Evidence map›Paper›PMID 26417411›Full record

ArticleJournal of diabetes investigation2015

Establishment of maturity-onset diabetes of the young-induced pluripotent stem cells from a Japanese patient.

Shigeharu G Yabe, Naoko Iwasaki, Kazuki Yasuda, Tatsuo S Hamazaki, Masamitsu Konno, Satsuki Fukuda, Fujie Takeda, Masato Kasuga, Hitoshi Okochi

Open access · goldAbstract read
In one paragraph

Article in Journal of diabetes investigation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Modelling human diabetesFrontiers in endocrinology · 2024
    Review
  4. Review
  5. Article
  6. Review
  7. Modeling different types of diabetes using human pluripotent stem cells.Cellular and molecular life sciences : CMLS · 2021
    Review
  8. Article
  9. Recent progress in pancreatic islet cell therapy.Inflammation and regeneration · 2021
    Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. iPSC technology-based regenerative therapy for diabetes.Journal of diabetes investigation · 2018
    Review
  17. Beta-cell replacement strategies for diabetes.Journal of diabetes investigation · 2017
    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

9 authors at 2 institutions in 1 country.

Shigeharu G YabeDepartment of Regenerative Medicine, Research Institute, National Center for Global Health and Medicine Tokyo, Japan.
Naoko IwasakiDiabetes Center, Tokyo Women's Medical University Tokyo, Japan.
Kazuki YasudaDepartment of Metabolic Disorders, Diabetes Research Center, National Center for Global Health and Medicine Tokyo, Japan.
Tatsuo S HamazakiDepartment of Regenerative Medicine, Research Institute, National Center for Global Health and Medicine Tokyo, Japan.
Masamitsu KonnoDepartment of Regenerative Medicine, Research Institute, National Center for Global Health and Medicine Tokyo, Japan.
Satsuki FukudaDepartment of Regenerative Medicine, Research Institute, National Center for Global Health and Medicine Tokyo, Japan.
Fujie TakedaDepartment of Regenerative Medicine, Research Institute, National Center for Global Health and Medicine Tokyo, Japan.
Masato KasugaNational Center for Global Health and Medicine Tokyo, Japan.
Hitoshi OkochiDepartment of Regenerative Medicine, Research Institute, National Center for Global Health and Medicine Tokyo, Japan.
National Center for Global Health and Medicine · JPTokyo Women's Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Maturity-onset diabetes of the young (MODY) is a heterozygous monogenic diabetes; more than 13 disease genes have been identified. However, the pathogenesis of MODY is not fully understood, because the pancreatic β-cells of the patients are inaccessable. Therefore, we attempted to establish MODY patient-derived induced pluripotent stem cells (MODY-iPS) cells to investigate the pathogenic mechanism of MODY by inducing pancreatic β-cells. We established MODY5-iPS cells from a Japanese patient with MODY5 (R177X), and confirmed that MODY5-iPS cells possessed the characteristics of pluripotent stem cells. In the course of differentiation from MODY5-iPS cells into pancreatic β-cells, we examined the disease gene, HNF1B messenger ribonucleic acid. We found that the amount of R177X mutant transcripts was much less than that of wild ones, but they increased after adding cycloheximide to the medium. These results suggest that these R177X mutant messenger ribonucleic acids are disrupted by nonsense-mediated messenger ribonucleic acid decay in MODY-iPS cells during the developmental stages of pancreatic β-cells.

Indexed as

DiabetesMaturity-onset diabetes of the youngPluripotent stem cells

Identifiers

PMID26417411
PMCPMC4578493
OpenAlexW2079144867

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.