Evidence map›Paper›PMID 24699247›Full record

ArticlePloS one2014

Rax-CreERT2 knock-in mice: a tool for selective and conditional gene deletion in progenitor cells and radial glia of the retina and hypothalamus.

Thomas Pak, Sooyeon Yoo, Ana L Miranda-Angulo, Ana M Miranda-Angulo, Hong Wang, Seth Blackshaw

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

49 citing papers in PubMed, 70 citations in OpenAlex.

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  6. Variable transduction of thyroid hormone signaling in structures of the mouse brain.Proceedings of the National Academy of Sciences of the United States of America · 2025
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4 · The record

Corrections and comments

  • Erratum issued
    Miranda-Angulo, Ana M [corrected to Miranda-Angulo, Ana L]
5 · Who and what money

Authors and funding

6 authors at 4 institutions in 2 countries.

Thomas PakDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Sooyeon YooDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Ana L Miranda-Angulo
Ana M Miranda-AnguloDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America; Institute of Medical Research, School of Medicine, Universidad de Antioquia, Medellín, Colombia.
Hong WangDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Seth BlackshawDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America; Department of Ophthalmology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America; Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America; Center for High-Throughput Biology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America; Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Johns Hopkins Medicine · USHigh Throughput Biology (United States) · USJohns Hopkins University · USUniversidad de Antioquia · CO

Funding

Murine Mutagenesis CoreP30NS050274 · NINDS · JOHNS HOPKINS UNIVERSITY · PI KOLODKIN, ALEX L · 2005 to 2020
$10.9M
Transcriptional regulation of retinal cell differentiation and functionR01EY020560 · NEI · JOHNS HOPKINS UNIVERSITY · PI BLACKSHAW, SETH · 2011 to 2021
$4.4M
Genetic analysis of hypothalamic tanycyte functionR21NS067393 · NINDS · JOHNS HOPKINS UNIVERSITY · PI BLACKSHAW, SETH · 2009 to 2010
$449k
NEI NIH HHS R01 EY020560NINDS NIH HHS P30 NS050274NINDS NIH HHS R21 NS067393NINDS NIH HHS R21NS067393
6 · The paper itself

Abstract

To study gene function in neural progenitors and radial glia of the retina and hypothalamus, we developed a Rax-CreERT2 mouse line in which a tamoxifen-inducible Cre recombinase is inserted into the endogenous Rax locus. By crossing Rax-CreER(T2) with the Cre-dependent Ai9 reporter line, we demonstrate that tamoxifen-induced Cre activity recapitulates the endogenous Rax mRNA expression pattern. During embryonic development, Cre recombinase activity in Rax-CreER(T2) is confined to retinal and hypothalamic progenitor cells, as well as progenitor cells of the posterior pituitary. At postnatal time points, selective Cre recombinase activity is seen in radial glial-like cell types in these organs--specifically Müller glia and tanycytes--as well as pituicytes. We anticipate that this line will prove useful for cell lineage analysis and investigation of gene function in the developing and mature retina, hypothalamus and pituitary.

Indexed as

Gene DeletionAnimalsAntineoplastic Agents, HormonalBlotting, SouthernCell LineageEye ProteinsFemaleHomeodomain ProteinsHypothalamusImmunoenzyme TechniquesIntegrasesMaleMiceMice, Inbred C57BLMice, TransgenicNeurogliaAntineoplastic Agents, HormonalCre recombinaseEye ProteinsHomeodomain ProteinsIntegrasesRax protein, mouseReceptors, EstrogenRNA, MessengerTamoxifenTranscription Factors

Identifiers

PMID24699247
PMCPMC3974648
OpenAlexW1981117734

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.