Evidence map›Paper›PMID 32293934›Full record

ReviewAmerican journal of physiology. Cell physiology2020

Epithelial transport in digestive diseases: mice, monolayers, and mechanisms.

Kim E Barrett

Open access · greenAbstract readReview
In one paragraph

Review in American journal of physiology. Cell physiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Renal Ghrelin-Family GPR39 Receptor and Urinary Concentrating Ability.Journal of the American Society of Nephrology : JASN · 2025
    Article
  5. Review
  6. Article
  7. SLC26A3 (DRA) is stimulated in a synergistic, intracellular CaAmerican journal of physiology. Cell physiology · 2023
    Article
  8. Review
  9. 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

1 author at 1 institution in 1 country.

Kim E BarrettDepartment of Medicine, University of California San Diego School of Medicine, La Jolla, California.ORCID 0000-0002-6704-998X
University of California San Diego · US

Funding

INTESTINAL SECRETORY MECHANISMS AND ANTIDIARRHEAL DRUGSR01DK028305 · NIDDK · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI BARRETT, KIM ELAINE · 1986 to 2005
$1.2M
HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) DK28305NIDDK NIH HHS R01 DK028305
6 · The paper itself

Abstract

The transport of electrolytes and fluid by the intestinal epithelium is critical in health to maintain appropriate levels of fluidity of the intestinal contents. The transport mechanisms that underlie this physiological process are also subject to derangement in various digestive disease states, such as diarrheal illnesses. This article summarizes the 2019 Hans Ussing Lecture of the Epithelial Transport Group of the American Physiological Society and discusses some pathways by which intestinal transport is dysregulated, particularly in the setting of infection with the diarrheal pathogen,

Indexed as

Intestinal AbsorptionAnimalsAntineoplastic AgentsAntiportersCell DifferentiationCell ProliferationDiarrheaEpithelial CellsErbB ReceptorsIntestinal MucosaMicePermeabilityProtein Kinase InhibitorsSalmonella Infections, AnimalSulfate TransportersAntineoplastic AgentsAntiportersEGFR protein, mouseErbB ReceptorsProtein Kinase InhibitorsSlc26a3 protein, mouseSulfate Transporterschloride secretionepidermal growth factor receptorinfectious diarrheasodium absorptionUssing chamber

Identifiers

PMID32293934
PMCPMC7311737
OpenAlexW3015451177

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.