Evidence map›Paper›PMID 20362092›Full record

ArticleMethods in cell biology2009

The primary cilium as a Hedgehog signal transduction machine.

Sarah C Goetz, Polloneal J R Ocbina, Kathryn V Anderson

Open access · greenAbstract read
In one paragraph

Article in Methods in cell biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 108 papers.

0numbers the graph read from it
0cells of the map it votes in
108citing papers in PubMed
11.1field-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

108 citing papers in PubMed, 177 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Cells · 2025
    Review
  9. Regulation of INPP5E in Ciliogenesis, Development, and Disease.International journal of biological sciences · 2025
    Review
  10. Review
  11. Review
  12. Illumination of understudied ciliary kinases.Frontiers in molecular biosciences · 2024
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Zebrafish crocc2 mutants exhibit divergent craniofacial shape, misregulated variability, and aberrant cartilage morphogenesis.Developmental dynamics : an official publication of the American Association of Anatomists · 2023
    Article
  18. Review
  19. Appearing and disappearing acts of cilia.Journal of biosciences · 2023
    Review
  20. Astrocyte development-More questions than answers.Frontiers in cell and developmental biology · 2023
    Review

48 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

3 authors at 2 institutions in 1 country.

Sarah C GoetzDevelopmental Biology Program, Sloan-Kettering Institute, 1275 York Avenue, New York, New York 10065, USA.
Polloneal J R Ocbina
Kathryn V Anderson
Kettering University · USCornell University · US

Funding

Genetic Analysis of Mouse Nervous System DevelopmentR01NS044385 · NINDS · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI ANDERSON, KATHRYN V · 2002 to 2016
$7.0M
NINDS NIH HHS NS044385NINDS NIH HHS R01 NS044385
6 · The paper itself

Abstract

The Hedgehog (Hh) signal transduction pathway is essential for the development and patterning of numerous organ systems, and has important roles in a variety of human cancers. Genetic screens for mouse embryonic patterning mutants first showed a connection between mammalian Hh signaling and intraflagellar transport (IFT), a process required for construction of the primary cilium, a small cellular projection found on most vertebrate cells. Additional genetic and cell biological studies have provided very strong evidence that mammalian Hh signaling depends on the primary cilium. Here, we review the evidence that defines the integral roles that IFT proteins and cilia play in the regulation of the Hh signal transduction pathway in vertebrates. We discuss the mechanisms that control localization of Hh pathway proteins to the cilium, focusing on the transmembrane protein Smoothened (Smo), which moves into the cilium in response to Hh ligand. The phenotypes caused by loss of cilia-associated proteins are complex, which suggests that cilia and IFT play active roles in mediating Hh signaling rather than serving simply as a compartment in which pathway components are concentrated. Hh signaling in Drosophila does not depend on cilia, but there appear to be ancient links between cilia and components of the Hh pathway that may reveal how this fundamental difference between the Drosophila and mammalian Hh pathways arose in evolution.

Indexed as

AnimalsBody PatterningCiliaHedgehog ProteinsHumansMiceMutationReceptors, G-Protein-CoupledSignal TransductionHedgehog ProteinsReceptors, G-Protein-Coupled

Identifiers

PMID20362092
PMCPMC2867239
OpenAlexW1486014738

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.