Evidence map›Paper›PMID 16549799›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2006

An evolutionarily mobile antigen receptor variable region gene: doubly rearranging NAR-TcR genes in sharks.

Michael F Criscitiello, Mark Saltis, Martin F Flajnik

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

52 citing papers in PubMed, 104 citations in OpenAlex.

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  13. A novel PD-L1-targeted shark VMolecular therapy oncolytics · 2022
    Article
  14. Article
  15. The immunoglobulins of cartilaginous fishes.Developmental and comparative immunology · 2021
    Review
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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

3 authors at 2 institutions in 1 country.

Michael F CriscitielloDepartment of Microbiology and Immunology, University of Maryland, Howard Hall, Suite 324, 660 West Redwood Street, Baltimore, MD 21201-1559, USA.
Mark Saltis
Martin F Flajnik
University of Maryland, Baltimore · USNational Aquarium · US

Funding

Origins of T Helper Cell Function in Adaptive ImmunityF32AI056963 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI CRISCITIELLO, MICHAEL FREDERICK · 2003 to 2005
$131k
NIAID NIH HHS F32 AI056963
6 · The paper itself

Abstract

Distinctive Ig and T cell receptor (TcR) chains define the two major lineages of vertebrate lymphocyte yet similarly recognize antigen with a single, membrane-distal variable (V) domain. Here we describe the first antigen receptor chain that employs two V domains, which are generated by separate VDJ gene rearrangement events. These molecules have specialized "supportive" TcRdeltaV domains membrane-proximal to domains with most similarity to IgNAR V. The ancestral NAR V gene encoding this domain is hypothesized to have recombined with the TRD locus in a cartilaginous fish ancestor >200 million years ago and encodes the first V domain shown to be used in both Igs and TcRs. Furthermore, these data support the view that gamma/delta TcRs have for long used structural conformations recognizing free antigen.

Indexed as

Evolution, MolecularAmino Acid SequenceAnimalsConserved SequenceGene Expression RegulationGene RearrangementGenetic VariationGenomeHumansLymphoid TissueMolecular Sequence DataOrgan SpecificityPhylogenyReceptors, Antigen, T-Cell, gamma-deltaSequence AlignmentSharksReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID16549799
PMCPMC1458790
OpenAlexW2027972989

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.