Evidence map›Paper›PMID 38076903›Full record

ArticleResearch square2023

Pharmacological or genetic inhibition of LTCC promotes cardiomyocyte proliferation through inhibition of calcineurin activity.

Lynn A C Devilée, Jessica M Miller, Janice D Reid, Abou Bakr M Salama, Qinghui Ou, Madiha Jamal, Yibing Nong, Douglas Andres, Jonathan Satin, Tamer M A Mohamed and 2 more

Open access · greenAbstract readPreprint
In one paragraph

Article in Research square, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 4 countries.

Lynn A C DeviléeQIMR Berghofer Medical Research Institute, Cardiac Bioengineering Laboratory, Brisbane, Queensland, Australia.ORCID 0000-0002-6176-4392
Jessica M MillerInstitute of Molecular Cardiology, Department of Medicine, University of Louisville, KY, U.S.A.
Janice D ReidQIMR Berghofer Medical Research Institute, Cardiac Bioengineering Laboratory, Brisbane, Queensland, Australia.
Abou Bakr M SalamaInstitute of Molecular Cardiology, Department of Medicine, University of Louisville, KY, U.S.A.ORCID 0000-0002-2241-3792
Qinghui OuInstitute of Molecular Cardiology, Department of Medicine, University of Louisville, KY, U.S.A.
Madiha JamalInstitute of Molecular Cardiology, Department of Medicine, University of Louisville, KY, U.S.A.
Yibing NongCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, Department of Medicine, University of Louisville, Louisville, KY, U.S.A.
Douglas AndresDepartment of Molecular and Cellular Biochemistry, University of Kentucky College of Medicine, Lexington, KY, U.S.A.
Jonathan SatinDepartment of Physiology, University of Kentucky College of Medicine, Lexington, KY, U.S.A.
Tamer M A MohamedInstitute of Molecular Cardiology, Department of Medicine, University of Louisville, KY, U.S.A.
James E HudsonQIMR Berghofer Medical Research Institute, Cardiac Bioengineering Laboratory, Brisbane, Queensland, Australia.ORCID 0000-0003-0832-9356
Riham R E AbouleisaInstitute of Molecular Cardiology, Department of Medicine, University of Louisville, KY, U.S.A.ORCID 0000-0001-8883-068X
Baylor College of Medicine · USQIMR Berghofer Medical Research Institute · AUUniversity of Louisville Hospital · USAlfaisal University · SABioengineering Center · RUUniversity of Kentucky · US

Funding

TBDP30GM127607 · NIGMS · UNIVERSITY OF LOUISVILLE · PI JONES, STEVEN P · 2018 to 2022
$6.3M
Induction of Cardiomyocyte Proliferation via Transient Expression of Cell Cycle Factors as a Promising Therapy for Heart FailureR01HL147921 · NHLBI · UNIVERSITY OF LOUISVILLE · PI Tamer M A Mohamed, Jonathan Satin · 2020 to 2026
$5.3M
Defining the major signaling mechanism which controls spontaneous cardiomyocyte proliferation in the Neonatal StageR01HL178610 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI Tamer M A Mohamed · 2025 to 2026
$1.5M
Triple Gene Therapy for Ischemic Heart FailureR61HL177472 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI MOHAMED, TAMER M A, ROSENGART, TODD K · 2025 to 2025
$560k
Deciphering the Relationship Between Cardiomyocyte Metabolic Configuration and Cell Cycle Re-entryF32HL149140 · NHLBI · UNIVERSITY OF LOUISVILLE · PI ABOULEISA, RIHAM RAAFAT ELGHARIB · 2020 to 2023
$243k
NHLBI NIH HHS F32 HL149140NHLBI NIH HHS R01 HL147921NHLBI NIH HHS R01 HL178610NHLBI NIH HHS R61 HL177472NIGMS NIH HHS P30 GM127607
6 · The paper itself

Abstract

Cardiomyocytes (CMs) lost during ischemic cardiac injury cannot be replaced due to their limited proliferative capacity, which leads to progressive heart failure. Calcium (Ca

Indexed as

calcineurinCalciumCardiomyocyte proliferationCell cycleLTCCRRAD

Identifiers

PMID38076903
PMCPMC10705701
OpenAlexW4389175383

What OpenQuestion 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 OpenQuestion graph.