Evidence map›Paper›PMID 24567220›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2014

Multicolor labeling in developmental gene regulatory network analysis.

Aditya J Sethi, Robert C Angerer, Lynne M Angerer

Abstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
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  9. Analysis of microRNA functions.Methods in cell biology · 2019
    Review
  10. Article
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  12. Article
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  15. 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

3 authors.

Aditya J SethiNational Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA.
Robert C Angerer
Lynne M Angerer

Funding

Molecular mechanisms of cell fate specificationZIADE000712 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI ANGERER, ROBERT · 2009 to 2017
$6.8M
Intramural NIH HHS ZIA DE000712
6 · The paper itself

Abstract

The sea urchin embryo is an important model system for developmental gene regulatory network (GRN) analysis. This chapter describes the use of multicolor fluorescent in situ hybridization (FISH) as well as a combination of FISH and immunohistochemistry in sea urchin embryonic GRN studies. The methods presented here can be applied to a variety of experimental settings where accurate spatial resolution of multiple gene products is required for constructing a developmental GRN.

Indexed as

Gene Regulatory NetworksAnimalsBlastulaFluorescent DyesGene Expression Regulation, DevelopmentalIn Situ Hybridization, FluorescenceSea UrchinsStaining and LabelingTissue FixationFluorescent Dyes

Identifiers

PMID24567220
PMCPMC4609530

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.