Evidence map›Paper›PMID 15303567›Full record

ReviewLupus2004

T-lymphocyte signalling in systemic lupus erythematosus: a lipid raft perspective.

E C Jury, P S Kabouridis

Open access · greenAbstract readReview
In one paragraph

Review in Lupus, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Pre-organized landscape of T cell surface.Frontiers in immunology · 2023
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
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  12. 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

2 authors at 2 institutions in 1 country.

E C JuryCentre for Rheumatology, Royal Free and University College Medical School, London, UK. e.jury@ucl.ac.uk
P S Kabouridis
Queen Mary University of London · GBThe Royal Free Hospital · GB

Funding

Wellcome Trust 058408
6 · The paper itself

Abstract

In the last few years it has become clear that in cells of the immune system, specialized microdomains present in the plasma membrane, called lipid rafts, have been found to play a central role in regulating signalling by immune receptors. Recent studies have looked at whether lipid rafts may be connected to the abnormalities in signalling seen in T lymphocytes isolated from patients with systemic lupus erythematosus (SLE). These early findings show that in SLE T cells, the expression and protein composition of lipid rafts is different when compared with normal T cells. These results also demonstrate changes in the function and localization of critical signalling molecules such as the LCK tyrosine kinase and the CD45 tyrosine phosphatase.

Indexed as

Signal TransductionG(M1) GangliosideHumansIntracellular Signaling Peptides and ProteinsLupus Erythematosus, SystemicLymphocyte Specific Protein Tyrosine Kinase p56(lck)Membrane ProteinsPhosphoproteinsT-LymphocytesG(M1) GangliosideIntracellular Signaling Peptides and ProteinsLymphocyte Specific Protein Tyrosine Kinase p56(lck)Membrane ProteinsPhosphoproteinsPTPRCAP protein, human

Identifiers

PMID15303567
PMCPMC2603271
OpenAlexW2080179461

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.