Evidence map›Paper›PMID 29956448›Full record

ArticleGenesis (New York, N.Y. : 2000)2018

Tracking neural crest cell cycle progression in vivo.

Sriivatsan G Rajan, Kristin L Gallik, James R Monaghan, Rosa A Uribe, Marianne E Bronner, Ankur Saxena

Open access · greenAbstract read
In one paragraph

Article in Genesis (New York, N.Y. : 2000), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

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  14. The motif EThe Journal of biological chemistry · 2020
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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 at 4 institutions in 1 country.

Sriivatsan G RajanDepartment of Biological Sciences, University of Illinois at Chicago, Chicago, Illinois, 60607.
Kristin L GallikDepartment of Biological Sciences, University of Illinois at Chicago, Chicago, Illinois, 60607.
James R MonaghanDepartment of Biology, Northeastern University, Boston, Massachusetts, 02131.
Rosa A UribeDepartment of Biosciences, Rice University, Houston, Texas, 77005.
Marianne E BronnerDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, California, 91125.
Ankur SaxenaDepartment of Biological Sciences, University of Illinois at Chicago, Chicago, Illinois, 60607.ORCID http://orcid.org/0000-0001-8646-2887
University of Illinois Chicago · USCalifornia Institute of Technology · USNortheastern University · USRice University · US

Funding

Gene Regulatory Network Controlling Premigratory Cranial vs Trunk Neural CrestR01DE024157 · NIDCR · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI BRONNER, MARIANNE · 2014 to 2025
$4.0M
Functional analysis of early vagal neural crest and ENS developmentF32HD080343 · NICHD · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI URIBE, ROSA A · 2014 to 2016
$164k
NICHD NIH HHS F32 HD080343NIDCR NIH HHS R01 DE024157
6 · The paper itself

Abstract

Analysis of cell cycle entry/exit and progression can provide fundamental insights into stem cell propagation, maintenance, and differentiation. The neural crest is a unique stem cell population in vertebrate embryos that undergoes long-distance collective migration and differentiation into a wide variety of derivatives. Using traditional techniques such as immunohistochemistry to track cell cycle changes in such a dynamic population is challenging, as static time points provide an incomplete spatiotemporal picture. In contrast, the fluorescent, ubiquitination-based cell cycle indicator (Fucci) system provides in vivo readouts of cell cycle progression and has been previously adapted for use in zebrafish. The most commonly used Fucci systems are ubiquitously expressed, making tracking of a specific cell population challenging. Therefore, we generated a transgenic zebrafish line, Tg(-4.9sox10:mAG-gmnn(1/100)-2A-mCherry-cdt1(1/190)), in which the Fucci system is specifically expressed in delaminating and migrating neural crest cells. Here, we demonstrate validation of this new tool and its use in live high-resolution tracking of cell cycle progression in the neural crest and derivative populations.

Indexed as

AnimalsAnimals, Genetically ModifiedCell CycleCell DifferentiationCell MovementCell TrackingGenetic EngineeringLuminescent ProteinsMicroscopy, FluorescenceNeural CrestZebrafishZebrafish ProteinsLuminescent ProteinsZebrafish ProteinsFucciSox10zebrafish

Identifiers

PMID29956448
PMCPMC6143351
OpenAlexW2811474557

What OpenQuestion holds

Textmetadata
LicenceTDM
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.