Evidence map›Paper›PMID 23822506›Full record

ArticleChaos (Woodbury, N.Y.)2013

Phenotypic deconstruction of gene circuitry.

Jason G Lomnitz, Michael A Savageau

Abstract read
In one paragraph

Article in Chaos (Woodbury, N.Y.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Topological Environment in Genetic and Metabolic Networks.bioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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.

Jason G LomnitzDepartment of Biomedical Engineering, University of California, Davis, California 95616, USA.
Michael A Savageau

Funding

GENE CIRCUITS AND BIOCHEMICAL NETWORKSR01GM030054 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SAVAGEAU, MICHAEL A · 1985 to 2015
$3.2M
NIGMS NIH HHS R01 GM030054NIGMS NIH HHS R01-GM30054
6 · The paper itself

Abstract

It remains a challenge to obtain a global perspective on the behavioral repertoire of complex nonlinear gene circuits. In this paper, we describe a method for deconstructing complex systems into nonlinear sub-systems, based on mathematically defined phenotypes, which are then represented within a system design space that allows the repertoire of qualitatively distinct phenotypes of the complex system to be identified, enumerated, and analyzed. This method efficiently characterizes large regions of system design space and quickly generates alternative hypotheses for experimental testing. We describe the motivation and strategy in general terms, illustrate its use with a detailed example involving a two-gene circuit with a rich repertoire of dynamic behavior, and discuss experimental means of navigating the system design space.

Indexed as

Gene Regulatory NetworksFeedback, PhysiologicalNonlinear DynamicsPhenotype

Identifiers

PMID23822506
PMCPMC3695976

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.