Evidence map›Paper›PMID 18797289›Full record

ReviewCurrent opinion in otolaryngology & head and neck surgery2008

The tectorial membrane: one slice of a complex cochlear sandwich.

Guy P Richardson, Andrei N Lukashkin, Ian J Russell

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in otolaryngology & head and neck surgery, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.2field-weighted citation impact, top 15% 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

42 citing papers in PubMed, 95 citations in OpenAlex.

  1. TECTB Variants Reveal Tectorial Membrane Vulnerability in Dominant Non-Syndromic Hearing Loss.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. Review
  3. ThemedRxiv : the preprint server for health sciences · 2025
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. PRDM16 expression and function in mammalian cochlear development.Developmental dynamics : an official publication of the American Association of Anatomists · 2022
    Article
  11. Review
  12. Article
  13. Article
  14. Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37.Genetics in medicine : official journal of the American College of Medical Genetics · 2019
    Article
  15. Article
  16. Old gene, new phenotype: splice-altering variants inJournal of medical genetics · 2018
    Article
  17. Article
  18. Review
  19. Neuroplastin Isoform Np55 Is Expressed in the Stereocilia of Outer Hair Cells and Required for Normal Outer Hair Cell Function.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    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

3 authors at 1 institution in 1 country.

Guy P RichardsonSchool of Life Sciences, University of Sussex, Falmer, Brighton, UK. g.p.richardson@sussex.ac.uk
Andrei N Lukashkin
Ian J Russell
University of Sussex · GB

Funding

Biotechnology and Biological Sciences Research CouncilMedical Research Council G0301057Medical Research Council G0801693Wellcome Trust 071394
6 · The paper itself

Abstract

purpose of reviewThe review is both timely and relevant, as recent findings have shown the tectorial membrane plays a more dynamic role in hearing than hitherto suspected, and that many forms of deafness can result from mutations in tectorial membrane proteins. RECENT

findingsMain themes covered are the molecular composition, the structural organization and properties of the tectorial membrane, the role of the tectorial membrane as a second resonator and a structure within which there is significant longitudinal coupling, and how mutations in tectorial membrane proteins cause deafness in mice and men.

conclusionFindings from experimental models imply that the tectorial membrane plays multiple, critical roles in hearing. These include coupling elements along the length of the cochlea, supporting a travelling wave and ensuring the gain and timing of cochlear feedback are optimal. The clinical findings suggest stable, moderate-to-severe forms of hereditary hearing loss may be diagnostic of a mutation in TECTA, a gene encoding one of the major, noncollagenous proteins of the tectorial membrane.

Indexed as

AnimalsCochleaDeafnessDisease Models, AnimalExtracellular Matrix ProteinsGene Expression RegulationGPI-Linked ProteinsHearingHearing Loss, SensorineuralMembrane GlycoproteinsMiceMice, TransgenicSensitivity and SpecificityTectorial MembraneExtracellular Matrix ProteinsGPI-Linked ProteinsMembrane GlycoproteinsTecta protein, mouse

Identifiers

PMID18797289
PMCPMC2874155
OpenAlexW2013755730

What OpenQuestion holds

Textmetadata
LicenceTDM
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.