Evidence map›Paper›PMID 31959287›Full record

ReviewCurrent topics in developmental biology2020

Cellular, molecular, and biophysical control of epithelial cell intercalation.

Adam C Paré, Jennifer A Zallen

Open access · greenAbstract readReview
In one paragraph

Review in Current topics in developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
16.4field-weighted citation impact, top 1% 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

36 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
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  4. bioRxiv : the preprint server for biology · 2026
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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

2 authors at 2 institutions in 1 country.

Adam C ParéDepartment of Biological Sciences, University of Arkansas, Fayetteville, AR, United States. Electronic address: pare@uark.edu.
Jennifer A ZallenHoward Hughes Medical Institute and Developmental Biology Program, Sloan Kettering Institute, New York, NY, United States. Electronic address: zallenj@mskcc.org.
Howard Hughes Medical Institute · USUniversity of Arkansas at Fayetteville · US

Funding

Molecular control of tissue morphogenesisR01GM079340 · NIGMS · SLOAN-KETTERING INST CAN RESEARCH · PI ZALLEN, JENNIFER A · 2007 to 2021
$4.2M
Howard Hughes Medical InstituteNIGMS NIH HHS R01 GM079340
6 · The paper itself

Abstract

Convergent extension is a conserved mechanism for elongating tissues. In the Drosophila embryo, convergent extension is driven by planar polarized cell intercalation and is a paradigm for understanding the cellular, molecular, and biophysical mechanisms that establish tissue structure. Studies of convergent extension in Drosophila have provided key insights into the force-generating molecules that promote convergent extension in epithelial tissues, as well as the global systems of spatial information that systematically organize these cell behaviors. A general framework has emerged in which asymmetrically localized proteins involved in cytoskeletal tension and cell adhesion direct oriented cell movements, and spatial signals provided by the Toll, Tartan, and Teneurin receptor families break planar symmetry to establish and coordinate planar cell polarity throughout the tissue. In this chapter, we describe the cellular, molecular, and biophysical mechanisms that regulate cell intercalation in the Drosophila embryo, and discuss how research in this system has revealed conserved biological principles that control the organization of multicellular tissues and animal body plans.

Indexed as

Cell CommunicationMorphogenesisAnimalsCell AdhesionCell MovementCell PolarityCytoskeletonDrosophila melanogasterDrosophila ProteinsEmbryo, NonmammalianEpithelial CellsGene Expression Regulation, DevelopmentalSignal TransductionDrosophila ProteinsBiomechanicsCell intercalationCompartment boundaryConvergent extensionDrosophilaGermband extensionMyosinPlanar polarityTeneurinToll receptors

Identifiers

PMID31959287
PMCPMC8559432
OpenAlexW3000216180

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.