Evidence map›Paper›PMID 1834376›Full record

ArticleClinical and experimental immunology1991

Fc gamma RII alpha: sequencing of the ligand binding domain in systemic lupus erythematosus patients.

E C Jazwinska, J L Banyer, P A Gatenby, S W Serjeantson

Abstract read
In one paragraph

Article in Clinical and experimental immunology, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

E C JazwinskaDivision of Clinical Sciences, John Curtin School of Medical Research, Australian National University, Canberra.
J L Banyer
P A Gatenby
S W Serjeantson

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The receptor for the Fc portion of IgG (Fc gamma R) is involved in the slow clearance of immune complexes. To perform this role it must be cross-linked by IgG bound in its extracellular domains. It has been suggested that defective Fc gamma R-mediated clearance of immune complexes may play a role in the pathogenesis of autoimmune connective tissue disorders. We have sequenced DNA encoding the second extracellular domain of Fc gamma RII alpha in six patients with SLE, to investigate whether point mutations may be responsible for encoding a defect in the IgG binding capacity of the receptor. We were able to identify the point mutation which discriminates high and low responder genotypes but found no other change from the published DNA sequence for this region.

Indexed as

Antigens, DifferentiationBase SequenceBinding SitesHumansLupus Erythematosus, SystemicMolecular Sequence DataOligonucleotidesPolymerase Chain ReactionPolymorphism, GeneticReceptors, FcReceptors, IgGAntigens, DifferentiationOligonucleotidesReceptors, FcReceptors, IgG

Identifiers

PMID1834376
PMCPMC1554141

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.