Evidence map›Paper›PMID 32471864›Full record

ArticleDisease models & mechanisms2020

Silencing of CCR4-NOT complex subunits affects heart structure and function.

Lisa Elmén, Claudia B Volpato, Anaïs Kervadec, Santiago Pineda, Sreehari Kalvakuri, Nakissa N Alayari, Luisa Foco, Peter P Pramstaller, Karen Ocorr, Alessandra Rossini and 4 more

Open access · goldAbstract read
In one paragraph

Article in Disease models & mechanisms, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

11 citing papers in PubMed, 27 citations in OpenAlex.

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  6. Distinct patterns of gene expression during regeneration and asexual reproduction in the annelid Pristina leidyi.Journal of experimental zoology. Part B, Molecular and developmental evolution · 2022
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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

14 authors at 3 institutions in 2 countries.

Lisa ElménDevelopment Aging and Regeneration Program, Sanford Burnham Prebys Medical Discovery Institute, 10901 N Torrey Pines Rd, La Jolla, CA 92037, USA.
Claudia B VolpatoInstitute for Biomedicine, Eurac Research, Affiliated Institute of the University of Lübeck, Via Galvani 31, 39100 Bolzano, Italy.
Anaïs KervadecDevelopment Aging and Regeneration Program, Sanford Burnham Prebys Medical Discovery Institute, 10901 N Torrey Pines Rd, La Jolla, CA 92037, USA.
Santiago PinedaDevelopment Aging and Regeneration Program, Sanford Burnham Prebys Medical Discovery Institute, 10901 N Torrey Pines Rd, La Jolla, CA 92037, USA.
Sreehari KalvakuriDevelopment Aging and Regeneration Program, Sanford Burnham Prebys Medical Discovery Institute, 10901 N Torrey Pines Rd, La Jolla, CA 92037, USA.
Nakissa N AlayariDevelopment Aging and Regeneration Program, Sanford Burnham Prebys Medical Discovery Institute, 10901 N Torrey Pines Rd, La Jolla, CA 92037, USA.
Luisa FocoInstitute for Biomedicine, Eurac Research, Affiliated Institute of the University of Lübeck, Via Galvani 31, 39100 Bolzano, Italy.
Peter P PramstallerInstitute for Biomedicine, Eurac Research, Affiliated Institute of the University of Lübeck, Via Galvani 31, 39100 Bolzano, Italy.
Karen OcorrDevelopment Aging and Regeneration Program, Sanford Burnham Prebys Medical Discovery Institute, 10901 N Torrey Pines Rd, La Jolla, CA 92037, USA.
Alessandra RossiniInstitute for Biomedicine, Eurac Research, Affiliated Institute of the University of Lübeck, Via Galvani 31, 39100 Bolzano, Italy.
Anthony CammaratoJohns Hopkins University, Division of Cardiology, 720 Rutland Ave., Baltimore, MD 21205, USA.
Alexandre R ColasDevelopment Aging and Regeneration Program, Sanford Burnham Prebys Medical Discovery Institute, 10901 N Torrey Pines Rd, La Jolla, CA 92037, USA.
Andrew A HicksInstitute for Biomedicine, Eurac Research, Affiliated Institute of the University of Lübeck, Via Galvani 31, 39100 Bolzano, Italy rolf@sbpdiscovery.org andrew.hicks@eurac.edu.ORCID 0000-0001-6320-0411
Rolf BodmerDevelopment Aging and Regeneration Program, Sanford Burnham Prebys Medical Discovery Institute, 10901 N Torrey Pines Rd, La Jolla, CA 92037, USA rolf@sbpdiscovery.org andrew.hicks@eurac.edu.ORCID 0000-0001-9087-1210
Sanford Burnham Prebys Medical Discovery Institute · USEurac Research · ITJohns Hopkins University · US

Funding

HEART DEVELOPMENT IN DROSOPHILAR01HL054732 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BODMER, ROLF · 1995 to 2024
$11.3M
PATHOGENESIS AND IN VIVO SUPPRESSION OF THIN FILAMENT-BASED CARDIOMYOPATHIESR01HL124091 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI Anthony Cammarato · 2015 to 2026
$4.3M
Discovery of Small Molecule Promoters of Cardiomyocyte Proliferation to Restore Cardiac Performance in DiseaseR01HL148827 · NHLBI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI COLAS, ALEXANDRE ROMAIN · 2019 to 2022
$2.0M
Cellular/molecular substrates linking channel dysfunction and pathological cardiac remodelingR01HL132241 · NHLBI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI OCORR, KAREN · 2017 to 2020
$1.9M
Discovery of small molecule regulators of atrial cardiomyocyte action potential duration to restore normal cardiac rhythm in atrial fibrillationR01HL153645 · NHLBI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI COLAS, ALEXANDRE ROMAIN · 2021 to 2024
$1.9M
Cellular Mediators of Cardiac Aging and Arrhythmia in DrosophilaR21AG061598 · NIA · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI OCORR, KAREN · 2019 to 2020
$536k
NHLBI NIH HHS R01 HL054732NHLBI NIH HHS R01 HL124091NHLBI NIH HHS R01 HL132241NHLBI NIH HHS R01 HL148827NHLBI NIH HHS R01 HL153645NIA NIH HHS R21 AG061598
6 · The paper itself

Abstract

The identification of genetic variants that predispose individuals to cardiovascular disease and a better understanding of their targets would be highly advantageous. Genome-wide association studies have identified variants that associate with QT-interval length (a measure of myocardial repolarization). Three of the strongest associating variants (single-nucleotide polymorphisms) are located in the putative promotor region of

Indexed as

Gene SilencingAction PotentialsAnimalsAnimals, Genetically ModifiedCell ProliferationDrosophila melanogasterDrosophila ProteinsExoribonucleasesGene Expression Regulation, DevelopmentalGenome-Wide Association StudyHeart RateHeLa CellsHumansInduced Pluripotent Stem CellsIntracellular Signaling Peptides and ProteinsLong QT SyndromeCNOT1 protein, humanCnot4 protein, DrosophilaCNOT7 protein, humanDrosophila ProteinsExoribonucleasesIntracellular Signaling Peptides and ProteinsNOT1 protein, DrosophilaRepressor ProteinsRibonucleasesRNA-Binding ProteinsTranscription Factorstwin protein, DrosophilaArrhythmiaCardiomyocytesCNOT1Drosophila heartGWAShiPSCLong-QT syndrome

Identifiers

PMID32471864
PMCPMC7390626
OpenAlexW3029150811

What OpenQuestion holds

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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.