Evidence map›Paper›PMID 19897012›Full record

ReviewMolecular and cellular endocrinology2010

Reprogramming into pancreatic endocrine cells based on developmental cues.

Simon Kordowich, Ahmed Mansouri, Patrick Collombat

Abstract readReview
In one paragraph

Review in Molecular and cellular endocrinology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. GABA signalling in human pancreatic islets.Frontiers in endocrinology · 2023
    Review
  2. GABAInternational journal of molecular sciences · 2020
    Article
  3. Review
  4. Article
  5. Emerging roles for the TGFbeta family in pancreatic beta-cell homeostasis.Trends in endocrinology and metabolism: TEM · 2010
    Article
  6. 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

3 authors.

Simon KordowichMax-Planck Institute for Biophysical Chemistry, Department of Molecular Cell Biology, Am Fassberg, D-37077 Göttingen, Germany.
Ahmed Mansouri
Patrick Collombat

Funding

Pancreatic endocrine development and regenerationU19DK072495 · NIDDK · HAGEDORN RESEARCH INSTITUTE · PI SERUP, PALLE · 2005 to 2009
$5.6M
NIDDK NIH HHS U19 DK072495NIDDK NIH HHS U19 DK 072495-01
6 · The paper itself

Abstract

Due to the increasing prevalence of type 1 diabetes and the complications arising from actual therapies, alternative treatments need to be established. In order to compensate the beta-cell deficiency associated with type 1 diabetes, current research focuses on new strategies to generate insulin-producing beta-cells for transplantation purpose, including the differentiation of stem or progenitor cells, as well as the transdifferentiation of dispensable mature cell types. However, to successfully force specific cells to adopt a functional beta-cell fate or phenotype, a better understanding of the molecular mechanisms underlying beta-cell genesis is required. The present short review summarizes the hitherto known functions and interplays of several key factors involved in the development of the different endocrine cell lineages during pancreas morphogenesis, as well as their potential to direct the generation of beta-cells. Furthermore, an emphasis is made on beta-cell regeneration and the determinants implicated.

Indexed as

Insulin-Secreting CellsPancreasAnimalsCell DifferentiationCell LineageDiabetes Mellitus, Type 1Embryo, MammalianHumansMorphogenesisRegenerationStem Cells

Identifiers

PMID19897012
PMCPMC2814956

What OpenQuestion holds

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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.