Evidence map›Paper›PMID 24831984›Full record

ReviewTrends in endocrinology and metabolism: TEM2014

Revealing transcription factors during human pancreatic β cell development.

Elizabeth Conrad, Roland Stein, Chad S Hunter

Open access · greenAbstract readReview
In one paragraph

Review in Trends in endocrinology and metabolism: TEM, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

40 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
  2. Article
  3. mThe EMBO journal · 2024
    Article
  4. Article
  5. Review
  6. An Insight into Vital Genes Responsible for β-cell Formation.Advances in experimental medicine and biology · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. A distinct role of STING in regulating glucose homeostasis through insulin sensitivity and insulin secretion.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  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

3 authors at 1 institution in 1 country.

Elizabeth ConradDepartment of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, 2215 Garland Ave, Nashville, TN 37232, USA.
Roland SteinDepartment of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, 2215 Garland Ave, Nashville, TN 37232, USA.
Chad S HunterDepartment of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, 2215 Garland Ave, Nashville, TN 37232, USA. Electronic address: huntercs@uab.edu.
Vanderbilt University Medical Center · US

Funding

Molecular Mechanisms of Human and Murine Beta Cell Proliferation and RegenerationU01DK089572 · NIDDK · VANDERBILT UNIVERSITY · PI GREINER, DALE LESLIE, HARLAN, DAVID MARSHALL · 2010 to 2014
$8.4M
TRAINING PROGRAM IN CELLULAR, BIOCHEMICAL, &MOLECULAR ST32GM008554 · NIGMS · VANDERBILT UNIVERSITY · PI PATTON, JAMES G. · 1995 to 2020
$7.4M
PDX-1,A TRANSCRIPTIONAL ACTIVATOR OF THE INSULIN GENER01DK050203 · NIDDK · VANDERBILT UNIVERSITY · PI BASS, JOSEPH, STEIN, ROLAND W · 1995 to 2020
$6.8M
Defining the Role of MafA in Islet Beta CellsR01DK090570 · NIDDK · VANDERBILT UNIVERSITY · PI PARENT, AUDREY, STEIN, ROLAND W · 2011 to 2025
$5.9M
The Ldb1 coregulator controls LIM target genes in developing and adult islets.K01DK094842 · NIDDK · VANDERBILT UNIVERSITY · PI HUNTER, CHAD S · 2013 to 2015
$404k
Control of islet b-specific pdx-1 &mafA transcriptionR56DK050203 · NIDDK · VANDERBILT UNIVERSITY · PI STEIN, ROLAND W · 2005 to 2005
$76k
NIDDK NIH HHS DK050203NIDDK NIH HHS DK089572NIDDK NIH HHS DK090570NIDDK NIH HHS DK094842NIDDK NIH HHS K01 DK094842NIDDK NIH HHS R01 DK050203NIDDK NIH HHS R01 DK090570NIDDK NIH HHS R56 DK050203NIDDK NIH HHS U01 DK089572NIGMS NIH HHS T32 GM008554NIGMS NIH HHS T32GM008554
6 · The paper itself

Abstract

Developing cell-based diabetes therapies requires examining transcriptional mechanisms underlying human β cell development. However, increased knowledge is hampered by low availability of fetal pancreatic tissue and gene targeting strategies. Rodent models have elucidated transcription factor roles during islet organogenesis and maturation, but differences between mouse and human islets have been identified. The past 5 years have seen strides toward generating human β cell lines, the examination of human transcription factor expression, and studies utilizing induced pluripotent stem cells (iPS cells) and human embryonic stem (hES) cells to generate β-like cells. Nevertheless, much remains to be resolved. We present current knowledge of developing human β cell transcription factor expression, as compared to rodents. We also discuss recent studies employing transcription factor or epigenetic modulation to generate β cells.

Indexed as

HumansInsulin-Secreting CellsIslets of LangerhansOrganogenesisTranscription FactorsTranscription Factorsdiabetes mellitusepigeneticshumanorganogenesistranscription factor

Identifiers

PMID24831984
PMCPMC4167784
OpenAlexW2033906871

What OpenQuestion holds

Textmetadata
LicenceTDM
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.