Evidence map›Paper›PMID 28775099›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2017

Alternative pre-mRNA splicing of Toll-like receptor signaling components in peripheral blood mononuclear cells from patients with ARDS.

Rachel Z Blumhagen, Brenna R Hedin, Kenneth C Malcolm, Ellen L Burnham, Marc Moss, Edward Abraham, Tristan J Huie, Jerry A Nick, Tasha E Fingerlin, Scott Alper

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

15 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Alternative splicing of toll-like receptor pathway mRNAs in lung immune cells from patients with ARDS.American journal of physiology. Lung cellular and molecular physiology · 2026
    Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Diagnostics (Basel, Switzerland) · 2021
    Article
  9. Review
  10. lncRNA NEAT1 aggravates sepsis-induced lung injury by regulating the miR-27a/PTEN axis.Laboratory investigation; a journal of technical methods and pathology · 2021
    Article
  11. Article
  12. Absence of Non-Canonical, InhibitoryFrontiers in immunology · 2021
    Article
  13. Article
  14. Article
  15. Study on Intervention Mechanism of Yiqi Huayu Jiedu Decoction on ARDS Based on Network Pharmacology.Evidence-based complementary and alternative medicine : eCAM · 2020
    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

10 authors at 3 institutions in 1 country.

Rachel Z BlumhagenCenter for Genes, Environment and Health, National Jewish Health, Denver, Colorado.
Brenna R HedinCenter for Genes, Environment and Health, National Jewish Health, Denver, Colorado.
Kenneth C MalcolmDepartment of Medicine, National Jewish Health, Denver, Colorado.
Ellen L BurnhamDivision of Pulmonary Science and Critical Care Medicine, Department of Medicine, University of Colorado Denver School of Medicine, Aurora, Colorado.
Marc MossDivision of Pulmonary Science and Critical Care Medicine, Department of Medicine, University of Colorado Denver School of Medicine, Aurora, Colorado.
Edward AbrahamOffice of the Dean, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Tristan J HuieDepartment of Medicine, National Jewish Health, Denver, Colorado.
Jerry A NickDepartment of Medicine, National Jewish Health, Denver, Colorado.
Tasha E FingerlinCenter for Genes, Environment and Health, National Jewish Health, Denver, Colorado.
Scott AlperCenter for Genes, Environment and Health, National Jewish Health, Denver, Colorado; alpers@njhealth.org.
University of Colorado Denver · USNational Jewish Health · USWake Forest University · US

Funding

Toxin-induced alternative mRNA splicing in Toll-like receptor signaling pathwaysR01ES025161 · NIEHS · NATIONAL JEWISH HEALTH · PI ALPER, SCOTT · 2016 to 2020
$1.8M
NIEHS NIH HHS R01 ES025161
6 · The paper itself

Abstract

A key physiological feature of acute respiratory distress syndrome (ARDS) is inflammation. Toll-like receptor (TLR) signaling is required to combat the infection that underlies many ARDS cases but also contributes to pathological inflammation. Several TLR signaling pathway genes encoding positive effectors of inflammation also produce alternatively spliced mRNAs encoding negative regulators of inflammation. An imbalance between these isoforms could contribute to pathological inflammation and disease severity. To determine whether splicing in TLR pathways is altered in patients with ARDS, we monitored alternative splicing of

Indexed as

Signal TransductionAlternative SplicingCytokinesHumansInflammationLeukocytes, MononuclearRespiratory Distress SyndromeRNA, MessengerRNA PrecursorsRNA SplicingToll-Like ReceptorsCytokinesRNA, MessengerRNA PrecursorsToll-Like Receptorsacute respiratory distress syndromealternative pre-mRNA splicinginflammationIRAK1MyD88peripheral blood mononuclear cell

Identifiers

PMID28775099
PMCPMC5792175
OpenAlexW2743427271

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.