Evidence map›Paper›PMID 18758477›Full record

ReviewOncogene2008

Notch3: from subtle structural differences to functional diversity.

D Bellavia, S Checquolo, A F Campese, M P Felli, A Gulino, I Screpanti

Open access · bronzeAbstract readReview
PubMed Publisher
In one paragraph

Review in Oncogene, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

51 citing papers in PubMed, 79 citations in OpenAlex.

  1. Trial
  2. Article
  3. Role of Notch signaling in corticalization.Journal of endocrinological investigation · 2026
    Review
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  5. Review
  6. Article
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  10. Review
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  15. Early diagnosis of lateral meningocele syndrome in an infant without neurological symptoms based on genomic analysis.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2022
    Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Review
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

6 authors at 1 institution in 1 country.

D BellaviaLaboratory of Molecular Pathology, Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
S Checquolo
A F Campese
M P Felli
A Gulino
I Screpanti
Sapienza University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Notch3 gene was identified, at the beginning of 90s, as the third mammalian Notch and was initially reported as being expressed in proliferating neuroepithelium. Since then, increasing evidence has demonstrated a number of structural and functional differences between Notch3 and both Notch1 and Notch2, which exhibit the highest structural similarity among the four mammalian Notch receptors. Possibly due to its more restricted tissue distribution, targeted deletion of murine Notch3 does not lead to embryonic lethality as is observed with targeted deletion of Notch1 and Notch2. However, genetic mutation, amplification and deregulated expression of Notch3 have been correlated with the disruption of cell differentiation in transgenic mice and to development of diseases in mice and humans. This review discusses the possible relationships between the structural differences and the nonredundant roles that Notch3 plays in the pathogenesis of the human disease cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy and in the regulation of murine T-cell differentiation and leukemogenesis.

Indexed as

AnimalsCADASILCell Transformation, NeoplasticDNA-Binding ProteinsGene Expression RegulationHumansImmunoglobulin J Recombination Signal Sequence-Binding ProteinLeukemia, ExperimentalMiceMice, TransgenicMutationOrgan SpecificityProtein BindingProtein Interaction Domains and MotifsReceptor, Notch3Receptors, NotchDNA-Binding ProteinsImmunoglobulin J Recombination Signal Sequence-Binding ProteinMAML1 protein, humanNOTCH3 protein, humanNotch3 protein, mouseReceptor, Notch3Receptors, NotchTrans-ActivatorsTranscription Factors

Identifiers

PMID18758477
OpenAlexW1964720708

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.