Evidence map›Paper›PMID 26702142›Full record

ReviewAmerican journal of physiology. Heart and circulatory physiology2016

The role of microRNAs in cardiac development and regenerative capacity.

Michael G Katz, Anthony S Fargnoli, Andrew P Kendle, Roger J Hajjar, Charles R Bridges

Abstract readReview
In one paragraph

Review in American journal of physiology. Heart and circulatory physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

36 citing papers in PubMed, 64 citations in OpenAlex.

  1. Review
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  7. Article
  8. Article
  9. Cardiac microRNAs: diagnostic and therapeutic potential.Archives of medical science : AMS · 2023
    Article
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  11. Review
  12. Article
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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 at 2 institutions in 1 country.

Michael G KatzSanger Heart & Vascular Institute, Carolinas HealthCare System, Charlotte, North Carolina; and Cardiovascular Research Center, Mount Sinai School of Medicine, New York, New York.
Anthony S FargnoliSanger Heart & Vascular Institute, Carolinas HealthCare System, Charlotte, North Carolina; and.
Andrew P KendleSanger Heart & Vascular Institute, Carolinas HealthCare System, Charlotte, North Carolina; and.
Roger J HajjarCardiovascular Research Center, Mount Sinai School of Medicine, New York, New York.
Charles R BridgesSanger Heart & Vascular Institute, Carolinas HealthCare System, Charlotte, North Carolina; and crbridges99@gmail.com.
Carolinas Healthcare System · USIcahn School of Medicine at Mount Sinai · US

Funding

Translational Studies in Heart Failure Gene TherapyR01HL083078 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI BRIDGES, CHARLES R · 2007 to 2018
$9.2M
Targeting Abnormal Calcium Cycling Using Novel Gene Therapy VectorsR01HL119046 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI AKAR, FADI GABRIEL, HAJJAR, ROGER J. · 2014 to 2017
$2.9M
Role of miR25 in Heart FailureR01HL128072 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HAJJAR, ROGER J., MERCOLA, MARK · 2015 to 2018
$2.5M
NHLBI NIH HHS 5R01-HL-083078-08NHLBI NIH HHS R01 HL083078NHLBI NIH HHS R01 HL119046NHLBI NIH HHS R01 HL128072
6 · The paper itself

Abstract

The mammalian heart has long been considered to be a postmitotic organ. It was thought that, in the postnatal period, the heart underwent a transition from hyperplasic growth (more cells) to hypertrophic growth (larger cells) due to the conversion of cardiomyocytes from a proliferative state to one of terminal differentiation. This hypothesis was gradually disproven, as data were published showing that the myocardium is a more dynamic tissue in which cardiomyocyte karyokinesis and cytokinesis produce new cells, leading to the hyperplasic regeneration of some of the muscle mass lost in various pathological processes. microRNAs have been shown to be critical regulators of cardiomyocyte differentiation and proliferation and may offer the novel opportunity of regenerative hyperplasic therapy. Here we summarize the relevant processes and recent progress regarding the functions of specific microRNAs in cardiac development and regeneration.

Indexed as

RegenerationAnimalsCell DifferentiationCell ProliferationCellular ReprogrammingGene Expression Regulation, DevelopmentalHeart FailureHumansMicroRNAsMorphogenesisMyocardial InfarctionMyocardiumSignal TransductionMicroRNAscardiac regenerationheart developmentheart failuremicroRNAmyocardial infarction

Identifiers

PMID26702142
PMCPMC4796601
OpenAlexW2282999253

What OpenQuestion holds

Textmetadata
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.