Evidence map›Paper›PMID 29635765›Full record

ArticleAging cell2018

Mice with reduced expression of the telomere-associated protein Ft1 develop p53-sensitive progeroid traits.

Mattia La Torre, Chiara Merigliano, Romina Burla, Carla Mottini, Giorgia Zanetti, Simona Del Giudice, Mariateresa Carcuro, Ilaria Virdia, Elisabetta Bucciarelli, Isabella Manni and 9 more

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  5. p53 in the Molecular Circuitry of Bone Marrow Failure Syndromes.International journal of molecular sciences · 2023
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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

19 authors at 6 institutions in 2 countries.

Mattia La TorreDipartimento di Biologia e Biotecnologie "C. Darwin", Sapienza Università di Roma, Rome, Italy.
Chiara MeriglianoDipartimento di Biologia e Biotecnologie "C. Darwin", Sapienza Università di Roma, Rome, Italy.
Romina BurlaDipartimento di Biologia e Biotecnologie "C. Darwin", Sapienza Università di Roma, Rome, Italy.
Carla MottiniDipartimento di Biologia e Biotecnologie "C. Darwin", Sapienza Università di Roma, Rome, Italy.
Giorgia ZanettiDipartimento di Biologia e Biotecnologie "C. Darwin", Sapienza Università di Roma, Rome, Italy.
Simona Del GiudiceDipartimento di Biologia e Biotecnologie "C. Darwin", Sapienza Università di Roma, Rome, Italy.
Mariateresa CarcuroDipartimento di Biologia e Biotecnologie "C. Darwin", Sapienza Università di Roma, Rome, Italy.
Ilaria VirdiaDipartimento di Ricerca, Diagnostica Avanzata e Innovazione Tecnologica, Istituto Nazionale Tumori Regina Elena, Rome, Italy.
Elisabetta BucciarelliIstituto di Biologia e Patologia Molecolari del CNR, Rome, Italy.
Isabella ManniDipartimento di Ricerca, Diagnostica Avanzata e Innovazione Tecnologica, Istituto Nazionale Tumori Regina Elena, Rome, Italy.
Gianluca Rampioni VinciguerraAzienda Ospedaliera Sant'Andrea, Rome, Italy.
Giulia PiaggioDipartimento di Ricerca, Diagnostica Avanzata e Innovazione Tecnologica, Istituto Nazionale Tumori Regina Elena, Rome, Italy.
Mara RiminucciDipartimento di Medicina Molecolare, Sapienza Università di Roma, Rome, Italy.
Ana CumanoLymphopoiesis Unit, Institut Pasteur, Paris, France.
Armando BartolazziAzienda Ospedaliera Sant'Andrea, Rome, Italy.
Fiammetta VernìDipartimento di Biologia e Biotecnologie "C. Darwin", Sapienza Università di Roma, Rome, Italy.
Silvia SodduDipartimento di Ricerca, Diagnostica Avanzata e Innovazione Tecnologica, Istituto Nazionale Tumori Regina Elena, Rome, Italy.
Maurizio GattiDipartimento di Biologia e Biotecnologie "C. Darwin", Sapienza Università di Roma, Rome, Italy.
Isabella SaggioDipartimento di Biologia e Biotecnologie "C. Darwin", Sapienza Università di Roma, Rome, Italy.
Sapienza University of Rome · ITAzienda Ospedaliera Sant'Andrea · ITInstitute of Molecular Biology and Pathology · ITInstituto Nazionale Tumori Regina ElenaTecnologie Avanzate (Italy) · ITInstitut Pasteur · FR

Funding

Associazione Italiana per la Ricerca sul CancroEU FP7 Brainvectors 286071Fondazione TelethonProgeria Research Foundation
6 · The paper itself

Abstract

Human AKTIP and mouse Ft1 are orthologous ubiquitin E2 variant proteins involved in telomere maintenance and DNA replication. AKTIP also interacts with A- and B-type lamins. These features suggest that Ft1 may be implicated in aging regulatory pathways. Here, we show that cells derived from hypomorph Ft1 mutant (Ft1

Indexed as

AnimalsApoptosis Regulatory ProteinsCells, CulturedGene Expression ProfilingMiceMice, Inbred C57BLMutationProgeriaProteinsTumor Suppressor Protein p53Apoptosis Regulatory ProteinsFts protein, mouseProteinsTumor Suppressor Protein p53agingAKTIPDNA damagelaminsprogeriatelomeres

Identifiers

PMID29635765
PMCPMC6052474
OpenAlexW2798017833

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.