Evidence map›Paper›PMID 10835339›Full record

ReviewThe EMBO journal2000

Receptor recognition by gp130 cytokines.

J Bravo, J K Heath

Abstract readComparative StudyReview
In one paragraph

Review in The EMBO journal, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
–field-weighted citation impact
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

65 citing papers in PubMed.

  1. Article
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5 more citing papers are in PubMed but not listed here.

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.

J BravoMRC Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, UK.
J K Heath

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytokines of the gp130 family exert their diverse biological effects by formation of stable high affinity transmembrane receptor complexes that are characterized by the presence of the shared transmembrane signalling receptor gp130. Different gp130 ligands form signalling complexes that vary in both composition and stoichiometry. Analysis of the three-dimensional structure of selected ligands and receptor elements indicates that ligands display three topologically conserved receptor recognition epitopes that interact with complementary ligand recognition elements. The composition of the signalling complex and downstream biological responses is defined by the relative affinity of different receptor components for these epitopes. The detailed structure of receptor recognition epitopes indicates that the generation of small molecule cytokine mimetics may be a feasible objective.

Indexed as

Antigens, CDCytokine Receptor gp130CytokinesDimerizationDrug DesignEpitopesGrowth InhibitorsHuman Growth HormoneHumansInterleukin-6Leukemia Inhibitory FactorLigandsLymphokinesMembrane GlycoproteinsModels, MolecularMultigene FamilyAntigens, CDCytokine Receptor gp130CytokinesEpitopesGrowth InhibitorsHuman Growth HormoneIL6ST protein, humanInterleukin-6Leukemia Inhibitory FactorLIF protein, humanLigandsLymphokinesMembrane GlycoproteinsReceptors, CytokineReceptors, Somatotropin

Identifiers

PMID10835339
PMCPMC212748

What OpenQuestion holds

Textmetadata
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.