Evidence map›Paper›PMID 31208058›Full record

ArticleCells2019

Modeling of

Disheet Shah, Laura Virtanen, Chandra Prajapati, Mostafa Kiamehr, Josef Gullmets, Gun West, Joose Kreutzer, Mari Pekkanen-Mattila, Tiina Heliö, Pasi Kallio and 2 more

Abstract read
In one paragraph

Article in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
–field-weighted citation impact
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

46 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. What Do We Know about Peripartum Cardiomyopathy? Yesterday, Today, Tomorrow.International journal of molecular sciences · 2024
    Review
  14. Cells · 2024
    Article
  15. Review
  16. Nuclear damage inMolecular biology of the cell · 2023
    Article
  17. Transcriptome studies of inherited dilated cardiomyopathies.Mammalian genome : official journal of the International Mammalian Genome Society · 2023
    Review
  18. Article
  19. Article
  20. 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

12 authors.

Disheet ShahBioMediTech, Faculty of Medicine and Health Technology; Tampere University, 33520 Tampere, Finland. Disheet.shah@tuni.fi.ORCID 0000-0002-8229-0835
Laura VirtanenInstitute of Biomedicine, University of Turku, 20520 Turku, Finland. latevi@utu.fi.ORCID 0000-0003-1921-1476
Chandra PrajapatiBioMediTech, Faculty of Medicine and Health Technology; Tampere University, 33520 Tampere, Finland. chandra.prajapati@tuni.fi.
Mostafa KiamehrBioMediTech, Faculty of Medicine and Health Technology; Tampere University, 33520 Tampere, Finland. mostafa.kiamehr@tuni.fi.ORCID 0000-0003-1894-3237
Josef GullmetsInstitute of Biomedicine, University of Turku, 20520 Turku, Finland. josef.gullmets@helsinki.fi.ORCID 0000-0003-2466-7574
Gun WestInstitute of Biomedicine, University of Turku, 20520 Turku, Finland. gun.west@utu.fi.
Joose KreutzerMicro-and Nanosystems Research Group, BioMediTech, Faculty of Medicine and Health Technology, Tampere University, 33140 Tampere, Finland. joose.kreutzer@tuni.fi.
Mari Pekkanen-MattilaBioMediTech, Faculty of Medicine and Health Technology; Tampere University, 33520 Tampere, Finland. Mari.Pekkanen-Mattila@tuni.fi.
Tiina HeliöHelsinki University Hospital, 00029 Helsinki, Finland. Tiina.Helio@hus.fi.ORCID 0000-0002-9640-9040
Pasi KallioMicro-and Nanosystems Research Group, BioMediTech, Faculty of Medicine and Health Technology, Tampere University, 33140 Tampere, Finland. pasi.kallio@tuni.fi.
Pekka TaimenInstitute of Biomedicine, University of Turku, 20520 Turku, Finland. pepeta@utu.fi.ORCID 0000-0001-8849-4604
Katriina Aalto-SetäläBioMediTech, Faculty of Medicine and Health Technology; Tampere University, 33520 Tampere, Finland. katriina.aalto-setala@tuni.fi.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dilated cardiomyopathy (DCM) is one of the leading causes of heart failure and heart transplantation. A portion of familial DCM is due to mutations in the

Indexed as

Models, BiologicalAdultAnimalsArrhythmias, CardiacCalciumCardiomyopathy, DilatedCell AggregationCell DifferentiationCell LineFemaleHumansHypoxiaInduced Pluripotent Stem CellsLamin Type AMaleMiceCalciumLamin Type Adilated cardiomyopathyhypoxiainduced pluripotent stem cellLamin A/CLMNAmicroelectrode array and calcium imaging

Identifiers

PMID31208058
PMCPMC6627421

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.