Evidence map›Paper›PMID 30541790›Full record

ArticleScience translational medicine2018

Comment on "ALK is a therapeutic target for lethal sepsis".

Rafael B Blasco, Enrico Patrucco, Ines Mota, Wei-Tien Tai, Roberto Chiarle

Open access · greenAbstract readComment
In one paragraph

Article in Science translational medicine, 2018. 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
0.5field-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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Rafael B BlascoDepartment of Pathology, Children's Hospital Boston and Harvard Medical School, Boston, MA 02115 USA.ORCID 0000-0001-8025-0306
Enrico PatruccoDepartment of Molecular Biotechnology and Health Sciences, University of Torino, Torino 10126 Italy.ORCID 0000-0001-8060-5058
Ines MotaDepartment of Molecular Biotechnology and Health Sciences, University of Torino, Torino 10126 Italy.
Wei-Tien TaiDepartment of Pathology, Children's Hospital Boston and Harvard Medical School, Boston, MA 02115 USA.
Roberto ChiarleDepartment of Pathology, Children's Hospital Boston and Harvard Medical School, Boston, MA 02115 USA. roberto.chiarle@childrens.harvard.edu.ORCID 0000-0003-1564-8531
Boston Children's Hospital · USUniversity of Turin · IT

Funding

Mechanisms of resistance to ALK inhibitors in ALK-rearranged lymphomaR01CA196703 · NCI · BOSTON CHILDREN'S HOSPITAL · PI CHIARLE, ROBERTO · 2015 to 2025
$4.1M
NCI NIH HHS R01 CA196703
6 · The paper itself

Abstract

Physiologically relevant ALK (anaplastic lymphoma kinase) expression was not detected in human and mouse monocytes and macrophages, suggesting that the effects of bioactive compounds on stimulator of interferon genes (STING) activation may not depend on ALK.

Indexed as

Receptor Protein-Tyrosine KinasesSepsisAnaplastic Lymphoma KinaseAnimalsHumansMiceAnaplastic Lymphoma KinaseReceptor Protein-Tyrosine Kinases

Identifiers

PMID30541790
PMCPMC6459396
OpenAlexW2905261143

What OpenQuestion holds

Textmetadata
LicenceTDM
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.