Evidence map›Paper›PMID 24707282›Full record

ArticleAudiology and neurotology. Extra2014

FVB/NJ mice demonstrate a youthful sensitivity to noise-induced hearing loss and provide a useful genetic model for the study of neural hearing loss.

Maria K Ho, Xin Li, Juemei Wang, Jeffrey D Ohmen, Rick A Friedman

Abstract read
In one paragraph

Article in Audiology and neurotology. Extra, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Current Advances in Adeno-Associated Virus-Mediated Gene Therapy to Prevent Acquired Hearing Loss.Journal of the Association for Research in Otolaryngology : JARO · 2022
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Osteoinductive potential of highly purified porous β-TCP in mice.Journal of materials science. Materials in medicine · 2015
    Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Maria K HoZilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, 90089 ; Department of Cell Biology and Genetics, House Research Institute, Los Angeles, CA 90057.
Xin LiDepartment of Cell Biology and Genetics, House Research Institute, Los Angeles, CA 90057.
Juemei WangZilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, 90089 ; Department of Cell Biology and Genetics, House Research Institute, Los Angeles, CA 90057.
Jeffrey D OhmenDepartment of Cell Biology and Genetics, House Research Institute, Los Angeles, CA 90057.
Rick A FriedmanZilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, 90089 ; Department of Cell Biology and Genetics, House Research Institute, Los Angeles, CA 90057.

Funding

Imaging CoreP30DC006276 · NIDCD · UNIVERSITY OF SOUTHERN CALIFORNIA · PI EISENBERG, LAURIE S · 2003 to 2016
$3.9M
High-Resolution Mapping of Susceptibility Genes for NIHLR01DC010856 · NIDCD · UNIVERSITY OF SOUTHERN CALIFORNIA · PI FRIEDMAN, RICK A · 2011 to 2015
$2.2M
NIDCD NIH HHS P30 DC006276NIDCD NIH HHS R01 DC010856
6 · The paper itself

Abstract

The hybrid mouse diversity panel (HMDP), a panel of 100 strains, has been employed in genome wide association studies (GWAS) to study complex traits in mice. Hearing is a complex trait and the CBA/CaJ mouse strain is a widely used model for age-related hearing loss (ARHI) and noise induced hearing loss (NIHL). The CBA/CaJ strain's youthful sensitivity to noise and limited age-related loss led us to attempt to identify additional strains segregating a similar phenotype for our panel. FVB/NJ is part of the HMDP and has been previously described as having a similar ARHI phenotype to CBA/CaJ. For these reasons, we have studied the FVB/NJ mouse for ARHI and NIHL phenotypes in hopes of incorporating its phenotype into HMDP studies. We demonstrate that FVB/NJ exhibits ARHI at an earlier age than CBA/CaJ and young FVB/NJ mice are vulnerable to NIHL up until 10 to 12 weeks. This suggests that FVB/NJ may be used as an additional genetic model for neural forms of progressive hearing loss and for the study of youthful sensitivity to noise.

Indexed as

age-related hearing impairmentauditory brainstem responsedistortion product otoacoustic emissionsFVB/NJ miceHybrid mouse diversity panelnoise-induced hearing loss

Identifiers

PMID24707282
PMCPMC3972069

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.