Evidence map›Paper›PMID 15184986›Full record

ReviewJournal of molecular medicine (Berlin, Germany)2004

Role of Id proteins in B lymphocyte activation: new insights from knockout mouse studies.

Manabu Sugai, Hiroyuki Gonda, Yukiko Nambu, Yoshifumi Yokota, Akira Shimizu

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of molecular medicine (Berlin, Germany), 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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  5. Article
  6. Article
  7. Article
  8. Review
  9. Regulation of the GABA cell phenotype in hippocampus of schizophrenics and bipolars.Proceedings of the National Academy of Sciences of the United States of America · 2007
    Article
  10. Ott1(Rbm15) has pleiotropic roles in hematopoietic development.Proceedings of the National Academy of Sciences of the United States of America · 2007
    Article
  11. Article
  12. Article
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

5 authors at 3 institutions in 1 country.

Manabu SugaiCenter for Molecular Biology and Genetics, Kyoto University, 53 Shogoin-Kawahara-cho, Sakyo-ku, 606-8507 Kyoto, Japan. msugai@virus.kyoto-u.ac.jp
Hiroyuki Gonda
Yukiko Nambu
Yoshifumi Yokota
Akira Shimizu
Kyoto University · JPKyoto University Hospital · JPUniversity of Fukui · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Id (inhibitor of differentiation) proteins play important roles in cell differentiation, cell cycle control, and apoptosis. They act as negative regulators of basic helix-loop-helix-type transcription factors, which positively regulate differentiation of various cell types. Id proteins work to block B lymphocyte (B cell) maturation at an early differentiation step, as demonstrated by gain-of-function studies. In recent years a series of gene-targeted mice lacking different Ids have been generated. Analyses of these gene-targeted mice provide information useful for understanding the physiological roles of Ids in B cell biology. Id3 is required for proper B cell functions and acts by controlling the cell cycle. Upon B cell activation, Id2 acts as a negative regulator to prevent potentially harmful effects brought about by excessive immunological reactions; one of its special roles is to maintain low serum concentrations of immunoglobulin E (IgE). The Id2 protein does this by antagonizing E2A and Pax5 activities, both of which are required for proper B cell activation. This review presents several new insights into B cell differentiation and activation programs and the physiological role of Id proteins in B cell activation.

Indexed as

AICDA (Activation-Induced Cytidine Deaminase)AnimalsBasic Helix-Loop-Helix ProteinsB-LymphocytesCell CycleCytidine DeaminaseDNA-Binding ProteinsImmunoglobulin Class SwitchingImmunoglobulin EInhibitor of Differentiation Protein 2Inhibitor of Differentiation ProteinsLymphocyte ActivationMiceMice, KnockoutNeoplasm ProteinsPAX5 Transcription FactorAICDA (Activation-Induced Cytidine Deaminase)Basic Helix-Loop-Helix ProteinsCytidine DeaminaseDNA-Binding ProteinsID3 protein, humanIdb2 protein, mouseImmunoglobulin EInhibitor of Differentiation Protein 2Inhibitor of Differentiation ProteinsNeoplasm ProteinsPax5 protein, mousePAX5 Transcription FactorRepressor ProteinsTcf3 protein, mouseTranscription FactorsTransforming Growth Factor beta

Identifiers

PMID15184986
OpenAlexW2034654093

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.