Evidence map›Paper›PMID 12409607›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2002

Molecular characterization of mouse gastric epithelial progenitor cells.

Jason C Mills, Niklas Andersson, Chieu V Hong, Thaddeus S Stappenbeck, Jeffrey I Gordon

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

32 citing papers in PubMed, 96 citations in OpenAlex.

  1. Trial
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  4. The EJC component Magoh in non-vertebrate chordates.Development genes and evolution · 2020
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  5. Review
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  11. Gastric epithelial stem cells.Gastroenterology · 2011
    Review
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  15. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Jason C MillsDepartment of Molecular Biology and Pharmacology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Niklas Andersson
Chieu V Hong
Thaddeus S Stappenbeck
Jeffrey I Gordon
Washington University in St. Louis · US

Funding

GNOTOBIOTIC TRANSGENIC MODELS OF THE GASTRIC ECOSYSTEMR01DK058529 · NIDDK · WASHINGTON UNIVERSITY · PI GORDON, JEFFREY I · 2001 to 2010
$3.5M
NIDDK NIH HHS DK58529NIDDK NIH HHS R01 DK058529
6 · The paper itself

Abstract

The adult mouse gastric epithelium undergoes continuous renewal in discrete anatomic units. Lineage tracing studies have previously disclosed the morphologic features of gastric epithelial lineage progenitors (GEPs), including those of the presumptive multipotent stem cell. However, their molecular features have not been defined. Here, we present the results of an analysis of genes and pathways expressed in these cells. One hundred forty-seven transcripts enriched in GEPs were identified using an approach that did not require physical disruption of the stem cell niche. Real-time quantitative RT-PCR studies of laser capture microdissected cells retrieved from this niche confirmed enriched expression of a selected set of genes from the GEP list. An algorithm that allows quantitative comparisons of the functional relatedness of automatically annotated expression profiles showed that the GEP profile is similar to a dataset of genes that defines mouse hematopoietic stem cells, and distinct from the profiles of two differentiated GEP descendant lineages (parietal and zymogenic cell). Overall, our analysis revealed that growth factor response pathways are prominent in GEPs, with insulin-like growth factor appearing to play a key role. A substantial fraction of GEP transcripts encode products required for mRNA processing and cytoplasmic localization, including numerous homologs of Drosophila genes (e.g., Y14, staufen, mago nashi) needed for axis formation during oogenesis. mRNA targeting proteins may help these epithelial progenitors establish differential communications with neighboring cells in their niche.

Indexed as

Adenosine TriphosphateAnimalsCell NucleusCytoplasmDiphtheria ToxinGastric MucosaGlycolysisMiceMice, TransgenicParietal Cells, GastricPeptide FragmentsReverse Transcriptase Polymerase Chain ReactionStem CellsStomachTranscription, GeneticAdenosine TriphosphateDiphtheria Toxindiphtheria toxin fragment APeptide Fragments

Identifiers

PMID12409607
PMCPMC137502
OpenAlexW2009343546

What OpenQuestion 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 OpenQuestion graph.