Evidence map›Paper›PMID 35563228›Full record

ReviewInternational journal of molecular sciences2022

Phosphoinositide 3-Kinases as Potential Targets for Thrombosis Prevention.

Natasha M Setiabakti, Pia Larsson, Justin R Hamilton

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
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

3 authors at 1 institution in 1 country.

Natasha M SetiabaktiAustralian Centre for Blood Diseases, Monash University, Melbourne, VIC 3004, Australia.ORCID 0000-0003-2017-561X
Pia LarssonAustralian Centre for Blood Diseases, Monash University, Melbourne, VIC 3004, Australia.
Justin R HamiltonAustralian Centre for Blood Diseases, Monash University, Melbourne, VIC 3004, Australia.ORCID 0000-0001-7554-6727
Australian Centre for HIV and Hepatitis Virology Research · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As integral parts of pathological arterial thrombi, platelets are the targets of pharmacological regimens designed to treat and prevent thrombosis. A detailed understanding of platelet biology and function is thus key to design treatments that prevent thrombotic cardiovascular disease without significant disruption of the haemostatic balance. Phosphoinositide 3-kinases (PI3Ks) are a group of lipid kinases critical to various aspects of platelet biology. There are eight PI3K isoforms, grouped into three classes. Our understanding of PI3K biology has recently progressed with the targeting of specific isoforms emerging as an attractive therapeutic strategy in various human diseases, including for thrombosis. This review will focus on the role of PI3K subtypes in platelet function and subsequent thrombus formation. Understanding the mechanisms by which platelet function is regulated by the various PI3Ks edges us closer toward targeting specific PI3K isoforms for anti-thrombotic therapy.

Indexed as

Phosphatidylinositol 3-KinasesThrombosisBlood PlateletsHumansPhosphatidylinositolsProtein IsoformsPhosphatidylinositol 3-KinasesPhosphatidylinositolsProtein Isoformsantiplatelet therapyphosphoinositide 3-kinasePI3Kplateletsthrombosis

Identifiers

PMID35563228
PMCPMC9105564
OpenAlexW4224996676

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.