Evidence map›Paper›PMID 22017429›Full record

ReviewImmunological reviews2011

How do pleiotropic kinase hubs mediate specific signaling by TNFR superfamily members?

Bärbel Schröfelbauer, Alexander Hoffmann

Open access · greenAbstract readReview
In one paragraph

Review in Immunological reviews, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Signaling via the NFκB system.Wiley interdisciplinary reviews. Systems biology and medicine · 2016
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. 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

2 authors at 1 institution in 1 country.

Bärbel SchröfelbauerSignaling Systems Laboratory, Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, CA 92093-0375, USA. bschroefelbauer@ucsd.edu
Alexander Hoffmann
University of California, San Diego · US

Funding

Information tranfer in NF-kappaB and MAPK pathwaysR01GM072024 · NIGMS · YALE UNIVERSITY · PI LEVCHENKO, ANDRE · 2004 to 2019
$3.9M
IKK:Biophysical basis of dynamic regulationR01CA141722 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GHOSH, GOURISANKAR, HOFFMANN, ALEXANDER · 2009 to 2013
$2.7M
Delays and variability in single-cell NFkB signalingR01GM089976 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HASTY, JEFF M, HOFFMANN, ALEXANDER · 2010 to 2013
$2.0M
NCI NIH HHS CA141722NCI NIH HHS R01 CA141722NIGMS NIH HHS R01 GM072024NIGMS NIH HHS R01 GM089976
6 · The paper itself

Abstract

Tumor necrosis factor receptor (TNFR) superfamily members mediate the cellular response to a wide variety of biological inputs. The responses range from cell death, survival, differentiation, proliferation, to the regulation of immunity. All these physiological responses are regulated by a limited number of highly pleiotropic kinases. The fact that the same signaling molecules are involved in transducing signals from TNFR superfamily members that regulate different and even opposing processes raises the question of how their specificity is determined. Regulatory strategies that can contribute to signaling specificity include scaffolding to control kinase specificity, combinatorial use of several signal transducers, and temporal control of signaling. In this review, we discuss these strategies in the context of TNFR superfamily member signaling.

Indexed as

Immunity, InnateAnimalsCell DeathCell DifferentiationCell ProliferationGene Expression RegulationHumansIntracellular Signaling Peptides and ProteinsMiceMolecular ChaperonesProtein BindingProtein IsoformsProtein KinasesReceptors, Tumor Necrosis FactorSignal TransductionSubstrate SpecificityIntracellular Signaling Peptides and ProteinsMolecular ChaperonesProtein IsoformsProtein KinasesReceptors, Tumor Necrosis FactorTumor Necrosis Factor-alpha

Identifiers

PMID22017429
PMCPMC3357464
OpenAlexW1916997990

What OpenQuestion holds

Textmetadata
LicenceTDM
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.