Evidence map›Paper›PMID 32571922›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

The C terminus of p73 is essential for hippocampal development.

Ivano Amelio, Emanuele Panatta, Maria Victoria Niklison-Chirou, Joern R Steinert, Massimiliano Agostini, Nobuhiro Morone, Richard A Knight, Gerry Melino

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Deletion of p63 exon 13 in mice reveals C-terminal isoform-specific functions in epithelial development.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  3. Article
  4. Article
  5. Dichotomous transactivation domains contribute to growth inhibitory and promotion functions of TAp73.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  6. Article
  7. Article
  8. p73α1, a p73 C-terminal isoform, regulates tumor suppression and the inflammatory response via Notch1.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  9. Article
  10. Review
  11. Structural diversity of p63 and p73 isoforms.Cell death and differentiation · 2022
    Review
  12. Article
  13. Aging · 2021
    Article
  14. Review
  15. p73 as a Tissue Architect.Frontiers in cell and developmental biology · 2021
    Review
  16. Cancer predictive studies.Biology direct · 2020
    Review
  17. Regulation of Adult Neurogenesis in Mammalian Brain.International journal of molecular sciences · 2020
    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

8 authors at 3 institutions in 2 countries.

Ivano AmelioDepartment of Experimental Medicine, TOR Center, University of Rome Tor Vergata, 00133 Rome, Italy; ivano.amelio@uniroma2.it gm614@mrc-tox.cam.ac.uk.
Emanuele PanattaMedical Research Council, Toxicology Unit, University of Cambridge, Cambridge CB2 1QP, United Kingdom.ORCID 0000-0001-8723-9564
Maria Victoria Niklison-ChirouBlizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London E1 2AT, United Kingdom.ORCID 0000-0002-2147-370X
Joern R SteinertMedical Research Council, Toxicology Unit, University of Cambridge, Cambridge CB2 1QP, United Kingdom.ORCID 0000-0003-1640-0845
Massimiliano AgostiniDepartment of Experimental Medicine, TOR Center, University of Rome Tor Vergata, 00133 Rome, Italy.
Nobuhiro MoroneMedical Research Council, Toxicology Unit, University of Cambridge, Cambridge CB2 1QP, United Kingdom.
Richard A KnightMedical Research Council, Toxicology Unit, University of Cambridge, Cambridge CB2 1QP, United Kingdom.
Gerry MelinoDepartment of Experimental Medicine, TOR Center, University of Rome Tor Vergata, 00133 Rome, Italy; ivano.amelio@uniroma2.it gm614@mrc-tox.cam.ac.uk.ORCID 0000-0001-9428-5972
University of Cambridge · GBUniversity of Rome Tor Vergata · ITQueen Mary University of London · GB

Funding

Medical Research Council MC_U132681855
6 · The paper itself

Abstract

The p53 family member p73 has a complex gene structure, including alternative promoters and alternative splicing of the 3' UTR. This results in a complex range of isoforms whose biological relevance largely remains to be determined. By deleting exon 13 (which encodes a sterile α motif) from the Trp73 gene, we selectively engineered mice to replace the most abundantly expressed C-terminal isoform, p73α, with a shorter product of alternative splicing, p73β. These mice (

Indexed as

Alternative SplicingAnimalsApoptosisEmbryonic DevelopmentHippocampusHumansInterstitial Cells of CajalLearningMemoryMiceNeuronsPromoter Regions, GeneticTumor Protein p73Trp73 protein, mouseTumor Protein p73alternative splicingneurodevelopmentp53 family

Identifiers

PMID32571922
PMCPMC7355003
OpenAlexW3038006275

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.