Evidence map›Paper›PMID 40042272›Full record

ArticlemBio2025

Spontaneous lung colonization in the cystic fibrosis rat model is linked to gastrointestinal obstruction.

Mikayla Murphree-Terry, Johnathan D Keith, Ashley M Oden, Susan E Birket

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in mBio, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Considerations for early life genetic therapies in cystic fibrosis.American journal of physiology. Lung cellular and molecular physiology · 2026
    Review
  2. 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

4 authors.

Mikayla Murphree-TerryDepartment of Medicine, Division of Pulmonary, Allergy, and Critical Care Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.ORCID 0000-0001-7390-9512
Johnathan D KeithGregory Fleming James Cystic Fibrosis Research Center, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Ashley M OdenDepartment of Medicine, Division of Pulmonary, Allergy, and Critical Care Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Susan E BirketDepartment of Medicine, Division of Pulmonary, Allergy, and Critical Care Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.ORCID 0000-0002-6353-6596

Funding

UAB CF Research and Translation Core CenterP30DK072482 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI AMIT GAGGAR · 2007 to 2026
$23.0M
The Role of Airway Mucus in Infection and InflammationR01HL153079 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BIRKET, SUSAN ELIZABETH · 2021 to 2025
$2.2M
Cystic Fibrosis Foundation (CFF) ROWE19R0HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01HL153079NHLBI NIH HHS R01 HL153079NIDDK NIH HHS P30 DK072482
6 · The paper itself

Abstract

Cystic fibrosis (CF) is a genetic disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (

Indexed as

Cystic FibrosisIntestinal ObstructionLungPseudomonas InfectionsAminophenolsAnimalsCystic Fibrosis Transmembrane Conductance RegulatorDisease Models, AnimalFecesGastrointestinal MicrobiomeHumansMalePseudomonas aeruginosaQuinolonesRatsAminophenolsCystic Fibrosis Transmembrane Conductance RegulatorivacaftorQuinolonesairway colonizationcystic fibrosisDIOSmicrobiomemucus

Identifiers

PMID40042272
PMCPMC11980572

What OpenQuestion holds

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LicenceCC BY
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.