Evidence map›Paper›PMID 31519693›Full record

ReviewDisease models & mechanisms2019

Modeling hematopoietic disorders in zebrafish.

Martina Konantz, Christoph Schürch, Pauline Hanns, Joëlle S Müller, Loïc Sauteur, Claudia Lengerke

Open access · goldAbstract readReview
In one paragraph

Review 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
1.8field-weighted citation impact, top 17% 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, 33 citations in OpenAlex.

  1. Review
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  8. Zebrafish: A Tractable Model for Analysis of T Cell Development.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  9. Haematopoiesis in Zebrafish (Danio Rerio).Frontiers in immunology · 2022
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
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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

6 authors at 1 institution in 1 country.

Martina KonantzDepartment of Biomedicine, University of Basel and University Hospital Basel, Basel 4031, Switzerland martina.konantz@unibas.ch.ORCID 0000-0002-4319-3119
Christoph SchürchDepartment of Biomedicine, University of Basel and University Hospital Basel, Basel 4031, Switzerland.
Pauline HannsDepartment of Biomedicine, University of Basel and University Hospital Basel, Basel 4031, Switzerland.
Joëlle S MüllerDepartment of Biomedicine, University of Basel and University Hospital Basel, Basel 4031, Switzerland.
Loïc SauteurDepartment of Biomedicine, University of Basel and University Hospital Basel, Basel 4031, Switzerland.
Claudia LengerkeDepartment of Biomedicine, University of Basel and University Hospital Basel, Basel 4031, Switzerland.ORCID 0000-0001-5442-2805
University of Basel · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Zebrafish offer a powerful vertebrate model for studies of development and disease. The major advantages of this model include the possibilities of conducting reverse and forward genetic screens and of observing cellular processes by

Indexed as

Disease Models, AnimalHematopoiesisAnimalsDrug Evaluation, PreclinicalHematologic DiseasesZebrafishBlood disordersBone marrow failure syndromeDisease modelsHematopoiesisImmunodeficiencyLeukemia

Identifiers

PMID31519693
PMCPMC6765189
OpenAlexW2971360522

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.