Evidence map›Paper›PMID 29440224›Full record

ReviewGenes & development2018

Competent for commitment: you've got to have heart!

Rajan Jain, Jonathan A Epstein

Abstract readReview
In one paragraph

Review in Genes & development, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. In-Depth Genomic Analysis: The New Challenge in Congenital Heart Disease.International journal of molecular sciences · 2024
    Review
  3. Genomic frontiers in congenital heart disease.Nature reviews. Cardiology · 2022
    Review
  4. Three-dimensional chromatin organization in cardiac development and disease.Journal of molecular and cellular cardiology · 2021
    Review
  5. Review
  6. Article
  7. Article
  8. Early lineage specification defines alveolar epithelial ontogeny in the murine lung.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  9. Integrative regulation of physiology by histone deacetylase 3.Nature reviews. Molecular cell biology · 2019
    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

2 authors.

Rajan JainDepartment of Medicine, Department of Cell and Developmental Biology, Institute for Regenerative Medicine, Penn Cardiovascular Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.ORCID 0000-0002-1979-044X
Jonathan A EpsteinDepartment of Medicine, Department of Cell and Developmental Biology, Institute for Regenerative Medicine, Penn Cardiovascular Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.

Funding

An unusual homeobox gene required for heart developmentR01HL071546 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI EPSTEIN, JONATHAN A. · 2003 to 2017
$4.9M
The role of nuclear architecture in cardiac developmentR01HL131611 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI EPSTEIN, JONATHAN A. · 2016 to 2017
$804k
Investigating the role of Hopx in cardiac progenitor proliferationK08HL119553 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI JAIN, RAJAN · 2013 to 2017
$741k
NHLBI NIH HHS K08 HL119553NHLBI NIH HHS R01 HL071546NHLBI NIH HHS R01 HL131611
6 · The paper itself

Abstract

The mature heart is composed primarily of four different cell types: cardiac myocytes, endothelium, smooth muscle, and fibroblasts. These cell types derive from pluripotent progenitors that become progressively restricted with regard to lineage potential, giving rise to multipotent cardiac progenitor cells and, ultimately, the differentiated cell types of the heart. Recent studies have begun to shed light on the defining characteristics of the intermediary cell types that exist transiently during this developmental process and the extrinsic and cell-autonomous factors that influence cardiac lineage decisions and cellular competence. This information will shape our understanding of congenital and adult cardiac disease and guide regenerative therapeutic approaches. In addition, cardiac progenitor specification can serve as a model for understanding basic mechanisms regulating the acquisition of cellular identity. In this review, we present the concept of "chromatin competence" that describes the potential for three-dimensional chromatin organization to function as the molecular underpinning of the ability of a progenitor cell to respond to inductive lineage cues and summarize recent studies advancing our understanding of cardiac cell specification, gene regulation, and chromatin organization and how they impact cardiac development.

Indexed as

AnimalsCell LineageChromatinGene Expression Regulation, DevelopmentalHeartHumansMyocardiumNuclear Pore Complex ProteinsStem CellsTranscription FactorsChromatinNuclear Pore Complex ProteinsTranscription Factorscardiac progenitor cellsgene regulationlineage restrictionnuclear architecture

Identifiers

PMID29440224
PMCPMC5828393

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.