Evidence map›Paper›PMID 33382037›Full record

ArticleeLife2020

Dysregulation of sonic hedgehog signaling causes hearing loss in ciliopathy mouse models.

Kyeong-Hye Moon, Ji-Hyun Ma, Hyehyun Min, Heiyeun Koo, HongKyung Kim, Hyuk Wan Ko, Jinwoong Bok

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

22 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. SHANK2 establishes auditory hair bundle architecture essential for mammalian hearing.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Article
  6. Tekt3 Safeguards Proper Functions and Morphology of Neuromast Hair Bundles.International journal of molecular sciences · 2025
    Article
  7. Article
  8. Article
  9. DNA Methylation Patterns Associated with Tinnitus in Young Adults-A Pilot Study.Journal of the Association for Research in Otolaryngology : JARO · 2024
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Follistatin regulates the specification of the apical cochlea responsible for low-frequency hearing in mammals.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  18. Article
  19. Article
  20. Animal models of developmental dyslexia.Frontiers in neuroscience · 2022
    Review
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

7 authors at 1 institution in 1 country.

Kyeong-Hye MoonDepartment of Anatomy, Yonsei University College of Medicine, Seoul, Republic of Korea.ORCID 0000-0002-6015-1690
Ji-Hyun MaDepartment of Anatomy, Yonsei University College of Medicine, Seoul, Republic of Korea.
Hyehyun MinDepartment of Anatomy, Yonsei University College of Medicine, Seoul, Republic of Korea.
Heiyeun KooDepartment of Anatomy, Yonsei University College of Medicine, Seoul, Republic of Korea.
HongKyung KimDepartment of Anatomy, Yonsei University College of Medicine, Seoul, Republic of Korea.
Hyuk Wan KoDepartment of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea.
Jinwoong BokDepartment of Anatomy, Yonsei University College of Medicine, Seoul, Republic of Korea.ORCID 0000-0003-1958-1872
Yonsei University · KR

Funding

National Research Foundation of Korea NRF-2014M3A9D5A01073865National Research Foundation of Korea NRF-2014M3A9D5A01073969National Research Foundation of Korea NRF-2016R1A5A2008630National Research Foundation of Korea NRF-2017R1A2B3009133
6 · The paper itself

Abstract

Defective primary cilia cause a range of diseases known as ciliopathies, including hearing loss. The etiology of hearing loss in ciliopathies, however, remains unclear. We analyzed cochleae from three ciliopathy mouse models exhibiting different ciliogenesis defects:

Indexed as

AnimalsCell PolarityCiliaCiliopathiesDisease Models, AnimalEmbryo, MammalianGene Expression Regulation, DevelopmentalHair Cells, AuditoryHearing LossHedgehog ProteinsMiceWnt Signaling PathwayHedgehog Proteinsciliopathiesdevelopmental biologyhearing lossmouseprimary ciliasonic hedgehog

Identifiers

PMID33382037
PMCPMC7806262
OpenAlexW3114771639

What OpenQuestion holds

Textmetadata
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.