Evidence map›Paper›PMID 26727264›Full record

ArticlePloS one2016

Geniculo-Cortical Projection Diversity Revealed within the Mouse Visual Thalamus.

Marcus N Leiwe, Aenea C Hendry, Andrew D Bard, Stephen J Eglen, Andrew S Lowe, Ian D Thompson

Abstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

6 authors.

Marcus N LeiweMRC Centre for Developmental Neurobiology, King's College London, Guy's Campus, London, United Kingdom.
Aenea C HendryMRC Centre for Developmental Neurobiology, King's College London, Guy's Campus, London, United Kingdom.
Andrew D BardMRC Centre for Developmental Neurobiology, King's College London, Guy's Campus, London, United Kingdom.
Stephen J EglenCambridge Computational Biology Institute, Department of Applied Mathematics and Theoretical Physics, University of Cambridge, Cambridge, United Kingdom.
Andrew S LoweMRC Centre for Developmental Neurobiology, King's College London, Guy's Campus, London, United Kingdom.
Ian D ThompsonMRC Centre for Developmental Neurobiology, King's College London, Guy's Campus, London, United Kingdom.

Funding

Medical Research CouncilWellcome TrustWellcome Trust 083205
6 · The paper itself

Abstract

The mouse dorsal lateral geniculate nucleus (dLGN) is an intermediary between retina and primary visual cortex (V1). Recent investigations are beginning to reveal regional complexity in mouse dLGN. Using local injections of retrograde tracers into V1 of adult and neonatal mice, we examined the developing organisation of geniculate projection columns: the population of dLGN-V1 projection neurons that converge in cortex. Serial sectioning of the dLGN enabled the distribution of labelled projection neurons to be reconstructed and collated within a common standardised space. This enabled us to determine: the organisation of cells within the dLGN-V1 projection columns; their internal organisation (topology); and their order relative to V1 (topography). Here, we report parameters of projection columns that are highly variable in young animals and refined in the adult, exhibiting profiles consistent with shell and core zones of the dLGN. Additionally, such profiles are disrupted in adult animals with reduced correlated spontaneous activity during development. Assessing the variability between groups with partial least squares regression suggests that 4-6 cryptic lamina may exist along the length of the projection column. Our findings further spotlight the diversity of the mouse dLGN--an increasingly important model system for understanding the pre-cortical organisation and processing of visual information. Furthermore, our approach of using standardised spaces and pooling information across many animals will enhance future functional studies of the dLGN.

Indexed as

AnimalsAxonal TransportFemaleFluorescent DyesGeniculate BodiesImaging, Three-DimensionalMagnetic Resonance ImagingMaleMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicNeuronsReceptors, NicotinicRetinal Ganglion CellsThalamusFluorescent DyesReceptors, Nicotinic

Identifiers

PMID26727264
PMCPMC4699701

What OpenQuestion holds

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LicenceCC BY
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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.