Evidence map›Paper›PMID 16107537›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2005

Direct regulation of intestinal fate by Notch.

Ben Z Stanger, Radhika Datar, L Charles Murtaugh, Douglas A Melton

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00954252 (Placebo-Controlled, Ascending Single-Dose Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of CHF 5074 in Healthy Young Male Subjects), which is not on this map. Cited by 165 papers.

0numbers the graph read from it
0cells of the map it votes in
165citing papers in PubMed
5.5field-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.

NCT00954252 phase1completednot on this mapstarted 2009, after this paper: background citation

Placebo-Controlled, Ascending Single-Dose Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of CHF 5074 in Healthy Young Male Subjects

TypeinterventionalSponsorCERESPIRRan2009 to 2010Enrolled84ConditionsAlzheimer's DiseaseArmsCHF 5074, placebo
3 · Its place in the literature

Who cites it

165 citing papers in PubMed, 294 citations in OpenAlex.

  1. Developmental regulation of intestinalbioRxiv : the preprint server for biology · 2025
    Article
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  3. Nuclei sense complex tissue shape and direct intestinal stem cell fate.bioRxiv : the preprint server for biology · 2025
    Article
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  13. The emerging roles of deep crypt secretory cells in colonic physiology.American journal of physiology. Gastrointestinal and liver physiology · 2023
    Review
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  15. Review
  16. Article
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  19. Review
  20. Review

105 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 2 countries.

Ben Z StangerHoward Hughes Medical Institute and Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.
Radhika Datar
L Charles Murtaugh
Douglas A Melton
Harvard University · USHoward Hughes Medical Institute · US

Funding

Molecular Regulation of Pancreas Cell Fate DeterminationK08DK064136 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI STANGER, BEN Z · 2003 to 2007
$649k
NIDDK NIH HHS K08 DK064136
6 · The paper itself

Abstract

The signals that maintain the proper balance between adult intestinal cell types are poorly understood. Loss-of-function studies have implicated the Notch pathway in the regulation of intestinal fate during development. However, it is unknown whether Notch has a role in maintaining the balance of different cell types in the adult intestine and whether it acts reversibly. To determine whether Notch has a direct effect on intestinal development and adult intestinal cell turnover, we have used a gain-of-function approach to activate Notch. Ectopic Notch signaling in adult intestinal progenitor cells leads to a bias against secretory fates, whereas ectopic Notch activation in the embryonic foregut results in reversible defects in villus morphogenesis and loss of the proliferative progenitor compartment. We conclude that Notch regulates adult intestinal development by controlling the balance between secretory and absorptive cell types. In the embryo, Notch activation perturbs morphogenesis, possibly through effects on stem or progenitor cells.

Indexed as

AnimalsCell DifferentiationFemaleGene Expression Regulation, DevelopmentalIntestinal MucosaIntestinesMaleMiceMice, Inbred ICRMice, TransgenicPregnancyReceptor, Notch1Receptors, Cell SurfaceSignal TransductionStem CellsTranscription FactorsNotch1 protein, mouseReceptor, Notch1Receptors, Cell SurfaceTranscription Factors

Identifiers

PMID16107537
PMCPMC1194941
OpenAlexW1990442683

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.