(Q46157086)

20 December 2017

title

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

1 reference

20 December 2017

Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafness (English)

1 reference

21 August 2024

1 reference

1 reference

T. R. Prezant

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7689389

21 August 2024

J. V. Agapian

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7689389

21 August 2024

M. C. Bohlman

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7689389

21 August 2024

X. Bu

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7689389

21 August 2024

S. Oztas

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7689389

21 August 2024

W. Q. Qiu

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7689389

21 August 2024

K. S. Arnos

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7689389

21 August 2024

G. A. Cortopassi

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7689389

21 August 2024

L. Jaber

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7689389

21 August 2024

J. I. Rotter

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7689389

21 August 2024

language of work or name

English

0 references

publication date

1 July 1993

1 reference

20 December 2017

full work available at URL

http://www.nature.com/articles/ng0793-289

1 reference

http://www.nature.com/articles/ng0793-289.pdf

21 August 2024

file format

Portable Document Format

1 reference

21 August 2024

1 reference

20 December 2017

volume

1 reference

20 December 2017

issue

1 reference

20 December 2017

page(s)

289-294

1 reference

20 December 2017

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

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Genetic aspects of antibiotic induced deafness: mitochondrial inheritance

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Sensorineural deafness inherited as a tissue specific mitochondrial disorder

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Decoding at the ribosomal A site: antibiotics, misreading and energy of aminoacyl-tRNA binding.

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Interaction of antibiotics with functional sites in 16S ribosomal RNA

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Mapping of chloroplast mutations conferring resistance to antibiotics in Chlamydomonas: evidence for a novel site of streptomycin resistance in the small subunit rRNA.

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

A mutation in the 530 loop of Escherichia coli 16S ribosomal RNA causes resistance to streptomycin

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Two-locus mitochondrial and nuclear gene models for mitochondrial disorders

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Biochemical characterization of a pedigree with mitochondrially inherited deafness

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Sequence and organization of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Normal variants of human mitochondrial DNA and translation products: the building of a reference data base

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Detection of sickle cell beta S-globin allele by hybridization with synthetic oligonucleotides

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Analysis of enzymatically amplified β-globin and HLA-DQα DNA with allele-specific oligonucleotide probes

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Detecting single base substitutions as heteroduplex polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Trapped-oligonucleotide nucleotide incorporation (TONI) assay, a simple method for screening point mutations

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Compilation of small ribosomal subunit RNA sequences

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

A Compilation of large subunit RNA sequences presented in a structural format

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Sequence and gene organization of mouse mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

The complete nucleotide sequence of the Rattus norvegicus mitochondrial genome: cryptic signals revealed by comparative analysis between vertebrates

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Complete sequence of bovine mitochondrial DNA. Conserved features of the mammalian mitochondrial genome

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Polymorphism in mitochondrial DNA of humans as revealed by restriction endonuclease analysis

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Structure of ribosomal RNA

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

The emerging three-dimensional structure and function of 16S ribosomal RNA.

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy: evidence from segregation analysis for dependence on X chromosome inactivation

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-289

7 January 2021

Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy

1 reference

21 August 2024

Identifiers

DOI

10.1038/NG0793-289

1 reference

20 December 2017

1 reference

20 December 2017