Evidence map›Paper›PMID 26713509›Full record

ArticleThe Journal of comparative neurology2016

Molecular features distinguish ten neuronal types in the mouse superficial superior colliculus.

Haewon Byun, Soohyun Kwon, Hee-Jeong Ahn, Hong Liu, Douglas Forrest, Jonathan B Demb, In-Jung Kim

Abstract read
In one paragraph

Article in The Journal of comparative neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Recovery of Retinal Terminal Fields after Traumatic Brain Injury: Evidence of Collateral Sprouting and Sexual Dimorphism.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  2. Article
  3. Behavioral Modulation and Molecular Definition of Wide-Field Vertical Cells in the Mouse Superior Colliculus.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  4. Article
  5. Review
  6. Cadherin-13 Maintains Retinotectal Synapses via Transneuronal Interactions.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. A synaptic filtering mechanism in visual threat identification in mouse.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. A Novel Reporter Mouse Uncovers Endogenous Brn3b Expression.International journal of molecular sciences · 2019
    Article
  19. Divergent projection patterns of M1 ipRGC subtypes.The Journal of comparative neurology · 2018
    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

7 authors.

Haewon ByunDepartment of Ophthalmology and Visual Science, Yale University School of Medicine, New Haven, Connecticut, 06511.
Soohyun KwonDepartment of Ophthalmology and Visual Science, Yale University School of Medicine, New Haven, Connecticut, 06511.
Hee-Jeong AhnDepartment of Ophthalmology and Visual Science, Yale University School of Medicine, New Haven, Connecticut, 06511.
Hong LiuLaboratory of Endocrinology and Receptor Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, 20892.
Douglas ForrestLaboratory of Endocrinology and Receptor Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, 20892.
Jonathan B DembDepartment of Ophthalmology and Visual Science, Yale University School of Medicine, New Haven, Connecticut, 06511.
In-Jung KimDepartment of Ophthalmology and Visual Science, Yale University School of Medicine, New Haven, Connecticut, 06511.

Funding

Orphan nuclear receptors and mammalian developmentZIADK047035 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI FORREST, DOUGLAS · 2009 to 2025
$8.6M
Yale Core Grant for Vision ResearchP30EY026878 · NEI · YALE UNIVERSITY · PI In-Jung Kim · 2016 to 2026
$7.1M
Neural Circuits and Synapses for Early Visual ProcessingR01EY014454 · NEI · YALE UNIVERSITY · PI DEMB, JONATHAN B · 2005 to 2022
$6.7M
Molecular Specification of Direction Selectivity in the Visual SystemR00EY019355 · NEI · YALE UNIVERSITY · PI KIM, IN-JUNG · 2010 to 2012
$727k
NEI NIH HHS P30 EY026878NEI NIH HHS R00 EY019355NEI NIH HHS R01 EY014454
6 · The paper itself

Abstract

The superior colliculus (SC) is a midbrain center involved in controlling head and eye movements in response to inputs from multiple sensory modalities. Visual inputs arise from both the retina and visual cortex and converge onto the superficial layer of the SC (sSC). Neurons in the sSC send information to deeper layers of the SC and to thalamic nuclei that modulate visually guided behaviors. Presently, our understanding of sSC neurons is impeded by a lack of molecular markers that define specific cell types. To better understand the identity and organization of sSC neurons, we took a systematic approach to investigate gene expression within four molecular families: transcription factors, cell adhesion molecules, neuropeptides, and calcium binding proteins. Our analysis revealed 12 molecules with distinct expression patterns in mouse sSC: cadherin 7, contactin 3, netrin G2, cadherin 6, protocadherin 20, retinoid-related orphan receptor β, brain-specific homeobox/POU domain protein 3b, Ets variant gene 1, substance P, somatostatin, vasoactive intestinal polypeptide, and parvalbumin. Double labeling experiments, by either in situ hybridization or immunostaining, demonstrated that the 12 molecular markers collectively define 10 different sSC neuronal types. The characteristic positions of these cell types divide the sSC into four distinct layers. The 12 markers identified here will serve as valuable tools to examine molecular mechanisms that regulate development of sSC neuronal types. These markers could also be used to examine the connections between specific cell types that form retinocollicular, corticocollicular, or colliculothalamic pathways. J. Comp. Neurol. 524:2300-2321, 2016. © 2016 Wiley Periodicals, Inc.

Indexed as

AnimalsBiomarkersImage Processing, Computer-AssistedImmunohistochemistryIn Situ HybridizationMiceNeuronsSuperior ColliculiTranscriptomeBiomarkerscalcium binding proteinscell adhesion moleculesneuropeptidesretinal ganglion cellsRRID: AB_10000240RRID: AB_10000344RRID: AB_1288870RRID: AB_2079751RRID: AB_2167523RRID: AB_2298772RRID: AB_305869RRID: AB_518614RRID: AB_732196RRID: AB_91338RRID: nif-0000-00509RRID: nif-0000-30467transcription factors

Identifiers

PMID26713509
PMCPMC4892959

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Registered trials

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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.