Evidence map›Paper›PMID 10805794›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2000

Behavioral alterations associated with apoptosis and down-regulation of presenilin 1 in the brains of p53-deficient mice.

R Amson, J M Lassalle, H Halley, S Prieur, F Lethrosne, J P Roperch, D Israeli, M C Gendron, C Duyckaerts, F Checler and 4 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

26 citing papers in PubMed, 60 citations in OpenAlex.

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  10. Is Huntingtin Dispensable in the Adult Brain?Journal of Huntington's disease · 2017
    Review
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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

14 authors at 1 institution in 1 country.

R AmsonFondation Jean Dausset-Centre d'Etude du Polymorphisme Humain, 27 rue Juliette Dodu, 75010 Paris, France.
J M Lassalle
H Halley
S Prieur
F Lethrosne
J P Roperch
D Israeli
M C Gendron
C Duyckaerts
F Checler
J Dausset
D Cohen
M Oren
A Telerman
Université Toulouse III - Paul Sabatier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Presenilin 1 (PS1) expression is repressed by the p53 tumor suppressor. As shown herein, wild-type PS1 is an effective antiapoptotic molecule capable of significantly inhibiting p53-dependent and p53-independent cell death. We analyzed, at the functional and molecular levels, the brains of p53 knockout mice. Surprisingly, we found that lack of p53 expression induces apoptotic brain lesions, accompanied by learning deficiency and behavioral alterations. p53-deficient mice show an unexpected overexpression of p21(waf1) with subsequent down-regulation of PS1 in their brains. This process is progressive and age-dependent. These data indicate that the p53 pathway, besides affecting tumor suppression, may play a major role in regulating neurobehavioral function and cell survival in the brain.

Indexed as

Gene Expression RegulationAnimalsApoptosisBrainCloning, MolecularCyclin-Dependent Kinase Inhibitor p21CyclinsFemaleHumansIn Situ Nick-End LabelingMaleMaze LearningMembrane ProteinsMiceMice, Inbred C57BLMice, KnockoutCDKN1A protein, humanCdkn1a protein, mouseCyclin-Dependent Kinase Inhibitor p21CyclinsMembrane ProteinsPresenilin-1PSEN1 protein, humanTumor Suppressor Protein p53

Identifiers

PMID10805794
PMCPMC25831
OpenAlexW1993683227

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.