Evidence map›Paper›PMID 29079565›Full record

ArticleJournal of the American Heart Association2017

Essentiality of Regulator of G Protein Signaling 6 and Oxidized Ca

Bandana Chakravarti, Jianqi Yang, Katelin E Ahlers-Dannen, Zili Luo, Heather A Flaherty, David K Meyerholz, Mark E Anderson, Rory A Fisher

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

15 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. G protein regulation by RGS proteins in the pathophysiology of dilated cardiomyopathy.American journal of physiology. Heart and circulatory physiology · 2025
    Review
  5. Article
  6. A perspective on Notch signalling in progression and arrhythmogenesis in familial hypertrophic and dilated cardiomyopathies.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2023
    Review
  7. Article
  8. Article
  9. CaInternational journal of molecular sciences · 2022
    Article
  10. Review
  11. Article
  12. Endothelial CaInternational journal of molecular sciences · 2019
    Review
  13. Article
  14. Article
  15. Article
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

8 authors at 3 institutions in 1 country.

Bandana ChakravartiDepartment of Pharmacology, University of Iowa Carver College of Medicine, Iowa City, IA.
Jianqi YangDepartment of Pharmacology, University of Iowa Carver College of Medicine, Iowa City, IA.
Katelin E Ahlers-DannenDepartment of Pharmacology, University of Iowa Carver College of Medicine, Iowa City, IA.
Zili LuoDepartment of Pharmacology, University of Iowa Carver College of Medicine, Iowa City, IA.
Heather A FlahertyDepartment of Veterinary Pathology, Iowa State University, Ames, IA.
David K MeyerholzDepartment of Pathology, University of Iowa Carver College of Medicine, Iowa City, IA.
Mark E AndersonDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.
Rory A FisherDepartment of Pharmacology, University of Iowa Carver College of Medicine, Iowa City, IA rory-fisher@uiowa.edu.
University of Iowa · USIowa State University · USJohns Hopkins University · US

Funding

VASOPRESSIN IN CARDIOVASCULAR REGULATIONP01HL014388 · NHLBI · UNIVERSITY OF IOWA · PI ABBOUD, FRANCOIS M · 1985 to 2018
$40.3M
Mitochondrial Calmodulin Kinase II in Physiology and DiseaseR01HL070250 · NHLBI · VANDERBILT UNIVERSITY · PI ANDERSON, MARK E · 2002 to 2017
$5.2M
CaMKII in Sinus Node Physiology and DiseaseR01HL096652 · NHLBI · UNIVERSITY OF IOWA · PI ANDERSON, MARK E · 2009 to 2016
$3.0M
Molecular Analysis and Role of RGS6 as a Novel Growth SuppressorR01CA161882 · NCI · UNIVERSITY OF IOWA · PI FISHER, RORY A. · 2012 to 2016
$1.5M
NCI NIH HHS R01 CA161882NHLBI NIH HHS P01 HL014388NHLBI NIH HHS R01 HL070250NHLBI NIH HHS R01 HL096652
6 · The paper itself

Abstract

backgroundCongenital heart defects are the most common birth defects worldwide. Although defective Notch signaling is the major cause of mouse embryonic death from cardiovascular defects, how Notch signaling is regulated during embryonic vasculogenesis and heart development is poorly understood. METHODS AND

resultsRegulator of G protein signaling 6 (RGS6)

conclusionsRGS6 and oxidized CaMKIIδ together function as novel critical upstream modulators of Notch signaling required for normal cardiovascular development and embryo survival. Their combined need indicates that they function in parallel pathways needed for Notch1 signaling in yolk sac, placenta and embryos. Thus, dysregulated embryonic RGS6 expression and oxidative activation of CaMKII may potentially contribute to congenital heart defects.

Indexed as

HeartAnimalsBlood VesselsCalcium-Calmodulin-Dependent Protein Kinase Type 2Cell DifferentiationCells, CulturedEnzyme ActivationGene Expression Regulation, DevelopmentalGene Expression Regulation, EnzymologicGenotypeGestational AgeHeart Defects, CongenitalMice, Inbred C57BLMice, KnockoutMorphogenesisOxidation-ReductionCalcium-Calmodulin-Dependent Protein Kinase Type 2Camk2g protein, mouseReactive Oxygen SpeciesReceptors, NotchRgs6 protein, mouseRGS Proteinscardiovascular developmentembryonic lethalityNotch signalingoxidized Ca2+/calmodulin‐dependent protein kinase IIRegulator of G protein signaling 6

Identifiers

PMID29079565
PMCPMC5721783
OpenAlexW2766116738

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.