Evidence map›Paper›PMID 38650964›Full record

ArticleSymmetry2023

Striped Expression of Leucine-Rich Repeat Proteins Coordinates Cell Intercalation and Compartment Boundary Formation in the Early

Chloe A Kuebler, Adam C Paré

Open access · goldAbstract read
In one paragraph

Article in Symmetry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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 1 institution in 1 country.

Chloe A KueblerDepartment of Biological Sciences, University of Arkansas, Fayetteville, AR 72701, USA.ORCID 0009-0008-7842-8345
Adam C ParéDepartment of Biological Sciences, University of Arkansas, Fayetteville, AR 72701, USA.
University of Arkansas at Fayetteville · US

Funding

Unraveling Gene-Environment Interactions Shaping Metabolism: A Multi-Omics Analysis in DrosophilaP20GM139768 · NIGMS · UNIVERSITY OF ARKANSAS AT FAYETTEVILLE · PI Joanna Fiddler · 2021 to 2026
$17.0M
Control of epithelial morphology and bioenergetics by Toll receptors during dynamic tissue remodelingR01GM147372 · NIGMS · UNIVERSITY OF ARKANSAS AT FAYETTEVILLE · PI Adam Christopher Pare · 2023 to 2026
$1.2M
Defining the molecular and cellular bases of tissue compartmentalizationR15GM143729 · NIGMS · UNIVERSITY OF ARKANSAS AT FAYETTEVILLE · PI PARE, ADAM CHRISTOPHER · 2021 to 2021
$437k
NIGMS NIH HHS P20 GM139768NIGMS NIH HHS R01 GM147372NIGMS NIH HHS R15 GM143729
6 · The paper itself

Abstract

Planar polarity is a commonly observed phenomenon in which proteins display a consistent asymmetry in their subcellular localization or activity across the plane of a tissue. During animal development, planar polarity is a fundamental mechanism for coordinating the behaviors of groups of cells to achieve anisotropic tissue remodeling, growth, and organization. Therefore, a primary focus of developmental biology research has been to understand the molecular mechanisms underlying planar polarity in a variety of systems to identify conserved principles of tissue organization. In the early

Indexed as

cell intercalationCirlcompartment boundaryconvergent extensionleucine-rich repeatplanar polarityTartanTen-mToll receptors

Identifiers

PMID38650964
PMCPMC11034934
OpenAlexW4385344881

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.