Evidence map›Paper›PMID 20452772›Full record

ReviewTrends in cell biology2010

Yorkie: the final destination of Hippo signaling.

Hyangyee Oh, Kenneth D Irvine

Open access · greenAbstract readReview
In one paragraph

Review in Trends in cell biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

98 citing papers in PubMed, 170 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Hippo signaling regulates cuticle pigmentation and dopamine metabolism inbioRxiv : the preprint server for biology · 2025
    Article
  7. RNAi-based screen for pigmentation inbioRxiv : the preprint server for biology · 2025
    Article
  8. Review
  9. Hippo effector, Yorkie, is a tumor suppressor in selectProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Juvenile hormone-induced histone deacetylase 3 suppresses apoptosis to maintain larval midgut in the yellow fever mosquito.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  17. Review
  18. Near-infrared nuclear markers formicroPublication biology · 2022
    Article
  19. Tumor-Induced Cardiac Dysfunction: A Potential Role of ROS.Antioxidants (Basel, Switzerland) · 2021
    Article
  20. Role of FAT1 in health and disease.Oncology letters · 2021
    Review

38 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

2 authors at 2 institutions in 1 country.

Hyangyee OhHoward Hughes Medical Institute, Waksman Institute and Department of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ 08854, USA.
Kenneth D Irvine
Howard Hughes Medical Institute · USRutgers, The State University of New Jersey · US

Funding

Growth regulation by the Fat signaling pathwayR01GM078620 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI IRVINE, KENNETH D · 2007 to 2018
$3.3M
Transcriptional regulation of growth downstream of tumor suppressor pathwaysF32GM079817 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI OH, HYANGYEE · 2007 to 2009
$144k
Howard Hughes Medical InstituteNIGMS NIH HHS 1F32GM079817NIGMS NIH HHS F32 GM079817NIGMS NIH HHS GM078620NIGMS NIH HHS R01 GM078620
6 · The paper itself

Abstract

The Hippo signaling pathway is a key regulator of growth during animal development, whereas loss of normal Hippo pathway activity is associated with a wide range of cancers. Hippo signaling represses growth by inhibiting the activity of a transcriptional co-activator protein, known as Yorkie in Drosophila and Yap in vertebrates. In the 5 years since the first report linking Yorkie to Hippo signaling, intense interest in this pathway has led to rapid increases in our understanding of the action and regulation of Yorkie/Yap, which we review here. These studies have also emphasized the complexity of Yorkie/Yap regulation, including multiple, distinct mechanisms for repressing its transcriptional activity, and multiple DNA-binding partner proteins that can direct Yorkie to distinct downstream target genes.

Indexed as

Signal TransductionAnimalsDrosophila ProteinsHippo KinasesHumansIntracellular Signaling Peptides and ProteinsNuclear ProteinsProtein Serine-Threonine KinasesTrans-ActivatorsYAP-Signaling ProteinsDrosophila ProteinsHippo Kinaseshpo protein, DrosophilaIntracellular Signaling Peptides and ProteinsNuclear ProteinsProtein Serine-Threonine KinasesTrans-ActivatorsYAP-Signaling ProteinsYki protein, Drosophila

Identifiers

PMID20452772
PMCPMC2919348
OpenAlexW2029985957

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.