Evidence map›Paper›PMID 25618332›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2015

Identification of therapeutic small-molecule leads in cultured cells using multiplexed pathway reporter readouts.

Ozlem Kulak, Kiyoshi Yamaguchi, Lawrence Lum

Abstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Zebrafish small molecule screens: Taking the phenotypic plunge.Computational and structural biotechnology journal · 2016
    Review
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.

Ozlem KulakDepartment of Cell Biology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd. NL07.138B, Dallas, TX, 75390-9039, USA.
Kiyoshi Yamaguchi
Lawrence Lum

Funding

Chemical disruption of Wnt-mediated signal transductionR01CA168761 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI KIM, JAMES · 2013 to 2017
$2.3M
NCI NIH HHS R01 CA168761
6 · The paper itself

Abstract

The rapid expansion of molecular screening libraries in size and complexity in the last decade has outpaced the discovery rate of cost-effective strategies to single out reagents with sought-after cellular activities. In addition to representing high-priority therapeutic targets, intensely studied cell signaling systems encapsulate robust reference points for mapping novel chemical activities given our deep understanding of the molecular mechanisms that support their activity. In this chapter, we describe strategies for using transcriptional reporters of several well-interrogated signal transduction pathways coupled with high-throughput biochemical assays to fingerprint novel compounds for drug target identification agendas.

Indexed as

Gene ExpressionGenes, ReporterHigh-Throughput Screening AssaysSmall Molecule LibrariesCell LineCells, CulturedDrug Evaluation, PreclinicalHumansLuciferasesLuminescent MeasurementsSignal TransductionTransfectionLuciferasesSmall Molecule Libraries

Identifiers

PMID25618332
PMCPMC4313378

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.