Evidence map›Paper›PMID 29665410›Full record

ArticleMechanisms of development2018

The role of the Rx homeobox gene in retinal progenitor proliferation and cell fate specification.

H M Rodgers, V J Huffman, V A Voronina, M Lewandoski, P H Mathers

Abstract read
In one paragraph

Article in Mechanisms of development, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Development of Retinal Astroglia.Annual review of vision science · 2025
    Review
  4. Article
  5. Article
  6. Itpka depletion implicates defects in anterior neural development ofFrontiers in cell and developmental biology · 2025
    Article
  7. NMNAT1 Is Essential for Human iPS Cell Differentiation to the Retinal Lineage.Investigative ophthalmology & visual science · 2024
    Article
  8. Article
  9. Prdm15 acts upstream of Wnt4 signaling in anterior neural development ofFrontiers in cell and developmental biology · 2024
    Article
  10. The Ribosomal Protein L5 Functions DuringFrontiers in cell and developmental biology · 2022
    Article
  11. Article
  12. Review
  13. Article
  14. eLife · 2019
    Article
  15. Article
  16. 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 2 institutions in 1 country.

H M RodgersNeuroscience Graduate Program, West Virginia University School of Medicine, Morgantown, WV 26506, United States; Sensory Neuroscience Research Center, West Virginia University School of Medicine, Morgantown, WV 26506, United States.
V J HuffmanSensory Neuroscience Research Center, West Virginia University School of Medicine, Morgantown, WV 26506, United States; Potomac State College of West Virginia University, Keyser, WV 26726, United States; Department of Otolaryngology, West Virginia University School of Medicine, Morgantown, WV 26506, United States.
V A VoroninaSensory Neuroscience Research Center, West Virginia University School of Medicine, Morgantown, WV 26506, United States; Laboratory of Cancer and Developmental Biology, NCI-Frederick, National Institutes of Health, Frederick, MD 21702, United States; Biochemistry and Molecular Biology Graduate Program, West Virginia University School of Medicine, Morgantown, WV 26506, United States.
M LewandoskiLaboratory of Cancer and Developmental Biology, NCI-Frederick, National Institutes of Health, Frederick, MD 21702, United States.
P H MathersSensory Neuroscience Research Center, West Virginia University School of Medicine, Morgantown, WV 26506, United States; Department of Otolaryngology, West Virginia University School of Medicine, Morgantown, WV 26506, United States; Department of Ophthalmology, West Virginia University School of Medicine, Morgantown, WV 26506, United States; Department of Biochemistry, West Virginia University School of Medicine, Morgantown, WV 26506, United States. Electronic address: pmathers@hsc.wvu.edu.
West Virginia University · USFrederick National Laboratory for Cancer Research · US

Funding

WV INBRE: The Inhibitor of Growth Family Member 4 (ING4) inhibits L-Type Amino Acid Transporter 1 (LAT1) expression to suppress Breast CancerP20GM103434 · NIGMS · MARSHALL UNIVERSITY · PI Travis Salisbury · 2012 to 2026
$61.1M
THE ROLE OF HEF1 PROTEIN IN INVASION OF METASTATIC BREAST CANCERP20RR016440 · NCRR · WEST VIRGINIA UNIVERSITY · PI CUFF, CHRISTOPHER F · 2001 to 2010
$22.8M
Structural dynamics of developing auditory circuitsP20RR015574 · NCRR · WEST VIRGINIA UNIVERSITY · PI SPIROU, GEORGE A · 2000 to 2009
$18.1M
West Virginia Flow Cytometry Core FacilityP30GM103488 · NIGMS · WEST VIRGINIA UNIVERSITY · PI GIBSON, LAURA F. · 2012 to 2016
$4.8M
Identification and characterization of FGF target genesZIABC011321 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LEWANDOSKI, MARK B · 2010 to 2025
$4.6M
Molecular control of retinal stem cell developmentR01EY012152 · NEI · WEST VIRGINIA UNIVERSITY · PI MATHERS, PETER H · 2005 to 2007
$968k
MOLECULAR CONTROL OF RETINAL STEM CELL DEVELOPMENTR29EY012152 · NEI · WEST VIRGINIA UNIVERSITY · PI MATHERS, PETER H · 1998 to 2002
$316k
NCRR NIH HHS P20 RR015574NCRR NIH HHS P20 RR016440NEI NIH HHS R01 EY012152NEI NIH HHS R29 EY012152NIGMS NIH HHS P20 GM103434NIGMS NIH HHS P30 GM103488
6 · The paper itself

Abstract

The Retinal homeobox gene (Rx; also Rax) plays a crucial role in the early development of the vertebrate eye. Germline deletion of Rx in mice results in the failure of optic vesicle formation, leading to anophthalmia. Recent research using conditional mouse knockout models provides some clues to the role of Rx in eye development following optic vesicle formation. However, the functions of Rx in embryonic retinogenesis are still not fully understood. We investigated the function of Rx in the mouse neural retina using a conditional knockout where the Pax6α-Cre driver deletes Rx activity in early retinal progenitors. The deletion of Rx activity causes a loss of retinal lamination, a depletion of retinal progenitors, and a change in retinal cell fate in our conditional knockout model. The deletion of Rx leads to an absence of late-born retinal neurons (rods and bipolar cells) and Müller glia at postnatal ages, as well as a loss of the early-born cone photoreceptors. Decreased BrdU labeling in the Rx-deleted portion of the retina suggests a loss of retinal progenitors via early cell cycle exit, which likely prevents the formation of late-born cells. As early-born cells, cone photoreceptors should not be as affected by early cell cycle exit of retinal progenitors. However, embryonic cone photoreceptor labeling is also markedly reduced in Rx-deleted retinas. Together these data demonstrate the importance of Rx for retinal progenitor proliferation and a specific requirement of Rx for cone formation in mice.

Indexed as

AnimalsAnophthalmosCell CycleCell DifferentiationCell ProliferationDisease Models, AnimalEye ProteinsGene Expression Regulation, DevelopmentalHomeodomain ProteinsHumansMiceMice, KnockoutRetinaRetinal Cone Photoreceptor CellsStem CellsEye ProteinsHomeodomain ProteinsRx protein, mouse

Identifiers

PMID29665410
PMCPMC5972075
OpenAlexW2798040129

What OpenQuestion holds

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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.