Evidence map›Paper›PMID 15869393›Full record

ReviewAnnual review of biophysics and biomolecular structure2005

Toward predictive models of mammalian cells.

Avi Ma'ayan, Robert D Blitzer, Ravi Iyengar

Abstract readReview
In one paragraph

Review in Annual review of biophysics and biomolecular structure, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. A systems approach to infectious disease.Nature reviews. Genetics · 2020
    Review
  5. Review
  6. Article
  7. Article
  8. A network-oriented perspective on cardiac calcium signaling.American journal of physiology. Cell physiology · 2012
    Review
  9. Merging systems biology with pharmacodynamics.Science translational medicine · 2012
    Review
  10. Article
  11. Article
  12. Systems pharmacology of complex diseases.Annals of the New York Academy of Sciences · 2011
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  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

3 authors.

Avi Ma'ayanDepartment of Pharmacology and Biological Chemistry, Mount Sinai School of Medicine, New York, NY 10029, USA. avi.maayan@mssm.edu
Robert D Blitzer
Ravi Iyengar

Funding

System Biology Center in New YorkP50GM071558 · NIGMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ZAPH, SUSANA NEVES · 2007 to 2017
$22.8M
MOLECULAR MECHANISM OF DESENSITIZATIONR01GM054508 · NIGMS · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI IYENGAR, SRINIVAS RAVI V · 1995 to 2016
$8.0M
Teaching biomedical and pharmacological trainees to produce FAIR data for AI & ML applicationsT32GM062754 · NIGMS · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI SCHLESSINGER, AVNER · 2001 to 2023
$6.2M
SIGNALING PATHWAYS INTERACTIONS AND MAMMARY TUMORR01CA081050 · NCI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI IYENGAR, SRINIVAS RAVI V · 2000 to 2004
$1.8M
NCI NIH HHS CA-81050NCI NIH HHS R01 CA081050NIGMS NIH HHS GM-54508NIGMS NIH HHS GM-62754NIGMS NIH HHS P50 GM071558NIGMS NIH HHS R01 GM054508NIGMS NIH HHS T32 GM062754
6 · The paper itself

Abstract

Progress in experimental and theoretical biology is likely to provide us with the opportunity to assemble detailed predictive models of mammalian cells. Using a functional format to describe the organization of mammalian cells, we describe current approaches for developing qualitative and quantitative models using data from a variety of experimental sources. Recent developments and applications of graph theory to biological networks are reviewed. The use of these qualitative models to identify the topology of regulatory motifs and functional modules is discussed. Cellular homeostasis and plasticity are interpreted within the framework of balance between regulatory motifs and interactions between modules. From this analysis we identify the need for detailed quantitative models on the basis of the representation of the chemistry underlying the cellular process. The use of deterministic, stochastic, and hybrid models to represent cellular processes is reviewed, and an initial integrated approach for the development of large-scale predictive models of a mammalian cell is presented.

Indexed as

Models, BiologicalAmino Acid MotifsAnimalsBiochemistryBiologyBiophysicsCluster AnalysisHumansInternetModels, TheoreticalSignal TransductionSoftware

Identifiers

PMID15869393
PMCPMC3035045

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.