Evidence map›Paper›PMID 26059695›Full record

ArticleScientific reports2015

Investigation of the subcellular architecture of L7 neurons of Aplysia californica using magnetic resonance microscopy (MRM) at 7.8 microns.

Choong H Lee, Jeremy J Flint, Brian Hansen, Stephen J Blackband

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
  2. Review
  3. Article
  4. Article
  5. Article
  6. An Introduction to Kurtosis Fractional Anisotropy.AJNR. American journal of neuroradiology · 2019
    Review
  7. Article
  8. Low-temperature magnetic resonance imaging with 2.8 μm isotropic resolution.Journal of magnetic resonance (San Diego, Calif. : 1997) · 2018
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Micron-scale magnetic resonance imaging of both liquids and solids.Journal of magnetic resonance (San Diego, Calif. : 1997) · 2015
    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

4 authors.

Choong H Lee1] Department of Neuroscience, University of Florida College of Medicine, Gainesville, FL; 32611 [2] Mcknight Brain Institute, University of Florida, Gainesville, FL; 32611.
Jeremy J Flint1] Department of Neuroscience, University of Florida College of Medicine, Gainesville, FL; 32611 [2] Mcknight Brain Institute, University of Florida, Gainesville, FL; 32611.
Brian HansenCenter of Functionally Integrative Neuroscience (CFIN), Aarhus University, 8000 Aarhus C, Denmark.
Stephen J Blackband1] Department of Neuroscience, University of Florida College of Medicine, Gainesville, FL; 32611 [2] Mcknight Brain Institute, University of Florida, Gainesville, FL; 32611 [3] National High Magnetic Field Laboratory, Tallahassee, FL; 32310.

Funding

Development of MR Microscopy at the Cellular LevelR01EB012874 · NIBIB · UNIVERSITY OF FLORIDA · PI BLACKBAND, STEPHEN J. · 2010 to 2013
$2.1M
Console upgrade for microimaging and solid state NMR spectroscopy at 600 MHzS10RR031637 · NCRR · UNIVERSITY OF FLORIDA · PI LONG, JOANNA R · 2011 to 2011
$450k
NCRR NIH HHS S10 RR031637NCRR NIH HHS S10RR031637NIBIB NIH HHS 1R01EB012874NIBIB NIH HHS R01 EB012874
6 · The paper itself

Abstract

Magnetic resonance microscopy (MRM) is a non-invasive diagnostic tool which is well-suited to directly resolve cellular structures in ex vivo and in vitro tissues without use of exogenous contrast agents. Recent advances in its capability to visualize mammalian cellular structure in intact tissues have reinvigorated analytical interest in aquatic cell models whose previous findings warrant up-to-date validation of subcellular components. Even if the sensitivity of MRM is less than other microscopic technologies, its strength lies in that it relies on the same image contrast mechanisms as clinical MRI which make it a unique tool for improving our ability to interpret human diagnostic imaging through high resolution studies of well-controlled biological model systems. Here, we investigate the subcellular MR signal characteristics of isolated cells of Aplysia californica at an in-plane resolution of 7.8 μm. In addition, direct correlation and positive identification of subcellular architecture in the cells is achieved through well-established histology. We hope this methodology will serve as the groundwork for studying pathophysiological changes through perturbation studies and allow for development of disease-specific cellular modeling tools. Such an approach promises to reveal the MR contrast changes underlying cellular mechanisms in various human diseases, for example in ischemic stroke.

Indexed as

AnimalsAplysiaMagnetic Resonance ImagingMicroscopyNeurons

Identifiers

PMID26059695
PMCPMC4461915

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Registered trials

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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.