Evidence map›Paper›PMID 30551650›Full record

ReviewNon-coding RNA2018

Non-Coding RNA in Pancreas and β-Cell Development.

Wilson K M Wong, Anja E Sørensen, Mugdha V Joglekar, Anand A Hardikar, Louise T Dalgaard

Open access · goldAbstract readReview
In one paragraph

Review in Non-coding RNA, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
5.9field-weighted citation impact, top 3% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Micro-RNA Implications in Type-1 Diabetes Mellitus: A Review of Literature.International journal of molecular sciences · 2021
    Review
  17. Review
  18. Observational
  19. Article
  20. 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

5 authors at 2 institutions in 2 countries.

Wilson K M WongNHMRC Clinical Trials Center, University of Sydney, Camperdown NSW 2050, Sydney, Australia. wilson.wong@ctc.usyd.edu.au.
Anja E SørensenDepartment of Science and Environment, Roskilde University, DK-4000 Roskilde, Denmark. elaine@ruc.dk.
Mugdha V JoglekarNHMRC Clinical Trials Center, University of Sydney, Camperdown NSW 2050, Sydney, Australia. mugdha.joglekar@ctc.usyd.edu.au.
Anand A HardikarNHMRC Clinical Trials Center, University of Sydney, Camperdown NSW 2050, Sydney, Australia. anand.hardikar@ctc.usyd.edu.au.
Louise T DalgaardDepartment of Science and Environment, Roskilde University, DK-4000 Roskilde, Denmark. ltd@ruc.dk.ORCID 0000-0002-3598-2775
The University of Sydney · AURoskilde University · DK

Funding

Danish Diabetes Academy PhD fellowshipJuvenile Diabetes Research Foundation Australia T1D Clinical Research NetworkJuvenile Diabetes Research Foundation United States of America Advanced Post-doctoral award
6 · The paper itself

Abstract

In this review, we provide an overview of the current knowledge on the role of different classes of non-coding RNAs for islet and β-cell development, maturation and function. MicroRNAs (miRNAs), a prominent class of small RNAs, have been investigated for more than two decades and patterns of the roles of different miRNAs in pancreatic fetal development, islet and β-cell maturation and function are now emerging. Specific miRNAs are dynamically regulated throughout the period of pancreas development, during islet and β-cell differentiation as well as in the perinatal period, where a burst of β-cell replication takes place. The role of long non-coding RNAs (lncRNA) in islet and β-cells is less investigated than for miRNAs, but knowledge is increasing rapidly. The advent of ultra-deep RNA sequencing has enabled the identification of highly islet- or β-cell-selective lncRNA transcripts expressed at low levels. Their roles in islet cells are currently only characterized for a few of these lncRNAs, and these are often associated with β-cell super-enhancers and regulate neighboring gene activity. Moreover, ncRNAs present in imprinted regions are involved in pancreas development and β-cell function. Altogether, these observations support significant and important actions of ncRNAs in β-cell development and function.

Indexed as

circular RNAsfetal developmentislets of Langerhanslong intergenic non-coding RNAslong non-coding RNAsmicroRNAnon-coding RNAspancreaspiwi associated RNAssmall nucleolar RNAsα-cellβ-cell

Identifiers

PMID30551650
PMCPMC6315983
OpenAlexW2903864161

What OpenQuestion 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 OpenQuestion graph.