Evidence map›Paper›PMID 33618333›Full record

ArticleAging2021

Functional analysis of

Michela Murdocca, Paola Spitalieri, Claudia De Masi, Ion Udroiu, Jessica Marinaccio, Massimo Sanchez, Rosa Valentina Talarico, Chiara Fiorillo, Monica D'Adamo, Paolo Sbraccia and 4 more

Open access · greenAbstract read
In one paragraph

Article in Aging, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Case report: A novel splice-site mutation ofFrontiers in endocrinology · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Mutations Involved in Premature-Ageing Syndromes.The application of clinical genetics · 2021
    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

14 authors at 4 institutions in 1 country.

Michela MurdoccaDepartment of Biomedicine and Prevention, Tor Vergata University, Rome 00133, Italy.
Paola SpitalieriDepartment of Biomedicine and Prevention, Tor Vergata University, Rome 00133, Italy.
Claudia De MasiDepartment of Biomedicine and Prevention, Tor Vergata University, Rome 00133, Italy.
Ion UdroiuDepartment of Science, "Roma Tre" University, Rome 00154, Italy.
Jessica MarinaccioDepartment of Science, "Roma Tre" University, Rome 00154, Italy.
Massimo SanchezDepartment of Cell Biology and Neurosciences, Istituto Superiore di Sanità, Rome 00161, Italy.
Rosa Valentina TalaricoDepartment of Biomedicine and Prevention, Tor Vergata University, Rome 00133, Italy.
Chiara FiorilloPaediatric Neurology and Neuromuscular Disorders, University of Genoa and Istituto Gaslini, Genoa 16147, Italy.
Monica D'AdamoDepartment of Systems Medicine, Tor Vergata University, Rome 00133, Italy.
Paolo SbracciaDepartment of Systems Medicine, Tor Vergata University, Rome 00133, Italy.
Maria Rosaria D'ApiceLaboratory of Medical Genetics, Tor Vergata Hospital, Rome 00133, Italy.
Giuseppe NovelliDepartment of Biomedicine and Prevention, Tor Vergata University, Rome 00133, Italy.
Antonella SguraDepartment of Science, "Roma Tre" University, Rome 00154, Italy.
Federica SangiuoloDepartment of Biomedicine and Prevention, Tor Vergata University, Rome 00133, Italy.
University of Rome Tor Vergata · ITRoma Tre University · ITIstituto Superiore di Sanità · ITUniversity of Genoa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mandibular hypoplasia, Deafness and Progeroid features with concomitant Lipodystrophy define a rare systemic disorder, named MDPL Syndrome, due to almost always a

Indexed as

Acro-OsteolysisCellular SenescenceLipodystrophyPhenotypeSyndromeAdultDeafnessDNA Polymerase IIIDNA RepairFemaleHumansMandibleYoung AdultDNA Polymerase IIIPOLD1 protein, humanage-related diseaseDNA repairMDPL syndromePOLD1 genetelomere damage

Identifiers

PMID33618333
PMCPMC7950258
OpenAlexW3130876808

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.