Evidence map›Paper›PMID 30289203›Full record

ArticleAnatomical record (Hoboken, N.J. : 2007)2019

A Novel Mouse Model for Cilia-Associated Cardiovascular Anomalies with a High Penetrance of Total Anomalous Pulmonary Venous Return.

Tara A Burns, Raymond N Deepe, John Bullard, Aimee L Phelps, Katelynn A Toomer, Emilye Hiriart, Russell A Norris, Courtney J Haycraft, Andy Wessels

Abstract read
In one paragraph

Article in Anatomical record (Hoboken, N.J. : 2007), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Ciliary and Non-Ciliary Roles of IFT88 in Development and Diseases.International journal of molecular sciences · 2025
    Review
  3. Review
  4. TAPVR: Molecular Pathways and Animal Models.Advances in experimental medicine and biology · 2024
    Review
  5. Article
  6. Review
  7. Article
  8. 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

9 authors at 2 institutions in 1 country.

Tara A BurnsDepartment of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, South Carolina.
Raymond N DeepeDepartment of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, South Carolina.
John BullardDepartment of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, South Carolina.
Aimee L PhelpsDepartment of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, South Carolina.
Katelynn A ToomerDepartment of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, South Carolina.
Emilye HiriartDepartment of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, South Carolina.
Russell A NorrisDepartment of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, South Carolina.ORCID 0000-0001-8462-5726
Courtney J HaycraftDepartment of Biological Sciences, Mississippi College, Clinton, Mississippi.
Andy WesselsDepartment of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, South Carolina.ORCID 0000-0002-3805-9361
Medical University of South Carolina · USMississippi College · US

Funding

Targeted Nano-therapeutics for Neural RegenerationP20GM103444 · NIGMS · CLEMSON UNIVERSITY · PI MARKWALD, ROGER R, VYAVAHARE, NAREN R · 2012 to 2018
$14.9M
TRAINING TO IMPROVE CARDIOVASCULAR THERAPIEST32HL007260 · NHLBI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MENICK, DONALD R. · 1985 to 2021
$11.1M
Transnational Research Imaging Core (TRI)P30GM131959 · NIGMS · CLEMSON UNIVERSITY · PI VYAVAHARE, NAREN R · 2019 to 2023
$5.9M
SC COBRE for Developmentally Based Cardiovascular DiseasesP30GM103342 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI KERN, MICHAEL J · 2012 to 2016
$5.5M
MUCOPOLYSACCHRIDE METABOLISM IN CARDIAC ANOMALIESR01HL033756 · NHLBI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MARKWALD, ROGER R · 1985 to 2015
$4.8M
Cilia and Valvular Heart DiseaseR01HL131546 · NHLBI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI NORRIS, RUSSELL · 2016 to 2025
$4.4M
Mechanisms of DMP Development and Atrioventricular SeptationR01HL122906 · NHLBI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI WESSELS, ARNO · 2015 to 2025
$4.3M
Mechanisms of DMP Development and Atrioventricular SeptationR56HL122906 · NHLBI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI WESSELS, ARNO · 2014 to 2014
$374k
NHLBI NIH HHS R01 HL033756NHLBI NIH HHS R01 HL122906NHLBI NIH HHS R01 HL131546NHLBI NIH HHS R56 HL122906NHLBI NIH HHS T32 HL007260NIGMS NIH HHS P20 GM103444NIGMS NIH HHS P30 GM103342NIGMS NIH HHS P30 GM131959
6 · The paper itself

Abstract

Primary cilia are small organelles projecting from the cell surface of many cell types. They play a crucial role in the regulation of various signaling pathway. In this study, we investigated the importance of cilia for heart development by conditionally deleting intraflagellar transport protein Ift88 using the col3.6-cre mouse. Analysis of col3.6;Ift88 offspring showed a wide spectrum of cardiovascular defects including double outlet right ventricle and atrioventricular septal defects. In addition, we found that in the majority of specimens the pulmonary veins did not properly connect to the developing left atrium. The abnormal connections found resemble those seen in patients with total anomalous pulmonary venous return. Analysis of mutant hearts at early stages of development revealed abnormal development of the dorsal mesocardium, a second heart field-derived structure at the venous pole intrinsically related to the development of the pulmonary veins. Data presented support a crucial role for primary cilia in outflow tract development and atrioventricular septation and their significance for the formation of the second heart field-derived tissues at the venous pole including the dorsal mesocardium. Furthermore, the results of this study indicate that proper formation of the dorsal mesocardium is critically important for the development of the pulmonary veins. Anat Rec, 302:136-145, 2019. © 2018 Wiley Periodicals, Inc.

Indexed as

Disease Models, AnimalAnimalsCiliaCollagen Type IIIHeart Septal Defects, AtrialMaleMEF2 Transcription FactorsMiceMice, KnockoutPenetrancePulmonary VeinsScimitar SyndromeTumor Suppressor ProteinsCOL3A1 protein, mouseCollagen Type IIIMef2c protein, mouseMEF2 Transcription FactorsTg737Rpw protein, mouseTumor Suppressor Proteinsciliacongenital heart defectdevelopmentheartpulmonary veins

Identifiers

PMID30289203
PMCPMC6312498
OpenAlexW2894601702

What OpenQuestion holds

Textmetadata
LicenceTDM
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.