Evidence map›Paper›PMID 38543122›Full record

ReviewPharmaceuticals (Basel, Switzerland)2024

Differentiation of Pluripotent Stem Cells for Disease Modeling: Learning from Heart Development.

Congwu Chi, Truman J Roland, Kunhua Song

Open access · goldAbstract readReview
In one paragraph

Review in Pharmaceuticals (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Genes & diseases · 2026
    Article
  2. Review
  3. Review
  4. Frontiers in cell and developmental biology · 2024
    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 at 1 institution in 1 country.

Congwu ChiHeart Institute, University of South Florida, Tampa, FL 33602, USA.
Truman J RolandHeart Institute, University of South Florida, Tampa, FL 33602, USA.ORCID 0009-0001-0927-9816
Kunhua SongHeart Institute, University of South Florida, Tampa, FL 33602, USA.ORCID 0000-0003-3805-4509
University of South Florida · US

Funding

Mechanisms for cell signaling in the control of cardiomyogenesisR01HL133230 · NHLBI · UNIVERSITY OF SOUTH FLORIDA · PI Kunhua Song · 2016 to 2026
$4.2M
Regulation of gene transcription and alternative splicing by a long non-coding RNAR01HL159086 · NHLBI · UNIVERSITY OF SOUTH FLORIDA · PI SONG, KUNHUA, VONDRISKA, THOMAS M. · 2022 to 2025
$2.1M
NHLBI NIH HHS R01 HL133230NHLBI NIH HHS R01 HL159086
6 · The paper itself

Abstract

Heart disease is a pressing public health problem and the leading cause of death worldwide. The heart is the first organ to gain function during embryogenesis in mammals. Heart development involves cell determination, expansion, migration, and crosstalk, which are orchestrated by numerous signaling pathways, such as the Wnt, TGF-β, IGF, and Retinoic acid signaling pathways. Human-induced pluripotent stem cell-based platforms are emerging as promising approaches for modeling heart disease in vitro. Understanding the signaling pathways that are essential for cardiac development has shed light on the molecular mechanisms of congenital heart defects and postnatal heart diseases, significantly advancing stem cell-based platforms to model heart diseases. This review summarizes signaling pathways that are crucial for heart development and discusses how these findings improve the strategies for modeling human heart disease in vitro.

Indexed as

cardiac differentiationdisease modelingheart developmentpluripotent stem cellssignaling pathways

Identifiers

PMID38543122
PMCPMC10975450
OpenAlexW4392471507

What Socratic 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 Socratic graph.