2012
DOI: 10.3766/jaaa.23.5.4
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Inheritance Patterns of Noise Vulnerability and “Protectability” in (C57BL/6J × CBA/J) F1 Hybrid Mice

Abstract: Our data support the hypothesis that young CBA/J and B6 mice carry different alleles that underlie their divergent responses to KM and sensitivities to noise exposure. While the number and type of genes remain unknown, they are worth pursuing because they establish completely novel hearing phenotypes with potential relevance to humans. Our results lay the foundation for mapping of the underlying genes, and ultimately gene identification.

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Cited by 6 publications
(3 citation statements)
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“…This comprehensive study design with both positive (noise) and negative (water) controls confirms the findings of many previous studies regarding the severity and consistency of noise-related damage to auditory function (Johnson 1993, Barden et al 2012). For combination treatment, a similar strategy to studies on the interactions of styrene and noise was used (Mäkitie et al 2003; Venet et al 2015).…”
Section: Discussionsupporting
confidence: 86%
“…This comprehensive study design with both positive (noise) and negative (water) controls confirms the findings of many previous studies regarding the severity and consistency of noise-related damage to auditory function (Johnson 1993, Barden et al 2012). For combination treatment, a similar strategy to studies on the interactions of styrene and noise was used (Mäkitie et al 2003; Venet et al 2015).…”
Section: Discussionsupporting
confidence: 86%
“…We used CBA mice which are commonly used in studies of noise-induced hearing loss [54]. Although they have been shown to have increased noise susceptibility compared to C57Bl/6J mice at younger ages, they do not have the age-related hearing loss associated with this strain [55], [56]. As well, other strains of mice have been shown to have even more alterations in noise susceptibility [57].…”
Section: Discussionmentioning
confidence: 99%
“…These types of strains have greatly assisted in identifi cation of novel genetic variants associated with ARHL (Nemoto et al 2004 ;Johnson et al 2012 ). Similar approaches should prove useful to characterize the genetic basis of known strain differences in auditory function, including differences in responses to noise stress , protection from conditioning stresses (Barden et al 2012 ), and aging (Noben-Trauth and Johnson 2009 ;NobenTrauth et al 2010 ;Schacht et al 2012 ).…”
Section: Mouse Modelsmentioning
confidence: 99%