Evidence map›Paper›PMID 21818352›Full record

ArticlePloS one2011

Sh3pxd2b mice are a model for craniofacial dysmorphology and otitis media.

Bin Yang, Cong Tian, Zhi-guang Zhang, Feng-chan Han, Rami Azem, Heping Yu, Ye Zheng, Ge Jin, James E Arnold, Qing Y Zheng

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.8field-weighted citation impact, top 10% of its field
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

25 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. The A2ml1-Knockout mouse as an animal model for non-syndromic otitis media.International journal of pediatric otorhinolaryngology · 2024
    Article
  3. gom1 Mutant Mice as a Model of Otitis Media.Journal of the Association for Research in Otolaryngology : JARO · 2022
    Article
  4. Article
  5. Role of a novel mouse mutant of theFrontiers in neurology · 2022
    Article
  6. Hearing Loss in Id1Frontiers in genetics · 2021
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Panel 3: Genetics and Precision Medicine of Otitis Media.Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery · 2017
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

10 authors at 2 institutions in 2 countries.

Bin YangDepartment of Oral and Maxillofacial Surgery, Guanghua School of Stomatology, Sun Yat-Sen University, Guangzhou, China.
Cong Tian
Zhi-guang Zhang
Feng-chan Han
Rami Azem
Heping Yu
Ye Zheng
Ge Jin
James E Arnold
Qing Y Zheng
Case Western Reserve University · USSun Yat-sen University · CN

Funding

Deciphering the Usher I protein interactome using a genetic approachR01DC009246 · NIDCD · CASE WESTERN RESERVE UNIVERSITY · PI ZHENG, QING Y · 2009 to 2013
$1.6M
Transcriptome and Proteome Analysis of Mouse Inner EarsR01DC007392 · NIDCD · JACKSON LABORATORY · PI ZHENG, QING Y · 2005 to 2007
$1.0M
NIDCD NIH HHS R01 DC007392NIDCD NIH HHS R01DC007392NIDCD NIH HHS R01 DC009246NIDCD NIH HHS R01DC009246
6 · The paper itself

Abstract

Craniofacial defects that occur through gene mutation during development increase vulnerability to eustachian tube dysfunction. These defects can lead to an increased incidence of otitis media. We examined the effects of a mutation in the Sh3pxd2b gene (Sh3pxd2b(nee)) on the progression of otitis media and hearing impairment at various developmental stages. We found that all mice that had the Sh3pxd2b(nee) mutation went on to develop craniofacial dysmorphologies and subsequently otitis media, by as early as 11 days of age. We found noteworthy changes in cilia and goblet cells of the middle ear mucosa in Sh3pxd2b(nee) mutant mice using scanning electronic microscopy. By measuring craniofacial dimensions, we determined for the first time in an animal model that this mouse has altered eustachian tube morphology consistent with a more horizontal position of the eustachian tube. All mutants were found to have hearing impairment. Expression of TNF-α and TLR2, which correlates with inflammation in otitis media, was up-regulated in the ears of mutant mice when examined by immunohistochemistry and semi-quantitative RT-PCR. The mouse model with a mutation in the Sh3pxd2b gene (Sh3pxd2b(nee)) mirrors craniofacial dysmorphology and otitis media in humans.

Indexed as

AnimalsAuditory ThresholdCraniofacial AbnormalitiesDisease Models, AnimalEar, MiddleEvoked Potentials, Auditory, Brain StemGene Expression RegulationHearing LossHumansInflammationInflammation MediatorsMiceMice, Mutant StrainsMucous MembraneOtitis MediaPhenotypeFad49 protein, mouseInflammation MediatorsPhospholipid Transfer ProteinsTlr2 protein, mouseToll-Like Receptor 2Tumor Necrosis Factor-alpha

Identifiers

PMID21818352
PMCPMC3144925
OpenAlexW2048460968

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.