Pages that link to "Q50522021"

The following pages link to The deafness locus (dn) maps to mouse chromosome 19. (Q50522021):

Displaying 16 items.

• Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2 (Q28118979) (← links)
• Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function (Q28202014) (← links)
• Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses (Q29619783) (← links)
• TMC function in hair cell transduction (Q30413040) (← links)
• Genomic survey of prepulse inhibition in mouse chromosome substitution strains (Q30450693) (← links)
• Transmembrane channel-like (tmc) gene regulates Drosophila larval locomotion. (Q30780724) (← links)
• Beethoven, a mouse model for dominant, progressive hearing loss DFNA36. (Q34114643) (← links)
• Mouse models for human deafness: current tools for new fashions (Q34838323) (← links)
• Recessive mutations of TMC1 associated with moderate to severe hearing loss. (Q36698106) (← links)
• Genes responsible for human hereditary deafness: symphony of a thousand (Q41244075) (← links)
• Identification and mutation analysis of a cochlear-expressed, zinc finger protein gene at the DFNB7/11 and dn hearing-loss loci on human chromosome 9q and mouse chromosome 19. (Q48018820) (← links)
• Low intensities and 1.3 ratio produce distortion product otoacoustic emissions which are larger in heterozygous ( /dn) than homozygous ( / ) mice (Q50506026) (← links)
• The protective effect of metformin against the noise-induced hearing loss (Q57283655) (← links)
• The mouse deafness locus (dn) is associated with an inversion on chromosome 19 (Q57774687) (← links)
• Maturation of auditory brainstem projections and calyces in the congenitally deaf (dn/dn) mouse (Q80080013) (← links)
• Distinct functions of TMC channels: a comparative overview (Q90477574) (← links)