Evidence map›Paper›PMID 23906926›Full record

ReviewCurrent opinion in biotechnology2013

Towards high resolution analysis of metabolic flux in cells and tissues.

James K Sims, Sara Manteiga, Kyongbum Lee

Abstract readReview
In one paragraph

Review in Current opinion in biotechnology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
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.

James K SimsDepartment of Chemical and Biological Engineering, Tufts University, Medford, MA 02155, United States.
Sara Manteiga
Kyongbum Lee

Funding

Phenotype-Targeted Inference of Flux-Enzyme Correlations in Adipocyte MetabolismR56DK081768 · NIDDK · TUFTS UNIVERSITY MEDFORD · PI LEE, KYONGBUM · 2010 to 2011
$489k
Engineering an in vitro model of adipose tissue formation and metabolismR56DK088251 · NIDDK · TUFTS UNIVERSITY MEDFORD · PI LEE, KYONGBUM · 2010 to 2010
$205k
NIDDK NIH HHS R56 DK081768NIDDK NIH HHS R56DK081768NIDDK NIH HHS R56 DK088251NIDDK NIH HHS R56DK088251
6 · The paper itself

Abstract

Metabolism extracts chemical energy from nutrients, uses this energy to form building blocks for biosynthesis, and interconverts between various small molecules that coordinate the activities of cellular pathways. The metabolic state of a cell is increasingly recognized to determine the phenotype of not only metabolically active cell types such as liver, muscle, and adipose, but also other specialized cell types such as neurons and immune cells. This review focuses on methods to quantify intracellular reaction flux as a measure of cellular metabolic activity, with emphasis on studies involving cells of mammalian tissue. Two key areas are highlighted for future development, single cell metabolomics and noninvasive imaging, which could enable spatiotemporally resolved analysis and thereby overcome issues of heterogeneity, a distinctive feature of tissue metabolism.

Indexed as

MetabolismMetabolomicsAnimalsCellsGenomicsHumansMammalsMolecular ImagingOrgan SpecificitySingle-Cell AnalysisSpatio-Temporal Analysis

Identifiers

PMID23906926
PMCPMC3783555

What OpenQuestion holds

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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.