Evidence map›Paper›PMID 24477985›Full record

ArticleThe Journal of comparative neurology2014

DSCAM localization and function at the mouse cone synapse.

Gabriel Belem de Andrade, Samuel S Long, Harrison Fleming, Wei Li, Peter G Fuerst

Open access · greenAbstract readComparative Study
In one paragraph

Article in The Journal of comparative neurology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
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  7. DSCAM promotes self-avoidance in the developing mouse retina by masking the functions of cadherin superfamily members.Proceedings of the National Academy of Sciences of the United States of America · 2018
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  11. DSCAM-mediated control of dendritic and axonal arbor outgrowth enforces tiling and inhibits synaptic plasticity.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  12. DSCAM promotes axon fasciculation and growth in the developing optic pathway.Proceedings of the National Academy of Sciences of the United States of America · 2017
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  19. Design principles and developmental mechanisms underlying retinal mosaics.Biological reviews of the Cambridge Philosophical Society · 2015
    Review
  20. DSCAM promotes refinement in the mouse retina through cell death and restriction of exploring dendrites.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    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

5 authors at 5 institutions in 2 countries.

Gabriel Belem de AndradeDepartment of Biological Sciences, University of Idaho, Moscow, Idaho, 83844; Ministry of Education of Brazil, CAPES Foundation, Brasília-DF 70.040-020, Brazil.
Samuel S Long
Harrison Fleming
Wei Li
Peter G Fuerst
Brigham Young University - Idaho · USMinistry of Education · BRNational Eye Institute · USUniversity of Washington · USWashington State University · US

Funding

Women's health: interplay of maternal diet and key demographics on neurological health in the rural frontier and remote WestP20GM103408 · NIGMS · UNIVERSITY OF IDAHO · PI Scott A Minnich · 2012 to 2026
$59.8M
UNDERGRADUATE COLLEGE OUTREACH PROGRAMP20RR016454 · NCRR · UNIVERSITY OF IDAHO · PI CHASE, JENNIFER R · 2001 to 2011
$35.3M
Genomics Resources Core (GRC)P30GM103324 · NIGMS · UNIVERSITY OF IDAHO · PI FORNEY, LARRY J · 2013 to 2017
$5.0M
Role of molecular recognition in retinal patterning and synaptic organizationR01EY020857 · NEI · UNIVERSITY OF IDAHO · PI FUERST, PETER GERARD · 2010 to 2014
$1.2M
NCRR NIH HHS P20 RR016454NEI NIH HHS EY020857NEI NIH HHS R01 EY020857NIGMS NIH HHS P20 GM103408NIGMS NIH HHS P30 GM103324NIGMS NIH HHS P30 GM103324-01
6 · The paper itself

Abstract

The Down syndrome cell adhesion molecule (DSCAM) is required for regulation of cell number, soma spacing, and cell type-specific dendrite avoidance in many types of retinal ganglion and amacrine cells. In this study we assay the organization of cells making up the outer plexiform layer of the retina in the absence of Dscam. Some types of OFF bipolar cells, type 3b and type 4 bipolar cells, had defects in dendrite arborization in the Dscam mutant retina, whereas other cell types appeared similar to wild type. The cone synapses that these cells project their dendrites to were intact, as visualized by electron microscopy, and had a distribution and density that was not significantly different from that of wild type. The spacing of type 3b bipolar cell dendrites was further analyzed by Voronoi domain analysis, density recovery profiling (DRP) analysis, and nearest neighbor analysis. Spacing was found to be significantly different when wild-type and mutant type 3b bipolar cell dendrites were compared. Defects in arborization of these bipolar cells could not be attributed to the disorganization of inner plexiform layer cells that occurs in the Dscam mutant retina or an increase in cell number, as they arborized when Dscam was targeted in retinal ganglion cells only or in the bax null retina. Localization of DSCAM was assayed and the protein was localized near to cone synapses in mouse, macaque, and ground squirrel retinas. DSCAM protein was detected in several types of bipolar cells, including type 3b and type 4 bipolar cells.

Indexed as

Animalsbcl-2-Associated X ProteinCell Adhesion MoleculesCell CountDendritesFemaleMacacaMiceMice, Inbred C3HMice, Inbred C57BLMice, TransgenicMicroscopy, ElectronMutationRetinaRetinal Bipolar CellsRetinal Cone Photoreceptor CellsBax protein, mousebcl-2-Associated X ProteinCell Adhesion MoleculesDscam protein, mouseadhesionconeconnectomedevelopmentdifferential adhesion hypothesishorizontal cellmosaicpediclerodspherulesynapse

Identifiers

PMID24477985
PMCPMC4043867
OpenAlexW1937594456

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.