Evidence map›Paper›PMID 28332227›Full record

ReviewThe Journal of physiology2017

General features of inhibition in the inner retina.

Katrin Franke, Tom Baden

Open access · bronzeAbstract readReview
In one paragraph

Review in The Journal of physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

28 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Altered Functional Responses of the Retina in B6 Albino Tyrc/c Mice.Investigative ophthalmology & visual science · 2024
    Article
  8. Review
  9. Review
  10. On the Functional Role of Gamma Synchronization in the Retinogeniculate System of the Cat.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  11. Article
  12. Functional properties of GABAFrontiers in ophthalmology · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Retina regeneration: lessons from vertebrates.Oxford open neuroscience · 2022
    Review
  18. Article
  19. A retinal circuit for the suppressed-by-contrast receptive field of a polyaxonal amacrine cell.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  20. Observational
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 2 institutions in 2 countries.

Katrin FrankeCentre for Integrative Neuroscience, University of Tübingen, Germany.
Tom BadenInstitute for Ophthalmic Research, Tübingen, Germany.
Bernstein Center for Computational Neuroscience Tübingen · DEUniversity of Sussex · GB

Funding

Vertically integrated approach to visual neuroscience: microcircuits to behaviorU01NS090562 · NINDS · PRINCETON UNIVERSITY · PI EULER, THOMAS, HUBERMAN, ANDREW D · 2014 to 2016
$3.6M
Retinal circuits for local synaptic processingR01EY023766 · NEI · UNIVERSITY OF PENNSYLVANIA · PI EULER, THOMAS, SMITH, ROBERT G · 2014 to 2017
$1.0M
NEI NIH HHS R01 EY023766NINDS NIH HHS U01 NS090562
6 · The paper itself

Abstract

Visual processing starts in the retina. Within only two synaptic layers, a large number of parallel information channels emerge, each encoding a highly processed feature like edges or the direction of motion. Much of this functional diversity arises in the inner plexiform layer, where inhibitory amacrine cells modulate the excitatory signal of bipolar and ganglion cells. Studies investigating individual amacrine cell circuits like the starburst or A17 circuit have demonstrated that single types can possess specific morphological and functional adaptations to convey a particular function in one or a small number of inner retinal circuits. However, the interconnected and often stereotypical network formed by different types of amacrine cells across the inner plexiform layer prompts that they should be also involved in more general computations. In line with this notion, different recent studies systematically analysing inner retinal signalling at a population level provide evidence that general functions of the ensemble of amacrine cells across types are critical for establishing universal principles of retinal computation like parallel processing or motion anticipation. Combining recent advances in the development of indicators for imaging inhibition with large-scale morphological and genetic classifications will help to further our understanding of how single amacrine cell circuits act together to help decompose the visual scene into parallel information channels. In this review, we aim to summarise the current state-of-the-art in our understanding of how general features of amacrine cell inhibition lead to general features of computation.

Indexed as

Amacrine CellsAnimalsPattern Recognition, Visualamacrine cellcomputationGABAglycineinhibitionneuronal networkretinavision

Identifiers

PMID28332227
PMCPMC5556161
OpenAlexW2598846857

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.