Evidence map›Paper›PMID 9742153›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience1998

Genetic analysis on the role of integrin during axon guidance in Drosophila.

B Hoang, A Chiba

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
  2. Article
  3. Over-expression of Hsp83 in grossly depletedJournal of biosciences · 2019
    Article
  4. Review
  5. Review
  6. Src inhibits midline axon crossing independent of Frazzled/Deleted in Colorectal Carcinoma (DCC) receptor tyrosine phosphorylation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Genome-wide analyses of human perisylvian cerebral cortical patterning.Proceedings of the National Academy of Sciences of the United States of America · 2007
    Article
  14. Article
  15. Distinct roles of the beta 1-class integrins at the developing and the mature hippocampal excitatory synapse.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2006
    Article
  16. Article
  17. Integrins regulate responsiveness to slit repellent signals.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2002
    Article
  18. Article
  19. short stop is allelic to kakapo, and encodes rod-like cytoskeletal-associated proteins required for axon extension.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2000
    Article
  20. Dynamic visualization of nervous system in live Drosophila.Proceedings of the National Academy of Sciences of the United States of America · 1999
    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

2 authors at 1 institution in 1 country.

B HoangDepartment of Cell and Structural Biology, University of Illinois, Urbana, Illinois 61801, USA.
A Chiba
University of Illinois Urbana-Champaign · US

Funding

MOLECULAR MECHANISMS OF SYNAPTIC TARGET RECOGNITIONR01NS035049 · NINDS · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI CHIBA, AKIRA · 1996 to 2003
$1.2M
NINDS NIH HHS NS35049NINDS NIH HHS R01 NS035049
6 · The paper itself

Abstract

Heterodimeric cell surface receptor integrin is widely expressed in the nervous system, but its specific role during axon development has not been directly tested in vivo. We show that the Drosophila nervous system expresses low levels of positron-specific (PS) integrin subunits alphaPS1, alphaPS2, and betaPS during embryonic axogenesis. Furthermore, certain subsets of neurons express higher levels of integrin mRNAs than do the rest. Null mutations in either the alphaPS1 or alphaPS2 subunit gene cause widespread axon pathfinding errors that can be rescued by supplying the wild-type integrin subunit to the mutant nervous system. In contrast, misexpressing either the alphaPS1 or alphaPS2 integrin subunit in all neurons leads to no obvious axon pathfinding errors. We propose that integrin does not itself serve as either a "clutch" constituting molecule or a specific growth cone "receptor," as proposed previously, but rather as part of a molecular network that cooperatively guarantees accurate axon guidance.

Indexed as

AnimalsAntisense Elements (Genetics)AxonsDrosophilaGene Expression Regulation, DevelopmentalIntegrinsNeuronsRNA, MessengerAntisense Elements (Genetics)IntegrinsRNA, Messenger

Identifiers

PMID9742153
PMCPMC6793012
OpenAlexW2097861390

What OpenQuestion holds

Textmetadata
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.