020

Cross-linking of streptomycin to the 16S ribosomal RNA of Escherichia coli

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

Genetic factors in aminoglycoside toxicity

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

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%2FS0001-6519%2804%2978511-8

7 January 2021

Specific binding of aminoglycosides to a human rRNA construct based on a DNA polymorphism which causes aminoglycoside-induced deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

Genetic aspects of antibiotic induced deafness: mitochondrial inheritance

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

Prevalence of mitochondrial gene mutations among hearing impaired patients

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

Nonsyndromic hearing loss: an analysis of audiograms.

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

Predisposición familiar a la ototoxicidad de los aminoglucósidos debido a la mutación A1555G del ADN mitocondrial

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

[Audiometric features of familial hearing impairment transmitted by mitochondrial inheritance (A1555G)]

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

Genetic and clinical features of sensorineural hearing loss associated with the 1555 mitochondrial mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

Familial streptomycin ototoxicity in a South African family: a mitochondrial disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

Aminoglycoside-induced deafness associated with the mitochondrial DNA mutation A1555G.

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

Inherited susceptibility to aminoglycoside ototoxicity: genetic heterogeneity and clinical implications

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

Maternally inherited deafness associated with a T1095C mutation in the mDNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

Isepamicin sulfate-induced sensorineural hearing loss in patients with the 1555 A-->G mitochondrial mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

Modifier locus for mitochondrial DNA disease: linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12 S rRNA A1555G mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

Audiologic features of hearing loss due to the 1,555 mutation of mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

Mitochondrial deafness mutations reviewed

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

Audiovestibular findings in patients with deafness caused by a mitochondrial susceptibility mutation and precipitated by an inherited nuclear mutation or aminoglycosides.

1 reference

https://api.crossref.org/works/10.1016%2FS0001-6519%2804%2978511-8

7 January 2021

Identifiers

10.1016/S0001-6519(04)78511-8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15461317%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15461317%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

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