Evidence map›Paper›PMID 22343533›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2012

Wnt5a-Ror-Dishevelled signaling constitutes a core developmental pathway that controls tissue morphogenesis.

Hsin-Yi Henry Ho, Michael W Susman, Jay B Bikoff, Yun Kyoung Ryu, Andrea M Jonas, Linda Hu, Rejji Kuruvilla, Michael Eldon Greenberg

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 170 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
170citing papers in PubMed, 1 pooled it
10.3field-weighted citation impact, top 1% 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

170 citing papers in PubMed, 1 synthesis or guideline pooled it, 271 citations in OpenAlex.

  1. Pooled it
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  15. Ventral body wall closure: Mechanistic insights from mouse models and translation to human pathology.Developmental dynamics : an official publication of the American Association of Anatomists · 2025
    Review
  16. Review
  17. Unleashing Wnts: Wnt Ligands Fuel Cancer Spread.Journal of cancer biology · 2025
    Article
  18. Review
  19. Review
  20. Article

110 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Hsin-Yi Henry HoDepartment of Neurobiology, Harvard Medical School, Boston, MA 02115, USA.
Michael W Susman
Jay B Bikoff
Yun Kyoung Ryu
Andrea M Jonas
Linda Hu
Rejji Kuruvilla
Michael Eldon Greenberg
Harvard University · USJohns Hopkins University · US

Funding

Medical Scientist Training ProgramT32GM007753 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WALENSKY, LOREN DAVID · 1985 to 2021
$50.0M
SYNAPTIC MECHANISMS IN HIPPOCAMPAL EPILEPTOGENESISP30HD018655 · NICHD · CHILDREN'S HOSPITAL BOSTON · PI CHEN, CHINFEI · 1985 to 2015
$26.2M
Neurotrophic Factor Regulation of Gene ExpressionR01NS045500 · NINDS · HARVARD MEDICAL SCHOOL · PI GREENBERG, MICHAEL ELDON · 2003 to 2018
$8.2M
Neurotrophin mechanisms in neural development and diseaseR01NS073751 · NINDS · JOHNS HOPKINS UNIVERSITY · PI KURUVILLA, REJJI · 2011 to 2015
$1.7M
Crosstalk between neurotrophin and Wnt signaling pathways in neuronal developmentR01MH080738 · NIMH · JOHNS HOPKINS UNIVERSITY · PI KURUVILLA, REJJI · 2007 to 2011
$1.5M
NICHD NIH HHS P30 HD018655NICHD NIH HHS P30-HD 18655NIGMS NIH HHS T32 GM007753NIMH NIH HHS MH080738NIMH NIH HHS R01 MH080738NINDS NIH HHS R01 NS045500NINDS NIH HHS R01-NS-045500NINDS NIH HHS R01 NS073751PHS HHS T32 GMO7753-26
6 · The paper itself

Abstract

Wnts make up a large family of extracellular signaling molecules that play crucial roles in development and disease. A subset of noncanonical Wnts signal independently of the transcription factor β-catenin by a mechanism that regulates key morphogenetic movements during embryogenesis. The best characterized noncanonical Wnt, Wnt5a, has been suggested to signal via a variety of different receptors, including the Ror family of receptor tyrosine kinases, the Ryk receptor tyrosine kinase, and the Frizzled seven-transmembrane receptors. Whether one or several of these receptors mediates the effects of Wnt5a in vivo is not known. Through loss-of-function experiments in mice, we provide conclusive evidence that Ror receptors mediate Wnt5a-dependent processes in vivo and identify Dishevelled phosphorylation as a physiological target of Wnt5a-Ror signaling. The absence of Ror signaling leads to defects that mirror phenotypes observed in Wnt5a null mutant mice, including decreased branching of sympathetic neuron axons and major defects in aspects of embryonic development that are dependent upon morphogenetic movements, such as severe truncation of the caudal axis, the limbs, and facial structures. These findings suggest that Wnt5a-Ror-Dishevelled signaling constitutes a core noncanonical Wnt pathway that is conserved through evolution and is crucial during embryonic development.

Indexed as

Embryonic DevelopmentMorphogenesisWnt Signaling PathwayAdaptor Proteins, Signal TransducingAnimalsAxonsDishevelled ProteinsEmbryo, MammalianGene Expression Regulation, DevelopmentalMiceMice, Inbred C57BLMice, KnockoutPhosphoproteinsPhosphorylationProto-Oncogene Proteins c-junReceptor Tyrosine Kinase-like Orphan ReceptorsAdaptor Proteins, Signal TransducingDishevelled ProteinsPhosphoproteinsProto-Oncogene Proteins c-junReceptor Tyrosine Kinase-like Orphan ReceptorsRor1 protein, mouseRor2 protein, mouseWnt-5a ProteinWnt5a protein, mouseWnt Proteins

Identifiers

PMID22343533
PMCPMC3306699
OpenAlexW2141140780

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.