Evidence map›Paper›PMID 24678775›Full record

ReviewExpert review of clinical immunology2014

The role of tyrosine kinases in systemic lupus erythematosus and their potential as therapeutic targets.

Wen-Hai Shao, Philip L Cohen

Open access · greenAbstract readReview
In one paragraph

Review in Expert review of clinical immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

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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

2 authors at 2 institutions in 1 country.

Wen-Hai ShaoDepartment of Medicine and Temple Autoimmunity Center, Section of Rheumatology, Temple University, Philadelphia, PA, USA.
Philip L Cohen
Temple College · USTemple University · US

Funding

A critical role of TAM receptors in autoimmune nephritisK01DK095067 · NIDDK · UNIVERSITY OF CINCINNATI · PI SHAO, WEN-HAI · 2013 to 2017
$647k
NIAID NIH HHS U19AI10822726NIDDK NIH HHS 1K01DK095067NIDDK NIH HHS K01 DK095067
6 · The paper itself

Abstract

The autoimmune disease systemic lupus erythematosus is characterized by loss of tolerance to nuclear antigens. Breakdown of tolerance is associated with alterations in T-cell and B-cell receptor signal transduction, including increased protein phosphorylation that may underlie pathogenesis and explain the characteristic hyperactivity of T and B cells and other immune cells in active disease. Tyrosine kinases play a central role in signaling processes in cells known to be important in the pathogenesis of autoimmune diseases. Considerable progress has been made in understanding the function of tyrosine kinases in immune cell signaling pathways. In this review, we will summarize the function of tyrosine kinases and their novel inhibitors from studies made in animal lupus models and systemic lupus erythematosus patients.

Indexed as

AnimalsB-LymphocytesHumansImmune SystemLupus Erythematosus, SystemicModels, ImmunologicalProtein Kinase InhibitorsProtein-Tyrosine KinasesSignal TransductionT-LymphocytesProtein Kinase InhibitorsProtein-Tyrosine Kinases

Identifiers

PMID24678775
PMCPMC4249585
OpenAlexW2133228420

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.