(Q50509501)

English

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

scientific article published in May 1997

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9164619

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

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9164619

1 reference

based on heuristic

inferred from title

author name string

Fischel-Ghodsian N

1

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9164619

Prezant TR

2

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9164619

Chaltraw WE

3

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9164619

Wendt KA

4

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9164619

Nelson RA

5

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9164619

Arnos KS

6

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9164619

Falk RE

7

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9164619

publication date

1 May 1997

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9164619

American Journal of Otolaryngology

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9164619

18

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9164619

3

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9164619

173-178

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9164619

Genetic aspects of antibiotic induced deafness: mitochondrial inheritance

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2897%2990078-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2897%2990078-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2897%2990078-8

7 January 2021

based on heuristic

inferred from DOI database lookup

A molecular basis for human hypersensitivity to aminoglycoside antibiotics

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2897%2990078-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2897%2990078-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Hybridization of genomic DNA to oligonucleotide probes in the presence of tetramethylammonium chloride

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2897%2990078-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Sulfhydryl compounds and antioxidants inhibit cytotoxicity to outer hair cells of a gentamicin metabolite in vitro.

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2897%2990078-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0196-0709(97)90078-8

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9164619

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9164619

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