Evidence map›Paper›PMID 19712673›Full record

ArticleDevelopmental biology2009

Myosin-X is critical for migratory ability of Xenopus cranial neural crest cells.

Shuyi Nie, Yun Kee, Marianne Bronner-Fraser

Abstract read
In one paragraph

Article in Developmental biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

24 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Myosin X Interaction with KIF13B, a Crucial Pathway for Netrin-1-Induced Axonal Development.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  3. Review
  4. Article
  5. MMP14 Regulates Cranial Neural Crest Epithelial-to-Mesenchymal Transition and Migration.Developmental dynamics : an official publication of the American Association of Anatomists · 2018
    Article
  6. Article
  7. Genetic Requirement ofPlastic and reconstructive surgery. Global open · 2018
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Myosin-10 produces its power-stroke in two phases and moves processively along a single actin filament under low load.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  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

3 authors at 2 institutions in 1 country.

Shuyi NieDivision of Biology 139-74, California Institute of Technology, Pasadena, CA 91125, USA.
Yun Kee
Marianne Bronner-Fraser
California Institute of Technology · USNational Institutes of Health · US

Funding

Transcriptional Casualty in Embryonic Morphogenesis: from the Specifications GRNP01HD037105 · NICHD · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI DAVIDSON, ERIC H · 1999 to 2018
$27.1M
Induction of the Neural CrestR37NS036585 · NINDS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI BRONNER, MARIANNE · 2002 to 2008
$2.9M
INDUCTION OF THE NEURAL CRESTR01NS036585 · NINDS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI BRONNER-FRASER, MARIANNE · 1998 to 2001
$553k
NICHD NIH HHS HD037105NICHD NIH HHS P01 HD037105NINDS NIH HHS NS36585NINDS NIH HHS R01 NS036585NINDS NIH HHS R37 NS036585
6 · The paper itself

Abstract

The neural crest is a highly migratory cell population, unique to vertebrates, that forms much of the craniofacial skeleton and peripheral nervous system. In exploring the cell biological basis underlying this behavior, we have identified an unconventional myosin, myosin-X (Myo10) that is required for neural crest migration. Myo10 is highly expressed in both premigratory and migrating cranial neural crest (CNC) cells in Xenopus embryos. Disrupting Myo10 expression using antisense morpholino oligonucleotides leads to impaired neural crest migration and subsequent cartilage formation, but only a slight delay in induction. In vivo grafting experiments reveal that Myo10-depleted CNC cells migrate a shorter distance and fail to segregate into distinct migratory streams. Finally, in vitro cultures and cell dissociation-reaggregation assays suggest that Myo10 may be critical for cell protrusion and cell-cell adhesion. These results demonstrate an essential role for Myo10 in normal cranial neural crest migration and suggest a link to cell-cell interactions and formation of processes.

Indexed as

SkullXenopus laevisAnimalsCarrier ProteinsCell AdhesionCell MovementCell Surface ExtensionsEmbryonic InductionGene Knockdown TechniquesMyosinsNeural CrestNoggin ProteinOligonucleotides, AntisenseTransplantsTwist-Related Protein 1Xenopus ProteinsCarrier ProteinsMyo10 protein, XenopusMyosinsNoggin ProteinOligonucleotides, AntisenseTwist-Related Protein 1Xenopus Proteins

Identifiers

PMID19712673
PMCPMC3991693
OpenAlexW2160364334

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.