Evidence map›Paper›PMID 9144225›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1997

A novel pair of immunoglobulin-like receptors expressed by B cells and myeloid cells.

H Kubagawa, P D Burrows, M D Cooper

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed
11.6field-weighted citation impact, top 1% 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

96 citing papers in PubMed, 319 citations in OpenAlex.

  1. Article
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  7. Innate allorecognition in transplantation.The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2021
    Review
  8. Article
  9. Review
  10. Biological Effects of β-Glucans on Osteoclastogenesis.Molecules (Basel, Switzerland) · 2021
    Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Cellular Receptors of Amyloid β Oligomers (AβOs) in Alzheimer's Disease.International journal of molecular sciences · 2018
    Review

36 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

H KubagawaDepartment of Pathology, Division of Developmental and Clinical Immunology, University of Alabama, Birmingham, AL 35294-3300, USA.
P D Burrows
M D Cooper
Howard Hughes Medical Institute · USUniversity of Alabama · US

Funding

Comparison of B Cell Differentiation in Mice and HumansR37AI039816 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI COOPER, MAX DALE · 2001 to 2010
$3.8M
COMPARATIVE ONTOGENETIC APPROACH TO VACCINE STRATEGYR01AI039816 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI COOPER, MAX D · 1995 to 1999
–
T-CELL ANERGY LOSS TO A SUPERANTIGEN ON MRL-LPR/LPR MICEU01AI034568 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI COOPER, MAX D · 1993 to 1996
–
NIAID NIH HHS AI34568NIAID NIH HHS AI39816NIAID NIH HHS R01 AI039816NIAID NIH HHS R37 AI039816
6 · The paper itself

Abstract

An Fcalpha receptor probe of human origin was used to identify novel members of the Ig gene superfamily in mice. Paired Ig-like receptors, named PIR-A and PIR-B, are predicted from sequence analysis of the cDNAs isolated from a mouse splenic library. Both type I transmembrane proteins possess similar ectodomains with six Ig-like loops, but have different transmembrane and cytoplasmic regions. The predicted PIR-A protein has a short cytoplasmic tail and a charged Arg residue in the transmembrane region that, by analogy with the FcalphaR relative, suggests the potential for association with an additional transmembrane protein to form a signal transducing unit. In contrast, the PIR-B protein has an uncharged transmembrane region and a long cytoplasmic tail containing four potential immunoreceptor tyrosine-based inhibitory motifs. These features are shared by the related killer inhibitory receptors. PIR-A proteins appear to be highly variable, in that predicted peptide sequences differ for seven randomly selected PIR-A clones, whereas PIR-B cDNA clones are invariant. Southern blot analysis with PIR-B and PIR-A-specific probes suggests only one PIR-B gene and multiple PIR-A genes. The PIR-A and PIR-B genes are expressed in B lymphocytes and myeloid lineage cells, wherein both are expressed simultaneously. The characteristics of the highly-conserved PIR-A and PIR-B genes and their coordinate cellular expression suggest a potential regulatory role in humoral, inflammatory, and allergic responses.

Indexed as

Chromosome MappingChromosomes, Human, Pair 19Amino Acid SequenceAnimalsB-LymphocytesDNADNA, ComplementaryGene ExpressionGene LibraryGenetic MarkersGenetic VariationHematopoietic Stem CellsHumansMiceMice, Inbred BALB CMolecular Sequence DataDNADNA, ComplementaryGenetic MarkersPira1 protein, mousePira2 protein, mousePira3 protein, mousePira4 protein, mousePira5 protein, mousePira6 protein, mousePira7 protein, mousePirb protein, mouseReceptors, Immunologic

Identifiers

PMID9144225
PMCPMC24666
OpenAlexW2158449767

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.