Mitochondrial deafness mutations reviewed (Q33603767)

28 July 2017

1 reference

title

Mitochondrial deafness mutations reviewed (English)

1 reference

28 July 2017

main subject

mitochondrial deafness

1 reference

1 reference

Fischel-Ghodsian N

1

1 reference

28 July 2017

publication date

1 January 1999

1 reference

28 July 2017

1 reference

28 July 2017

volume

13

1 reference

28 July 2017

issue

4

1 reference

28 July 2017

page(s)

261-270

1 reference

Tissue-specific expression and chromosome assignment of genes specifying two isoforms of subunit VIIa of human cytochrome c oxidase

28 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

Biogenesis of mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

The Myoclonic Epilepsy and Ragged-Red Fiber Mutation Provides New Insights into Human Mitochondrial Function and Genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

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/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

Mitochondrial Genetics and Hearing Loss: The Missing Link between Genotype and Phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

Mitochondrial Mutations and Hearing Loss: Paradigm for Mitochondrial Genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

Mitochondrial mutation associated with nonsyndromic deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

Mitochondrial gene mutation is a significant predisposing factor in aminoglycoside ototoxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

Macular Pattern Retinal Dystrophy, Adult-onset Diabetes, and Deafness: A Family Study of A3243G Mitochondrial Heteroplasmy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

Genetic aspects of antibiotic induced deafness: mitochondrial inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

A molecular basis for human hypersensitivity to aminoglycoside antibiotics

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

Mutant mtDNA at 1555 A to G in 12S rRNA gene and hypersusceptibility of mitochondrial translation to streptomycin can be co-transferred to rho 0 HeLa cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

Sensorineural deafness inherited as a tissue specific mitochondrial disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNA(Leu(UUR)) gene mutation in Japanese patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

Presence of Mitochondrial large Ribosomal RNA Outside Mitochondria in Germ Plasm of Drosophila melanogaster

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

FAMILIAL SENSITIVITY TO STREPTOMYCIN.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

Mitochondrial DNA mutations and pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

Screening for mtDNA diabetes mutations in Pima Indians with NIDDM.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

Cochlear origin of hearing loss in MELAS syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNASer(UCN) gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

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/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

Phenotypic Expression of Diabetes Secondary to a T14709C Mutation of Mitochondrial DNA: Comparison with MIDD syndrome (A3243G mutation): a case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

Diseases of the mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

H-2M3 encodes the MHC Class I molecule presenting the maternally transmitted antigen of the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

10.1002/(SICI)1098-1004(1999)13:4<261::AID-HUMU1>3.0.CO;2-W

21 January 2018

Identifiers

DOI

1 reference

28 July 2017

1 reference