Evidence map›Paper›PMID 37047537›Full record

ArticleInternational journal of molecular sciences2023

Altered Mitochondrial Dynamic in Lymphoblasts and Fibroblasts Mutated for

Nadia Bertola, Silvia Bruno, Cristina Capanni, Marta Columbaro, Andrea Nicola Mazzarello, Fabio Corsolini, Stefano Regis, Paolo Degan, Enrico Cappelli, Silvia Ravera

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  5. Article
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

10 authors at 4 institutions in 1 country.

Nadia BertolaDepartment of Experimental Medicine, University of Genoa, Via De Toni 14, 16132 Genova, Italy.ORCID 0000-0003-4591-3260
Silvia BrunoDepartment of Experimental Medicine, University of Genoa, Via De Toni 14, 16132 Genova, Italy.
Cristina CapanniCNR Institute of Molecular Genetics "Luigi Luca Cavalli-Sforza", Unit of Bologna, Via di Barbiano 1/10, 40136 Bologna, Italy.
Marta ColumbaroElectron Microscopy Platform, IRCCS Istituto Ortopedico Rizzoli, 40136 Bologna, Italy.
Andrea Nicola MazzarelloDepartment of Experimental Medicine, University of Genoa, Via De Toni 14, 16132 Genova, Italy.ORCID 0000-0003-2167-8817
Fabio CorsoliniLaboratory for the Study of Inborn Errors of Metabolism-Pediatric Clinic and Endocrinology IRCCS Istituto Giannina Gaslini, Via Gerolamo Gaslini 5, 16148 Genova, Italy.
Stefano RegisLaboratory of Clinical and Experimental Immunology, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy.ORCID 0000-0002-7723-2294
Paolo DeganU.O. Mutagenesis, IRCCS AOU San Martino-IST (Istituto Nazionale per la Ricerca sul Cancro), Largo Rosanna Benzi 10, 16132 Genova, Italy.
Enrico CappelliHematology Unit, IRCCS Istituto Giannina Gaslini, Via Gerolamo Gaslini 5, 16148 Genova, Italy.
Silvia RaveraDepartment of Experimental Medicine, University of Genoa, Via De Toni 14, 16132 Genova, Italy.ORCID 0000-0002-0803-1042
University of Genoa · ITIstituto Giannina Gaslini · ITIstituto Ortopedico Rizzoli · ITOspedale Policlinico San Martino · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fanconi anemia (FA) is a rare genetic disorder characterized by bone marrow failure and aplastic anemia. So far, 23 genes are involved in this pathology, and their mutations lead to a defect in DNA repair. In recent years, it has been observed that FA cells also display mitochondrial metabolism defects, causing an accumulation of intracellular lipids and oxidative damage. However, the molecular mechanisms involved in the metabolic alterations have not yet been elucidated. In this work, by using lymphoblasts and fibroblasts mutated for the

Indexed as

Fanconi AnemiaMitochondrial DynamicsDynaminsFanconi Anemia Complementation Group A ProteinFibroblastsHumansMitochondriaProteinsDynaminsFANCA protein, humanFanconi Anemia Complementation Group A ProteinProteinsaerobic metabolismFanconi anemiafissionfusionmitochondrial dynamicsOxPhos

Identifiers

PMID37047537
PMCPMC10094900
OpenAlexW4362470886

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.