Evidence map›Paper›PMID 30833296›Full record

ArticleDisease models & mechanisms2019

The zebrafish orthologue of the human hepatocerebral disease gene

Laura Martorano, Margherita Peron, Claudio Laquatra, Elisa Lidron, Nicola Facchinello, Giacomo Meneghetti, Natascia Tiso, Andrea Rasola, Daniele Ghezzi, Francesco Argenton

Open access · goldAbstract read
In one paragraph

Article in Disease models & mechanisms, 2019. 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
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

17 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Genes · 2021
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Opa1 Overexpression Protects from Early-Onset Mpv17Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Article
  14. Article
  15. Genome and Transcriptome Sequencing ofInternational journal of molecular sciences · 2020
    Article
  16. Article
  17. 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 2 institutions in 1 country.

Laura MartoranoDepartment of Biology, University of Padova, Via Ugo Bassi, 58/B, 35131 Padova, Italy.
Margherita PeronDepartment of Biology, University of Padova, Via Ugo Bassi, 58/B, 35131 Padova, Italy.
Claudio LaquatraDepartment of Biomedical Sciences, University of Padova, Via Ugo Bassi, 58/B, 35131 Padova, Italy.
Elisa LidronDepartment of Biomedical Sciences, University of Padova, Via Ugo Bassi, 58/B, 35131 Padova, Italy.
Nicola FacchinelloDepartment of Biology, University of Padova, Via Ugo Bassi, 58/B, 35131 Padova, Italy.
Giacomo MeneghettiDepartment of Biology, University of Padova, Via Ugo Bassi, 58/B, 35131 Padova, Italy.
Natascia TisoDepartment of Biology, University of Padova, Via Ugo Bassi, 58/B, 35131 Padova, Italy.
Andrea RasolaDepartment of Biomedical Sciences, University of Padova, Via Ugo Bassi, 58/B, 35131 Padova, Italy.
Daniele GhezziUnit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Amadeo 42, 20133 Milan, Italy.
Francesco ArgentonDepartment of Biology, University of Padova, Via Ugo Bassi, 58/B, 35131 Padova, Italy francesco.argenton@unipd.it.ORCID 0000-0002-0803-8236
University of Padua · ITUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondrial DNA depletion syndromes (MDS) are a group of rare autosomal recessive disorders with early onset and no cure available. MDS are caused by mutations in nuclear genes involved in mitochondrial DNA (mtDNA) maintenance, and characterized by both a strong reduction in mtDNA content and severe mitochondrial defects in affected tissues. Mutations in

Indexed as

Genetic PleiotropySequence Homology, Amino AcidAnimalsBiosynthetic PathwaysDNA, MitochondrialElectron TransportGene DosageHumansLarvaLiverMembrane ProteinsMitochondriaMitochondrial DiseasesMitochondrial ProteinsMutationNucleotidesDNA, MitochondrialMembrane ProteinsMitochondrial ProteinsMPV17 protein, humanMpv17 protein, zebrafishNucleotidespyrimidinePyrimidinesZebrafish ProteinsDihydroorotate dehydrogenaseIridophoreMitochondrial DNA depletion syndromePyrimidineVitamin B13

Identifiers

PMID30833296
PMCPMC6451431
OpenAlexW2918751188

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.