Evidence map›Paper›PMID 31116581›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2019

Cyclic compression increases F508 Del CFTR expression in ciliated human airway epithelium.

Nadzeya Marozkina, Jürgen Bosch, Calvin Cotton, Laura Smith, James Seckler, Khalequz Zaman, Shagufta Rehman, Ammasi Periasamy, Herbert Gaston, Ghaith Altawallbeh and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Ciliary Function, Antigen Stasis and Asthma.International journal of molecular sciences · 2024
    Review
  2. Asthma Inception: Epidemiologic Risk Factors and Natural History Across the Life Course.American journal of respiratory and critical care medicine · 2024
    Review
  3. Antigen stasis and airway nitrosative stress in human primary ciliary dyskinesia.American journal of physiology. Lung cellular and molecular physiology · 2024
    Article
  4. Article
  5. From Genetics to Precision Therapy: Finding a Path through the Scientific Valley of Death.American journal of respiratory cell and molecular biology · 2019
    Article
  6. 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

15 authors at 8 institutions in 1 country.

Nadzeya MarozkinaPediatric Pulmonology Division, Department of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, Ohio.ORCID 0000-0002-1692-8634
Jürgen BoschPediatric Pulmonology Division, Department of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, Ohio.
Calvin CottonPediatric Pulmonology Division, Department of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, Ohio.
Laura SmithPediatric Pulmonology Division, Department of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, Ohio.
James SecklerPediatric Pulmonology Division, Department of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, Ohio.
Khalequz ZamanPediatric Pulmonology Division, Department of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, Ohio.ORCID 0000-0001-9987-0388
Shagufta RehmanW. M. Keck Center for Cellular Imaging, Department of Biology, University of Virginia, Charlottesville, Virginia.
Ammasi PeriasamyW. M. Keck Center for Cellular Imaging, Department of Biology, University of Virginia, Charlottesville, Virginia.
Herbert GastonLake Effect Pharma, LLC, Gates Mills, Ohio.
Ghaith AltawallbehPediatric Pulmonology Division, Department of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, Ohio.
Michael DavisDepartment of Pediatrics, Division of Pulmonary Medicine, Children's Hospital of Richmond at Virginia Commonwealth University, Richmond, Virginia.
David R JonesThoracic Surgery Service, Memorial Sloan Kettering Cancer Center, New York, New York.
Robert SchilzPulmonology and Critical Care Medicine University Hospitals, Cleveland, Ohio.
Scott H RandellDepartment of Cell Biology and Physiology, University of North Carolina, Chapel Hill, North Carolina.
Benjamin GastonPediatric Pulmonology Division, Department of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, Ohio.
University School · USUniversity of Virginia · USGates (United States) · USMemorial Sloan Kettering Cancer Center · USRainbow Babies & Children's Hospital · USUniversity Hospitals of Cleveland · USUniversity of North Carolina at Chapel Hill · USVirginia Commonwealth University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Project 3 - Personalized cystic fibrosis treatment strategies with synergistic therapies Identified in vitro.P01HL128192 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI GASTON, BENJAMIN · 2016 to 2020
$12.2M
S-nitrosothiol signaling in pulmonary epithelial cellsP01HL101871 · NHLBI · UNIVERSITY OF VIRGINIA · PI GASTON, BENJAMIN, LEWIS, STEPHEN JOHN · 2011 to 2015
$8.7M
Epigenetic and post-translational regulation of the metastasis suppressor BRMS1R01CA136705 · NCI · UNIVERSITY OF VIRGINIA · PI JONES, DAVID R · 2009 to 2013
$1.5M
NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA136705NHLBI NIH HHS P01 HL101871NHLBI NIH HHS P01 HL128192
6 · The paper itself

Abstract

The mechanisms by which transepithelial pressure changes observed during exercise and airway clearance can benefit lung health are challenging to study. Here, we have studied 117 mature, fully ciliated airway epithelial cell filters grown at air-liquid interface grown from 10 cystic fibrosis (CF) and 19 control subjects. These were exposed to cyclic increases in apical air pressure of 15 cmH

Indexed as

Cell LineCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorEpithelial CellsEpitheliumHumansLungRespiratory MucosaCystic Fibrosis Transmembrane Conductance Regulatorairway ciliaairway clearanceairway pressurecystic fibrosis-nitrosocysteine

Identifiers

PMID31116581
PMCPMC6734384
OpenAlexW2945390780

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.