Evidence map›Paper›PMID 11752454›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2001

Siah-1 binds and regulates the function of Numb.

L Susini, B J Passer, N Amzallag-Elbaz, T Juven-Gershon, S Prieur, N Privat, M Tuynder, M C Gendron, A Israël, R Amson and 2 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
–field-weighted citation impact
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

43 citing papers in PubMed.

  1. The CRL7Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Numb regulates the polarized delivery of cyclic nucleotide-gated ion channels in rod photoreceptor cilia.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  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

12 authors.

L SusiniMolecular Engines Laboratories, 20 Rue Bouvier, 75011 Paris, France.
B J Passer
N Amzallag-Elbaz
T Juven-Gershon
S Prieur
N Privat
M Tuynder
M C Gendron
A Israël
R Amson
M Oren
A Telerman

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Drosophila Seven in absentia (Sina) gene product originally was described as a protein that controls cell fate decisions during eye development. Its mammalian homolog, Siah-1, recently was found to be involved in p53-dependent and -independent pathways of apoptosis and G(1) arrest. We report that Siah-1 interacts directly with and promotes the degradation of the cell fate regulator Numb. Siah-1-mediated Numb degradation leads to redistribution of endogenous cell-surface Notch to the cytoplasm and nucleus and to augmented Notch-regulated transcriptional activity. These data imply that through its ability to target Numb for degradation, Siah-1 can act as a key regulator of Numb-related activities, including Notch signaling.

Indexed as

AnimalsApoptosisCell LineDown-RegulationDrosophilaDrosophila ProteinsHumansHydrolysisJuvenile HormonesMembrane ProteinsNuclear ProteinsOligonucleotides, AntisenseProtein BindingReceptors, NotchSeven in Absentia ProteinsTumor Suppressor Protein p53Drosophila ProteinsJuvenile HormonesMembrane ProteinsN protein, DrosophilaNuclear Proteinsnumb protein, DrosophilaOligonucleotides, AntisenseReceptors, NotchSeven in Absentia ProteinsTumor Suppressor Protein p53Ubiquitin-Protein Ligases

Identifiers

PMID11752454
PMCPMC64984

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.