Evidence map›Paper›PMID 30234375›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2018

Spontaneous pulmonary hypertension in genetic mouse models of natural killer cell deficiency.

Matthew T Rätsep, Stephen D Moore, Salema Jafri, Melissa Mitchell, Hugh J M Brady, Ofer Mandelboim, Mark Southwood, Nicholas W Morrell, Francesco Colucci, Mark L Ormiston

Open access · hybridAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Cytokine profiling in pulmonary arterial hypertension: the role of redox homeostasis and sex.Translational research : the journal of laboratory and clinical medicine · 2022
    Article
  8. Review
  9. Review
  10. A wrinkle in time: circadian biology in pulmonary vascular health and disease.American journal of physiology. Lung cellular and molecular physiology · 2022
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. The hallmarks of severe pulmonary arterial hypertension: the cancer hypothesis-ten years later.American journal of physiology. Lung cellular and molecular physiology · 2020
    Review
  16. Review
  17. Review
  18. Article
  19. 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 4 institutions in 3 countries.

Matthew T RätsepDepartments of Biomedical and Molecular Sciences, Medicine, and Surgery, Queen's University Kingston , Ontario , Canada.ORCID 0000-0001-8017-3371
Stephen D MooreDepartment of Medicine, University of Cambridge, Cambridge , United Kingdom.
Salema JafriDepartment of Medicine, University of Cambridge, Cambridge , United Kingdom.
Melissa MitchellDepartments of Biomedical and Molecular Sciences, Medicine, and Surgery, Queen's University Kingston , Ontario , Canada.
Hugh J M BradyImperial College, London, United Kingdom.
Ofer MandelboimHebrew University of Jerusalem, Jerusalem, Israel.
Mark SouthwoodDepartment of Medicine, University of Cambridge, Cambridge , United Kingdom.
Nicholas W MorrellDepartment of Medicine, University of Cambridge, Cambridge , United Kingdom.
Francesco ColucciDepartment of Obstetrics and Gynecology, University of Cambridge, Cambridge , United Kingdom.
Mark L OrmistonDepartments of Biomedical and Molecular Sciences, Medicine, and Surgery, Queen's University Kingston , Ontario , Canada.
University of Cambridge · GBQueen's University · CAHebrew University of Jerusalem · ILImperial College London · GB

Funding

British Heart Foundation FS/12/39/29653CIHR PJT-152916Wellcome Trust 200841/Z/16/Z
6 · The paper itself

Abstract

Natural killer (NK) cells are cytotoxic innate lymphoid cells with an established role in the regulation of vascular structure in pregnancy and cancer. Impaired NK cell function has been identified in patients with pulmonary arterial hypertension (PAH), a disease of obstructive vascular remodeling in the lungs, as well as in multiple rodent models of disease. However, the precise contribution of NK cell impairment to the initiation and progression of PAH remains unknown. Here, we report the development of spontaneous pulmonary hypertension in two independent genetic models of NK cell dysfunction, including Nfil3

Indexed as

AnimalsBasic-Leucine Zipper Transcription FactorsDisease Models, AnimalEndothelial CellsHumansHypertension, PulmonaryKiller Cells, NaturalLungMiceNatural Cytotoxicity Triggering Receptor 1Pulmonary ArteryVascular RemodelingBasic-Leucine Zipper Transcription FactorsNatural Cytotoxicity Triggering Receptor 1angiopoietin-2interleukin-23natural killer cellspulmonary hypertensionTh17

Identifiers

PMID30234375
PMCPMC6337009
OpenAlexW2890958810

What OpenQuestion holds

Textmetadata
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.