Evidence map›Paper›PMID 19774094›Full record

ArticleExpert opinion on drug discovery2009

Using zebrafish to assess the impact of drugs on neural development and function.

Su Guo

Open access · greenAbstract read
In one paragraph

Article in Expert opinion on drug discovery, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

63 citing papers in PubMed, 159 citations in OpenAlex.

  1. Review
  2. Pharmaco-behavioral profiling identifies suppressors of autism gene-associated phenotypes in zebrafish.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Zebrafish as a high throughput model for organ preservation and transplantation research.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

3 more citing papers are in PubMed but not listed here.

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

1 author at 1 institution in 1 country.

Su GuoDepartment of Biopharmaceutical Sciences, Programs in Biological Sciences and Human Genetics, Institute for Regenerative Medicine, University of California San Francisco, CA 94143-2811.
California Institute for Regenerative Medicine · US

Funding

Development of Dopaminergic Neurons in ZebrafishR01NS042626 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GUO, SU · 2003 to 2012
$3.4M
An in vivo cellular model to study the biological effects of alcoholR01AA016021 · NIAAA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GUO, SU · 2006 to 2010
$1.8M
Chemical Genetics to Elucidate the Development of Dopaminergic NeuronsR01DA023904 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GUO, SU · 2008 to 2012
$1.7M
NIAAA NIH HHS R01 AA016021NIDA NIH HHS R01 DA023904NINDS NIH HHS R01 NS042626
6 · The paper itself

Abstract

backgroundZebrafish is becoming an increasingly attractive model organism for understanding biology and developing therapeutics, because as a vertebrate, it shares considerable similarity with mammals in both genetic compositions and tissue/organ structures, and yet remains accessible to high throughput phenotype-based genetic and small molecule compound screening. OBJECTIVE/

methodThe focus of this review is on the nervous system, which is arguably the most complex organ and known to be afflicted by more than six hundred disorders in humans. I discuss the past, present, and future of using zebrafish to assess the impact of small molecule drugs on neural development and function, in light of understanding and treating neurodevelopmental disorders such as autism, neurodegenerative disorders including Alzheimer's, Parkinson's, and Hungtington's disease, and neural system dysfunctions such as anxiety/depression and addiction.

conclusionThese studies hold promise to reveal fundamental mechanisms governing nervous system development and function, and to facilitate small molecule drug discovery for the many types of neurological disorders.

Identifiers

PMID19774094
PMCPMC2747263
OpenAlexW1989261569

What OpenQuestion holds

Textmetadata
LicenceTDM
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.