C57BL/6 (B6) mice experience hearing loss and cochlear degeneration beginning about mid-life, whereas CAST/Ei (CAST) mice retain normal hearing until old age. A locus contributing to the hearing loss of B6 mice, named age-related hearing loss (ahl), was mapped to Chromosome 10. A homozygous, congenic strain of mice (B6.CAST-+ahl ), generated by crossing B6 (ahl/ahl) and CAST (+ahl/+ahl) mice has the same genomic material as the B6 mice except in the region of the ahl locus, which is derived from CAST. In this study, we have determined the extent of the CAST-derived region of Chromosome 10 in the congenic strain and have examined mice of all three strains for hearing loss and cochlear morphology between 9 and 25 months of age. Resul...
Genetic modifiers can be detected in mice by looking for strain background differences in inheritanc...
The human ortholog of the gene responsible for audiogenic seizure susceptibility in Frings and BUB/B...
Both the ahl allele of Cdh23 and the null mutation of Sod1 have been shown to contribute to age-rela...
A major gene responsible for age-related hearing loss (AHL) in C57BL/6J mice was mapped by analyses ...
Inbred strains of mice offer promising models for understanding the genetic basis of human presbycus...
Inbred mouse strains with age-related hearing loss (AHL) provide valuable models for studying the ge...
The ahl locus, shown to be a strain-specific Cdh23 dimorphism, contributes to age-related hearing lo...
AbstractThe DBA/2J inbred strain of mice is used extensively in hearing research, yet little is know...
The DBA/2J inbred strain of mice is used extensively in hearing research, yet little is known about ...
Inbred strain variants of the Cdh23 gene have been shown to influence the onset and progression of a...
Positional cloning of mouse deafness mutations uncovered a plethora of proteins that have important ...
The effects of genotype and diet on age-related hearing loss were evaluated using auditory brainstem...
Progressive sensorineural hearing loss is the most common form of acquired hearing impairment in the...
Inbred mouse strains serve as important models for human presbycusis or age-related hearing loss. We...
Noise-induced hearing loss (NIHL) is one of the more common sources of environmentally induced heari...
Genetic modifiers can be detected in mice by looking for strain background differences in inheritanc...
The human ortholog of the gene responsible for audiogenic seizure susceptibility in Frings and BUB/B...
Both the ahl allele of Cdh23 and the null mutation of Sod1 have been shown to contribute to age-rela...
A major gene responsible for age-related hearing loss (AHL) in C57BL/6J mice was mapped by analyses ...
Inbred strains of mice offer promising models for understanding the genetic basis of human presbycus...
Inbred mouse strains with age-related hearing loss (AHL) provide valuable models for studying the ge...
The ahl locus, shown to be a strain-specific Cdh23 dimorphism, contributes to age-related hearing lo...
AbstractThe DBA/2J inbred strain of mice is used extensively in hearing research, yet little is know...
The DBA/2J inbred strain of mice is used extensively in hearing research, yet little is known about ...
Inbred strain variants of the Cdh23 gene have been shown to influence the onset and progression of a...
Positional cloning of mouse deafness mutations uncovered a plethora of proteins that have important ...
The effects of genotype and diet on age-related hearing loss were evaluated using auditory brainstem...
Progressive sensorineural hearing loss is the most common form of acquired hearing impairment in the...
Inbred mouse strains serve as important models for human presbycusis or age-related hearing loss. We...
Noise-induced hearing loss (NIHL) is one of the more common sources of environmentally induced heari...
Genetic modifiers can be detected in mice by looking for strain background differences in inheritanc...
The human ortholog of the gene responsible for audiogenic seizure susceptibility in Frings and BUB/B...
Both the ahl allele of Cdh23 and the null mutation of Sod1 have been shown to contribute to age-rela...