Evidence map›Paper›PMID 39726164›Full record

ArticleJournal of anatomy2025

Histological analysis of retinal development and remodeling in the brown anole lizard (Anolis sagrei).

Ashley M Rasys, Shana H Pau, Katherine E Irwin, Sherry Luo, Hannah Q Kim, M Austin Wahle, Douglas B Menke, James D Lauderdale

Abstract read
In one paragraph

Article in Journal of anatomy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Convergent re-evolution of CNS structures: focus on the fovea.Current opinion in genetics & development · 2026
    Review
  3. Article
  4. Review
  5. 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

8 authors.

Ashley M RasysDepartment of Cellular Biology, The University of Georgia, Athens, Georgia, USA.
Shana H PauDepartment of Genetics, The University of Georgia, Athens, Georgia, USA.
Katherine E IrwinDepartment of Cellular Biology, The University of Georgia, Athens, Georgia, USA.
Sherry LuoDepartment of Genetics, The University of Georgia, Athens, Georgia, USA.
Hannah Q KimDepartment of Cellular Biology, The University of Georgia, Athens, Georgia, USA.
M Austin WahleDepartment of Genetics, The University of Georgia, Athens, Georgia, USA.
Douglas B MenkeDepartment of Genetics, The University of Georgia, Athens, Georgia, USA.
James D LauderdaleDepartment of Cellular Biology, The University of Georgia, Athens, Georgia, USA.ORCID 0000-0001-7503-0528

Funding

T32 Predoctoral training grant in geneticsT32GM007103 · NIGMS · UNIVERSITY OF GEORGIA (UGA) · PI DYER, KELLY A · 1985 to 2021
$5.9M
Achievement Rewards for College Scientists FoundationARCS Foundation ScholarshipNational Science Foundation 1149453National Science Foundation 1827647NIGMS NIH HHS T32 GM007103NIGMS NIH HHS T32GM007103Society for Developmental Biology Emerging Models
6 · The paper itself

Abstract

The fovea, a pit in the retina, is crucial for high-acuity vision in humans and is found in the eyes of other vertebrates, including certain primates, birds, lizards, and fish. Despite its importance for vision, our understanding of the mechanisms involved in fovea development remains limited. Widely used ocular research models lack a foveated retina, and studies on fovea development are mostly limited to histological and molecular studies in primates. As a first step toward elucidating fovea development in nonprimate vertebrates, we present a detailed histological atlas of retina and fovea development in the bifoveated Anolis sagrei lizard, a novel reptile model for fovea research. We test the hypothesis that retinal remodeling, leading to fovea formation and photoreceptor cell packing, is related to asymmetric changes in eye shape. Our findings show that anole retina development follows the typical spatiotemporal patterning observed in most vertebrates: retinal neurogenesis starts in the central retina, progresses through the temporal retina, and finishes in the nasal retina. However, the areas destined to become the central or temporal fovea differentiate earlier than the rest of the retina. We observe dynamic changes in retinal thickness during ocular elongation and retraction-thinning during elongation and thickening during retraction. Additionally, a transient localized thickening of the ganglion cell layer occurs in the temporal fovea region just before pit formation. Our data indicate that anole retina development is similar to that of humans, including the onset and progression of retinal neurogenesis, followed by changes in ocular shape and retinal remodeling leading to pit formation. We propose that anoles are an excellent model system for fovea development research.

Indexed as

Fovea CentralisLizardsRetinaAnimalsfovealizardneurogenesisretinal remodelingspatiotemporal patterning

Identifiers

PMID39726164
PMCPMC12079762

What Socratic holds

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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 Socratic graph.