Evidence map›Paper›PMID 29113996›Full record

ArticleMolecular & cellular proteomics : MCP2018

Characterization of the Molecular Mechanisms Underlying Glucose Stimulated Insulin Secretion from Isolated Pancreatic β-cells Using Post-translational Modification Specific Proteomics (PTMomics).

Taewook Kang, Pia Jensen, Honggang Huang, Gitte Lund Christensen, Nils Billestrup, Martin R Larsen

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Pancreatic β-cell heterogeneity in health and diabetes: classes, sources, and subtypes.American journal of physiology. Endocrinology and metabolism · 2021
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. The Role of Semaphorins in Metabolic Disorders.International journal of molecular sciences · 2020
    Review
  15. Article
  16. Article
  17. β-Cell Maturation and Identity in Health and Disease.International journal of molecular sciences · 2019
    Review
  18. Article
  19. Review
  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

6 authors at 2 institutions in 1 country.

Taewook KangFrom the ‡Department of Biochemistry and Molecular Biology, PR group, University of Southern Denmark, Odense, Denmark.
Pia JensenFrom the ‡Department of Biochemistry and Molecular Biology, PR group, University of Southern Denmark, Odense, Denmark.
Honggang HuangFrom the ‡Department of Biochemistry and Molecular Biology, PR group, University of Southern Denmark, Odense, Denmark.
Gitte Lund Christensen§Department of Biomedical Sciences, University of Copenhagen, 2200 Copenhagen N, Denmark.
Nils Billestrup§Department of Biomedical Sciences, University of Copenhagen, 2200 Copenhagen N, Denmark.
Martin R LarsenFrom the ‡Department of Biochemistry and Molecular Biology, PR group, University of Southern Denmark, Odense, Denmark; mrl@bmb.sdu.dk.
University of Southern Denmark · DKUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Normal pancreatic islet β-cells (PBCs) abundantly secrete insulin in response to elevated blood glucose levels, in order to maintain an adequate control of energy balance and glucose homeostasis. However, the molecular mechanisms underlying the insulin secretion are unclear. Improving our understanding of glucose-stimulated insulin secretion (GSIS) mechanisms under normal conditions is a prerequisite for developing better interventions against diabetes. Here, we aimed at identifying novel signaling pathways involved in the initial release of insulin from PBCs after glucose stimulation using quantitative strategies for the assessment of phosphorylated proteins and sialylated

Indexed as

AnimalsAnimals, NewbornGlucoseInsulin-Secreting CellsInsulin SecretionProtein Processing, Post-TranslationalProteomicsRats, WistarSignal TransductionGlucose

Identifiers

PMID29113996
PMCPMC5750853
OpenAlexW2767407162

What Socratic holds

Textmetadata
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.