Evidence map›Paper›PMID 31636458›Full record

ArticleNature methods2019

A super-resolution platform for correlative live single-molecule imaging and STED microscopy.

V V G Krishna Inavalli, Martin O Lenz, Corey Butler, Julie Angibaud, Benjamin Compans, Florian Levet, Jan Tønnesen, Olivier Rossier, Gregory Giannone, Olivier Thoumine and 4 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature methods, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Structured light analogy of quantum squeezed states.Light, science & applications · 2024
    Article
  10. Architecture-driven quantitative nanoscopy maps cytoskeleton remodeling.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  11. Article
  12. Fluorescence microscopy shadow imaging for neuroscience.Frontiers in cellular neuroscience · 2024
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. STORM Super-Resolution Imaging of CBMethods in molecular biology (Clifton, N.J.) · 2023
    Article
  18. Super-Resolution Microscopy Opens New Doors to Life at the Nanoscale.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Review
  19. Article
  20. Event-triggered STED imaging.Nature methods · 2022
    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

14 authors.

V V G Krishna InavalliInterdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France.ORCID http://orcid.org/0000-0002-7100-0214
Martin O LenzInterdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France.ORCID http://orcid.org/0000-0002-1658-4368
Corey ButlerInterdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France.ORCID http://orcid.org/0000-0003-3677-9194
Julie AngibaudInterdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France.
Benjamin CompansInterdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France.ORCID http://orcid.org/0000-0001-7823-1499
Florian LevetInterdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France.ORCID http://orcid.org/0000-0002-4009-6225
Jan TønnesenInterdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France.ORCID http://orcid.org/0000-0003-3663-8463
Olivier RossierInterdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France.ORCID http://orcid.org/0000-0002-6932-931X
Gregory GiannoneInterdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France.
Olivier ThoumineInterdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France.
Eric HosyInterdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France.ORCID http://orcid.org/0000-0002-2479-5915
Daniel ChoquetInterdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France.ORCID http://orcid.org/0000-0003-4726-9763
Jean-Baptiste Sibarita *Interdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France. jean-baptiste.sibarita@u-bordeaux.fr.ORCID http://orcid.org/0000-0002-9920-7700
U Valentin Nägerl *Interdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France. valentin.nagerl@u-bordeaux.fr.ORCID http://orcid.org/0000-0001-6831-9008

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Super-resolution microscopy offers tremendous opportunities to unravel the complex and dynamic architecture of living cells. However, current super-resolution microscopes are well suited for revealing protein distributions or cell morphology, but not both. We present a super-resolution platform that permits correlative single-molecule imaging and stimulated emission depletion microscopy in live cells. It gives nanoscale access to the positions and movements of synaptic proteins within the morphological context of growth cones and dendritic spines.

Indexed as

AnimalsCells, CulturedFemaleHumansImage Processing, Computer-AssistedMiceMicroscopy, FluorescenceRatsRats, Sprague-DawleySingle Molecule Imaging

Identifiers

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.