Evidence map›Paper›PMID 32592286›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2020

37/67-laminin receptor facilitates neural crest cell migration during enteric nervous system development.

Ming Fu, Amanda J Barlow-Anacker, Korah P Kuruvilla, Gary L Bowlin, Christopher W Seidel, Paul A Trainor, Ankush Gosain

Open access · bronzeAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. The Impact of MutantAnimals : an open access journal from MDPI · 2025
    Article
  9. Article
  10. Article
  11. Endothelin signaling in development.Development (Cambridge, England) · 2023
    Review
  12. Hirschsprung disease.Nature reviews. Disease primers · 2023
    Review
  13. Review
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

7 authors at 5 institutions in 1 country.

Ming FuDivision of Pediatric Surgery, Department of Surgery, University of Tennessee Health Sciences Center, Memphis, TN, USA.
Amanda J Barlow-AnackerDepartment of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Korah P KuruvillaDivision of Pediatric Surgery, Department of Surgery, University of Tennessee Health Sciences Center, Memphis, TN, USA.
Gary L BowlinDepartment of Biomedical Engineering, University of Memphis, Memphis, TN, USA.
Christopher W SeidelStowers Institute for Medical Research, Kansas City, MO, USA.
Paul A TrainorStowers Institute for Medical Research, Kansas City, MO, USA.
Ankush GosainDivision of Pediatric Surgery, Department of Surgery, University of Tennessee Health Sciences Center, Memphis, TN, USA.
Stowers Institute for Medical Research · USUniversity of Tennessee Health Science Center · USLe Bonheur Children's Hospital · USUniversity of Memphis · USUniversity of Wisconsin–Madison · US

Funding

Dysbiosis in Hirschsprung Associated Enterocolitis PathogenesisR01DK125047 · NIDDK · UNIVERSITY OF VIRGINIA · PI GOSAIN, ANKUSH · 2020 to 2024
$2.1M
Gastrointestinal Mucosal Immune Defects in Hirschsprungs DiseaseK08DK098271 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI GOSAIN, ANKUSH · 2014 to 2018
$815k
Validating Intestinal Enteroids to Study Hirschsprung's Associated EnterocolitisR03DK114543 · NIDDK · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI GOSAIN, ANKUSH · 2017 to 2018
$152k
NIDDK NIH HHS K08 DK098271NIDDK NIH HHS R01 DK125047NIDDK NIH HHS R03 DK114543
6 · The paper itself

Abstract

Enteric nervous system (ENS) development is governed by interactions between neural crest cells (NCC) and the extracellular matrix (ECM). Hirschsprung disease (HSCR) results from incomplete NCC migration and failure to form an appropriate ENS. Prior studies implicate abnormal ECM in NCC migration failure. We performed a comparative microarray of the embryonic distal hindgut of wild-type and EdnrB

Indexed as

AnimalsCell MovementColonDown-RegulationEnteric Nervous SystemHirschsprung DiseaseHumansLamininMiceMice, KnockoutNeural CrestOrganogenesisReceptor, Endothelin BReceptors, LamininUp-RegulationLamininReceptor, Endothelin BReceptors, Laminindevelopmentextracellular matrixHirschsprung diseaseneural crest

Identifiers

PMID32592286
PMCPMC7759089
OpenAlexW3037058066

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.