Evidence map›Paper›PMID 35813631›Full record

ReviewFrontiers in endocrinology2022

Cilia Action in Islets: Lessons From Mouse Models.

Jung Hoon Cho, Jing W Hughes

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Islet cilia and glucose homeostasis.Frontiers in cell and developmental biology · 2022
    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

2 authors at 1 institution in 1 country.

Jung Hoon ChoDepartment of Medicine, Washington University School of Medicine, Saint Louis, MO, United States.
Jing W HughesDepartment of Medicine, Washington University School of Medicine, Saint Louis, MO, United States.
Washington University in St. Louis · US

Funding

GLUCAGON REGULATION BY A NOVEL BROWN ADIPOSE FACTORK08DK115795 · NIDDK · WASHINGTON UNIVERSITY · PI HUGHES, JING WANG · 2018 to 2022
$768k
Primary Cilia in Human T1D PancreasR03DK127748 · NIDDK · WASHINGTON UNIVERSITY · PI HUGHES, JING WANG · 2020 to 2021
$315k
NIDDK NIH HHS K08 DK115795NIDDK NIH HHS R03 DK127748
6 · The paper itself

Abstract

Primary cilia as a signaling organelle have garnered recent attention as a regulator of pancreatic islet function. These rod-like sensors exist on all major islet endocrine cell types and transduce a variety of external cues, while dysregulation of cilia function contributes to the development of diabetes. The complex role of islet primary cilia has been examined using genetic deletion targeting various components of cilia. In this review, we summarize experimental models for the study of islet cilia and current understanding of mechanisms of cilia regulation of islet hormone secretion. Consensus from these studies shows that pancreatic cilia perturbation can cause both endocrine and exocrine defects that are relevant to human disease. We discuss future research directions that would further elucidate cilia action in distinct groups of islet cells, including paracrine and juxtacrine regulation, GPCR signaling, and endocrine-exocrine crosstalk.

Indexed as

Diabetes MellitusInsulin-Secreting CellsIslets of LangerhansAnimalsCiliaDisease Models, AnimalMicePancreashormone regulationinsulin secretionpancreatic isletsprimary ciliaβ-cells

Identifiers

PMID35813631
PMCPMC9260721
OpenAlexW4283324733

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.