Evidence map›Paper›PMID 15014434›Full record

ArticleThe EMBO journal2004

Myo1c is designed for the adaptation response in the inner ear.

Christopher Batters, Christopher P Arthur, Abel Lin, Jessica Porter, Michael A Geeves, Ronald A Milligan, Justin E Molloy, Lynne M Coluccio

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

50 citing papers in PubMed, 86 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Actomyosin Complex.Sub-cellular biochemistry · 2022
    Article
  7. Functional Role of Class III Myosins in Hair Cells.Frontiers in cell and developmental biology · 2021
    Review
  8. Article
  9. Unconventional Myosins: How Regulation Meets Function.International journal of molecular sciences · 2019
    Review
  10. Article
  11. Article
  12. N-terminal splicing extensions of the humanThe Journal of biological chemistry · 2017
    Article
  13. Article
  14. Article
  15. Review
  16. Myosin-I molecular motors at a glance.Journal of cell science · 2016
    Review
  17. Article
  18. Beam finite-element model of a molecular motor for the simulation of active fibre networks.Proceedings. Mathematical, physical, and engineering sciences · 2016
    Article
  19. Mechanochemical tuning of myosin-I by the N-terminal region.Proceedings of the National Academy of Sciences of the United States of America · 2015
    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

8 authors at 3 institutions in 2 countries.

Christopher BattersDivision of Physical Biochemistry, National Institutes for Medical Research, The Ridgeway, Mill Hill, London, UK.
Christopher P Arthur
Abel Lin
Jessica Porter
Michael A Geeves
Ronald A Milligan
Justin E Molloy
Lynne M Coluccio
Scripps Research Institute · USBoston Biomedical Research Institute · USUniversity of Kent · GB

Funding

WORKSHOPS AND TRAININGP41RR017573 · NCRR · SCRIPPS RESEARCH INSTITUTE, THE · PI CARRAGHER, BRIDGET OLIVIA · 2002 to 2011
$14.2M
Molecular mechanism of a mammalian class I myosin motorR01GM068080 · NIGMS · BOSTON BIOMEDICAL RESEARCH INSTITUTE · PI COLUCCIO, LYNNE M · 2004 to 2007
$1.7M
AN INTEGRATED SYSTEM FOR MOLECULAR MICROSCOPYR01GM061939 · NIGMS · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI CARRAGHER, BRIDGET OLIVIA · 2000 to 2003
$1.6M
INSTRUMENTATION FOR SEPARATION &DETECTION OF MOLECULESS15GM039155 · NIGMS · UNIVERSITY OF KENTUCKY · PI SCHLOSS, JEFFREY A · 1987 to 1987
–
Medical Research Council MC_U117570592NCRR NIH HHS P41 RR017573NCRR NIH HHS RR17573NIGMS NIH HHS GM068080NIGMS NIH HHS GM39155NIGMS NIH HHS GM61939NIGMS NIH HHS R01 GM061939NIGMS NIH HHS R01 GM068080Wellcome Trust
6 · The paper itself

Abstract

The molecular motor, Myo1c, a member of the myosin family, is widely expressed in vertebrate tissues. Its presence at strategic places in the stereocilia of the hair cells in the inner ear and studies using transgenic mice expressing a mutant Myo1c that can be selectively inhibited implicate it as the mediator of slow adaptation of mechanoelectrical transduction, which is required for balance. Here, we have studied the structural, mechanical and biochemical properties of Myo1c to gain an insight into how this molecular motor works. Our results support a model in which Myo1c possesses a strain-sensing ADP-release mechanism, which allows it to adapt to mechanical load.

Indexed as

Adaptation, BiologicalAdenosine DiphosphateAnimalsCochleaCryoelectron MicroscopyHair Cells, AuditoryMechanotransduction, CellularMiceModels, MolecularMyosinsRatsStress, MechanicalAdenosine DiphosphateMyosins

Identifiers

PMID15014434
PMCPMC391074
OpenAlexW2133322584

What OpenQuestion holds

Textmetadata
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.