Evidence map›Paper›PMID 19879266›Full record

ReviewFEBS letters2009

Qualitatively distinct phenotypes in the design space of biochemical systems.

Michael A Savageau, Rick A Fasani

Abstract readReview
In one paragraph

Review in FEBS letters, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. The best models of metabolism.Wiley interdisciplinary reviews. Systems biology and medicine · 2017
    Review
  5. Article
  6. Article
  7. Article
  8. Unrelated toxin-antitoxin systems cooperate to induce persistence.Journal of the Royal Society, Interface · 2015
    Article
  9. Article
  10. Article
  11. Molecular mechanisms of multiple toxin-antitoxin systems are coordinated to govern the persister phenotype.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  12. Article
  13. Article
  14. Design of the lac gene circuit revisited.Mathematical biosciences · 2011
    Review
  15. Biomedical engineering strategies in system design space.Annals of biomedical engineering · 2011
    Review
  16. Article
  17. Article
  18. Article
  19. 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.

Michael A SavageauDepartment of Biomedical Engineering, University of California, Davis, CA 95616-5294, USA. masavageau@ucdavis.edu
Rick A Fasani

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

Although characterization of the genotype has undergone revolutionary advances as a result of the successful genome projects, the chasm between our understanding of a fully characterized gene sequence and the phenotypic repertoire of the organism is as broad and deep as it was in the pre-genomic era. There are two fundamental unsolved problems that provide the context for the challenges in relating genotype to phenotype. We address one of these and describe a generic method for constructing a system design space in which qualitatively distinct phenotypes can be identified and counted, their relative fitness analyzed and compared, and their tolerance to change measured.

Indexed as

Gene Regulatory NetworksGenotypeModels, GeneticPhenotypeBacteriophage lambdaLysogeny

Identifiers

PMID19879266
PMCPMC2888490

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.