Evidence map›Paper›PMID 2138787›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1990

Genomic organization of mouse Fc gamma receptor genes.

A Kulczycki, J Webber, H A Soares, M D Onken, J A Thompson, D D Chaplin, D Y Loh, J P Tillinghast

Abstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1990. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Identification of a family of Fc receptor homologs with preferential B cell expression.Proceedings of the National Academy of Sciences of the United States of America · 2001
    Article
  3. Article
  4. Article
  5. 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

8 authors.

A KulczyckiDepartment of Medicine, Washington University School of Medicine, Saint Louis, MO 63110.
J Webber
H A Soares
M D Onken
J A Thompson
D D Chaplin
D Y Loh
J P Tillinghast

Funding

BOVINE IGG AND HUMAN IMMUNOLOGIC RESPONSES &DISEASESR01AI024005 · NIAID · WASHINGTON UNIVERSITY · PI KULCZYCKI, ANTHONY · 1987 to 1989
–
NIAID NIH HHS AI 24005
6 · The paper itself

Abstract

We have isolated and characterized the gene coding for the mouse Fc receptor that is termed Fc gamma RIIa. The gene contains five exons and spans approximately 9 kilobases. Unlike most members of the immunoglobulin gene superfamily, this gene utilizes multiple exons to encode its leader peptide. The first exon encodes the hydrophobic region of the signal sequence; the second exon, which contains only 21 base pairs, encodes a segment of the signal peptidase recognition site; and the beginning of the third exon encodes the predicted site of peptidase cleavage. The third and fourth exons each code for immunoglobulin-like extracellular domains. The fifth exon encodes the hydrophobic transmembrane domain and the cytoplasmic tail. Partial characterization of the Fc gamma RIIb gene indicates that it also contains multiple leader exons, including a 21-base-pair exon and two exons coding for homologous immunoglobulin-like extracellular domains. However, the Fc gamma RIIb gene uses four exons to encode its intracytoplasmic region. Analysis using contour-clamped homogeneous electric field (CHEF) gels indicates that the Fc gamma RIIa and Fc gamma RIIb genes are linked within 160 kilobases on mouse chromosome 1.

Indexed as

Multigene FamilyAmino Acid SequenceAnimalsAntigens, DifferentiationBase SequenceCloning, MolecularExonsMiceMolecular Sequence DataReceptors, FcReceptors, IgGRestriction MappingRNA SplicingSequence Homology, Nucleic AcidAntigens, DifferentiationReceptors, FcReceptors, IgG

Identifiers

PMID2138787
PMCPMC53790

What OpenQuestion holds

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Registered trials

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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.