Evidence map›Paper›PMID 9743524›Full record

ArticleThe Journal of experimental medicine1998

Functional redundancy of the nuclear factor kappa B inhibitors I kappa B alpha and I kappa B beta.

J D Cheng, R P Ryseck, R M Attar, D Dambach, R Bravo

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

46 citing papers in PubMed, 105 citations in OpenAlex.

  1. Review
  2. Article
  3. APAP-Induced IκBβ/NFκB Signaling Drives Hepatic Il6 Expression and Associated Sinusoidal Dilation.Toxicological sciences : an official journal of the Society of Toxicology · 2022
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Anatomy of a negative feedback loop: the case of IκBα.Journal of the Royal Society, Interface · 2015
    Article
  13. Article
  14. Sustained hyperoxia-induced NF-κB activation improves survival and preserves lung development in neonatal mice.American journal of physiology. Lung cellular and molecular physiology · 2014
    Article
  15. IκBβ-mediated NF-κB activation confers protection against hyperoxic lung injury.American journal of respiratory cell and molecular biology · 2014
    Article
  16. NFκB function and regulation in cutaneous T-cell lymphoma.American journal of cancer research · 2013
    Review
  17. Article
  18. Article
  19. Celebrating 25 years of NF-κB research.Immunological reviews · 2012
    Article
  20. 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 1 institution in 1 country.

J D ChengDepartment of Oncology, Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08543-4000, USA.
R P Ryseck
R M Attar
D Dambach
R Bravo
Bristol-Myers Squibb (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transcription factor NF-kappaB is sequestered in the cytoplasm by the inhibitor proteins of the IkappaB family. Each member of the IkappaB exhibits structural and biochemical similarities as well as differences. In an effort to address the functional redundancy of two closely related IkappaB molecules, IkappaBalpha and IkappaBbeta, we generated knock-in mice by replacing the IkappaBalpha gene with the IkappaBbeta gene. The knock-in mice do not express IkappaBalpha, but express a T7-tagged IkappaBbeta under the promoter and regulatory sequence of ikba. Unlike the IkappaBalpha-deficient mice, which display severe postnatal developmental defects and die by postnatal day 8, homozygous knock-in mice survive to adulthood, are fertile, and exhibit no apparent abnormalities. Furthermore, thymocytes and embryonic fibroblasts from the knock-in animals exhibit an inducible NF-kappaB response similar to that of wild-type animals. These results indicate that IkappaBalpha and IkappaBbeta share significant similarities in their biochemical activity, and that they acquired their different functions from divergent expression patterns during evolution.

Indexed as

I-kappa B ProteinsAnimalsDNA-Binding ProteinsEmbryo, MammalianFemaleFibroblastsGenetic VectorsMaleMiceMice, Inbred ICRMice, KnockoutMice, TransgenicNF-kappa BNF-KappaB Inhibitor alphaRecombination, GeneticSequence DeletionDNA-Binding ProteinsI kappa B beta proteinI-kappa B ProteinsNF-kappa BNF-KappaB Inhibitor alphaNfkbia protein, mouse

Identifiers

PMID9743524
PMCPMC2212550
OpenAlexW2017103994

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.