Evidence map›Paper›PMID 11371625›Full record

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

Unexpected signals in a system subject to kinetic proofreading.

Z J Liu, H Haleem-Smith, H Chen, H Metzger

Open access · greenAbstract read
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 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 50 citations in OpenAlex.

  1. Regulation of IgE by T follicular helper cells.Journal of leukocyte biology · 2020
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. IgE and FcepsilonRI regulation.Clinical reviews in allergy & immunology · 2005
    Review
  10. Article
  11. Article
  12. Article
  13. Signaling cascades: escape from kinetic proofreading.Proceedings of the National Academy of Sciences of the United States of America · 2001
    Review
  14. Kinetic proofreading models for cell signaling predict ways to escape kinetic proofreading.Proceedings of the National Academy of Sciences of the United States of America · 2001
    Article
  15. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Z J LiuSection on Chemical Immunology, Arthritis and Rheumatism Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
H Haleem-Smith
H Chen
H Metzger
National Institute of Arthritis and Musculoskeletal and Skin Diseases · USNational Institutes of Health · US

Funding

CELL SURFACE RECEPTORS FOR IGEZ01AR041025 · NIAMS · ARTHRITIS, MUSCULOSKELETAL, SKIN DIS · PI METZGER, HENRY · 1986 to 2002
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6 · The paper itself

Abstract

When multivalent ligands attach to IgEs bound to the receptors with high affinity for IgE on mast cells, the receptors aggregate, tyrosines on the receptors become phosphorylated, and a variety of cellular responses are stimulated. Prior studies, confirmed here, demonstrated that the efficiency with which later events are generated from earlier ones is inversely related to the dissociation rate of the aggregating ligand. This finding suggests that the cellular responses are constrained by a "kinetic proofreading" regimen. We have now observed an apparent exception to this rule. Doses of the rapidly or slowly dissociating ligands that generated equivalent levels of tyrosine-phosphorylated receptors comparably stimulated a putatively distal event: transcription of the gene for monocyte chemoattractant protein 1. Possible explanations of this apparent anomaly were explored.

Indexed as

AnimalsAntibodies, MonoclonalCell DegranulationChemokine CCL2DactinomycinEnzyme PrecursorsGenes, fosHexosaminidasesImmunoglobulin EIntracellular Signaling Peptides and ProteinsKineticsLeukemia, Basophilic, AcuteLigandsMast CellsMicePhosphorylationAntibodies, MonoclonalChemokine CCL2DactinomycinEnzyme PrecursorsHexosaminidasesImmunoglobulin EIntracellular Signaling Peptides and ProteinsLigandsPhosphotyrosineProtein-Tyrosine KinasesProto-Oncogene Proteins c-fosReceptors, IgERNA, MessengerSyk KinaseSyk protein, mouseSyk protein, rat

Identifiers

PMID11371625
PMCPMC34661
OpenAlexW2015485550

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.