Evidence map›Paper›PMID 25618335›Full record

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

High content screening for modulators of cardiac differentiation in human pluripotent stem cells.

Sean Spiering, Herman Davidovics, Paul J Bushway, Mark Mercola, Erik Willems

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. Frontiers in pharmacology · 2019
    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.

Sean SpieringMuscle Development and Regeneration Program, Sanford-Burnham Medical Research Institute, 10901 North Torrey Pines Road, La Jolla, CA, 92037, USA.
Herman Davidovics
Paul J Bushway
Mark Mercola
Erik Willems

Funding

Tumor Microenvironment and Cancer ImmunologyP30CA030199 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI Michael Jackson · 1985 to 2026
$107.2M
Project 4: A Developmental Perspective to Nitrosative/Oxidative SusceptibilityP01ES016738 · NIEHS · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI RIEDL, STEFAN J · 2008 to 2012
$8.5M
Project-002P30NS076411 · NINDS · SCINTILLON INSTITUTE FOR PHOTOBIOLOGY · PI LIPTON, STUART A · 2011 to 2016
$4.5M
microRNAs and Integrative Control on Cardiopoiesis - CHANGE OF GRANTEE INSTITUTIOR01HL113601 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MERCOLA, MARK · 2012 to 2016
$2.2M
Myocardial Angiogenesis and CardioprotectionR01HL108176 · NHLBI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI MERCOLA, MARK · 2012 to 2015
$1.9M
Endothelial hiPSC-Cardiomyocyte Interactions Relevant to Model Disease and AgingR21AG043917 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MERCOLA, MARK · 2013 to 2014
$486k
NCI NIH HHS P30 CA030199NHLBI NIH HHS HL108176NHLBI NIH HHS HL113601NHLBI NIH HHS R01 HL108176NHLBI NIH HHS R01 HL113601NIA NIH HHS AG043917NIA NIH HHS R21 AG043917NIEHS NIH HHS P01 ES016738NINDS NIH HHS P30 NS076411
6 · The paper itself

Abstract

Chemical genomics has the unique potential to expose novel mechanisms of complex cellular biology through screening of small molecules in in vitro assays of a biological phenotype of interest, followed by target identification. In the case of disease-specific assays, the cellular proteins identified might constitute novel drug targets, and the small molecules themselves might be developed as drug leads. In cardiovascular biology, a chemical genomics approach to study the formation of cardiomyocyte, vascular endothelial, and smooth muscle lineages might contribute to therapeutic regeneration. Here, we describe methods used to develop high content screening assays implementing multipotent cardiovascular progenitors derived from human pluripotent stem cells and have identified novel compounds that direct cardiac differentiation.

Indexed as

High-Throughput Screening AssaysBasic Helix-Loop-Helix ProteinsCell Culture TechniquesCell DifferentiationCell LineCell SeparationDrug Evaluation, PreclinicalHumansInduced Pluripotent Stem CellsMyocytes, CardiacPhenotypePluripotent Stem CellsReceptor, Platelet-Derived Growth Factor alphaBasic Helix-Loop-Helix ProteinsMESP1 protein, humanReceptor, Platelet-Derived Growth Factor alpha

Identifiers

PMID25618335
PMCPMC4766105

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.