Evidence map›Paper›PMID 11493702›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2001

Identification of a family of Fc receptor homologs with preferential B cell expression.

R S Davis, Y H Wang, H Kubagawa, M D Cooper

Open access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed, 1 pooled it
11.3field-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

91 citing papers in PubMed, 1 synthesis or guideline pooled it, 215 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
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  6. Article
  7. Article
  8. Emerging Roles of Fc Receptor-Like 1 in Immunotherapy of Diffuse Large B-Cell Lymphoma.Biocell : official journal of the Sociedades Latinoamericanas de Microscopia Electronica ... et. al · 2025
    Article
  9. FcRL1, a New B-Cell-Activating Co-Receptor.International journal of molecular sciences · 2025
    Review
  10. Review
  11. CD4Lupus science & medicine · 2022
    Article
  12. Article
  13. Article
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  15. Article
  16. Article
  17. Galen medical journal · 2020
    Article
  18. Article
  19. Article
  20. Article

31 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

4 authors at 2 institutions in 1 country.

R S DavisDivisions of Hematology/Oncology, Department of Medicine, University of Alabama, Birmingham 35294-3300, USA.
Y H Wang
H Kubagawa
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
Studies of Paired Immunoglobulin-Like ReceptorsR01AI042127 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KUBAGAWA, HIROMI · 1998 to 2010
$2.2M
COMPARATIVE ONTOGENETIC APPROACH TO VACCINE STRATEGYR01AI039816 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI COOPER, MAX D · 1995 to 1999
–
NOVEL PAIR OF IMMUNOGLOBULIN LIKE RECEPTORSR21AI042127 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KUBAGAWA, HIROMI · 1998 to 1998
–
NIAID NIH HHS AI39816NIAID NIH HHS AI42127NIAID NIH HHS R01 AI039816NIAID NIH HHS R01 AI042127NIAID NIH HHS R37 AI039816
6 · The paper itself

Abstract

Investigation of human genome sequences with a consensus sequence derived from receptors for the Fc region of Igs (FcR) led to the identification of a subfamily of five Ig superfamily members that we term the Fc receptor homologs (FcRHs). The closely linked FcRH genes are located in a chromosome 1q21 region in the midst of previously recognized FcR genes. This report focuses on the FcRH1, FcRH2, and FcRH3 members of this gene family. Their cDNAs encode type I transmembrane glycoproteins with 3-6 Ig-like extracellular domains and cytoplasmic domains containing consensus immunoreceptor tyrosine-based activating and/or inhibitory signaling motifs. The five FcRH genes are structurally related, and their protein products share 28-60% extracellular identity with each other. They also share 15-31% identity with their closest FcR relatives. The FcRH genes are expressed primarily, although not exclusively, by mature B lineage cells. Their conserved structural features, patterns of cellular expression, and the inhibitory and activating signaling potential of their transmembrane protein products suggest that the members of this FcRH multigene family may serve important regulatory roles in normal and neoplastic B cell development.

Indexed as

Multigene FamilyAmino Acid SequenceBlotting, NorthernB-LymphocytesChromosome MappingChromosomes, Human, Pair 1Chromosomes, Human, Pair 19Consensus SequenceDNA, ComplementaryHematologic NeoplasmsHumansImmunoglobulin Fc FragmentsMolecular Sequence DataNeoplasm ProteinsOrgan SpecificityPhylogenyDNA, ComplementaryImmunoglobulin Fc FragmentsNeoplasm ProteinsProtein IsoformsReceptors, Fc

Identifiers

PMID11493702
PMCPMC55528
OpenAlexW2052279754

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.