Evidence map›Paper›PMID 19750517›Full record

ReviewBirth defects research. Part C, Embryo today : reviews2009

Pancreas cell fate.

Michelle A Guney, Maureen Gannon

Abstract readReview
In one paragraph

Review in Birth defects research. Part C, Embryo today : reviews, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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

38 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Human embryonic stem cells as anWorld journal of stem cells · 2020
    Review
  13. Review
  14. Pancreatic β cell regeneration: To β or not to β.Current opinion in physiology · 2020
    Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Mesenchymal stem cell therapy in type 2 diabetes mellitus.Diabetology & metabolic syndrome · 2017
    Review
  20. 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.

Michelle A GuneyDepartment of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Maureen Gannon

Funding

HNF6 Function in the Pancreatic Endocrine LineageR01DK065131 · NIDDK · VANDERBILT UNIVERSITY · PI GANNON, MAUREEN A · 2003 to 2010
$1.7M
Foxm 1b endocrine pancreas growth and regenerationR01DK071052 · NIDDK · VANDERBILT UNIVERSITY · PI GANNON, MAUREEN A · 2006 to 2009
$1.0M
Foxm 1b in Endocrine Pancreas Growth and RegenerationR56DK071052 · NIDDK · VANDERBILT UNIVERSITY · PI GANNON, MAUREEN A · 2005 to 2010
$346k
NIDDK NIH HHS DK065131NIDDK NIH HHS DK071052NIDDK NIH HHS DK07563NIDDK NIH HHS R01 DK065131NIDDK NIH HHS R01 DK071052NIDDK NIH HHS R56 DK071052
6 · The paper itself

Abstract

Diabetes is characterized by decreased function of insulin-producing beta cells and insufficient insulin output resulting from an absolute (Type 1) or relative (Type 2) inadequate functional beta cell mass. Both forms of the disease would greatly benefit from treatment strategies that could enhance beta cell regeneration and/or function. Successful and reliable methods of generating beta cells or whole islets from progenitor cells in vivo or in vitro could lead to restoration of beta cell mass in individuals with Type 1 diabetes and enhanced beta cell compensation in Type 2 patients. A thorough understanding of the normal developmental processes that occur during pancreatic organogenesis, for example, transcription factors, cell signaling molecules, and cell-cell interactions that regulate endocrine differentiation from the embryonic pancreatic epithelium, is required in order to successfully reach these goals. This review summarizes our current understanding of pancreas development, with particular emphasis on factors intrinsic or extrinsic to the pancreatic epithelium that are involved in regulating the development and differentiation of the various pancreatic cell types. We also discuss the recent progress in generating insulin-producing cells from progenitor sources.

Indexed as

Cell DifferentiationGene Expression Regulation, DevelopmentalSignal TransductionAnimalsCell LineageEmbryo, MammalianHumansPancreasTranscription FactorsTranscription Factors

Identifiers

PMID19750517
PMCPMC2755625

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.