A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

Sequence and gene organization of mouse mitochondrial DNA

1981 • 1,712 citations

Mitochondrial transcription factor A is necessary for mtDNA maintance and embryogenesis in mice

1998 • 1,517 citations

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

1993 • 1,173 citations

Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses

1999 • 815 citations

A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

1997 • 554 citations

A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase

1998 • 497 citations

Dilated cardiomyopathy and atrioventricular conduction blocks induced by heart-specific inactivation of mitochondrial DNA gene expression

1999 • 434 citations

Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes

2000 • 389 citations

Maternally transmitted histocompatibility antigen of mice: A hydrophobic peptide of a mitochondrially encoded protein

1990 • 324 citations

Quantitative measures of hair cell loss in CBA and C57BL/6 mice throughout their life spans

1997 • 268 citations

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

1996 • 236 citations

Mitochondrial deafness mutations reviewed

1999 • 222 citations

A Major Gene Affecting Age-Related Hearing Loss Is Common to at Least Ten Inbred Strains of Mice

2000 • 222 citations

Evidence from mtDNA sequences that common laboratory strains of inbred mice are descended from a single female

1982 • 202 citations

The Deafness-Associated Mitochondrial DNA Mutation at Position 7445, Which Affects tRNA^Ser(UCN) Precursor Processing, Has Long-Range Effects on NADH Dehydrogenase Subunit ND6 Gene Expression

1998 • 187 citations

Mitochondrial DNA deletions associated with aging and possibly presbycusis: a human archival temporal bone study.

1997 • 138 citations

Localization of the Usher syndrome type ID gene (Ush1D) to chromosome 10

1996 • 117 citations

The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse

1956 • 116 citations

Candidate Locus for a Nuclear Modifier Gene for Maternally Inherited Deafness

2000 • 113 citations

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

1997 • 105 citations

mdfw:A Deafness Susceptibility Locus That Interacts with Deaf Waddler (dfw)

1997 • 104 citations

Sensorineural deafness inherited as a tissue specific mitochondrial disorder.

1992 • 101 citations

Genetics of age-related hearing loss in mice. IV. Cochlear pathology and hearing loss in 25 BXD recombinant inbred mouse strains

1998 • 83 citations

Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22

1996 • 79 citations

Age-Related Degeneration of the Organ of Corti in Two Genotypes of Mice

1994 • 60 citations

Transfer of chloramphenicol-resistant mitochondrial DNA into the chimeric mouse.

1999 • 56 citations

A high-resolution genetic map around waltzer on mouse Chromosome 10 and identification of a new allele of waltzer

1997 • 26 citations

Mitochondrial RNA Processing and Translation: Link between Mitochondrial Mutations and Hearing Loss?

1998 • 21 citations

A single base substitution in the variable pocket of yeast tRNAArg eliminates species-specific aminoacylation

1999 • 16 citations