Evidence map›Paper›PMID 38633103›Full record

ArticleBiomedical optics express2024

Fast volumetric multifocus structured illumination microscopy of subcellular dynamics in living cells.

Maximilian Lukas Senftleben, Antone Bajor, Eduardo Hirata, Sara Abrahamsson, Hjalmar Brismar

Abstract read
In one paragraph

Article in Biomedical optics express, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Maximilian Lukas SenftlebenDepartment of Applied Physics, KTH Royal Institute of Technology, Science for Life Laboratory, Stockholm, Sweden.ORCID https://orcid.org/0000-0002-9443-8251
Antone BajorBaskin School of Engineering, University of California Santa Cruz, 1156 High Street, Santa Cruz, 95064, CA, USA.
Eduardo HirataDepartment of Applied Physics, KTH Royal Institute of Technology, Science for Life Laboratory, Stockholm, Sweden.ORCID https://orcid.org/0000-0002-1016-2447
Sara AbrahamssonBaskin School of Engineering, University of California Santa Cruz, 1156 High Street, Santa Cruz, 95064, CA, USA.
Hjalmar BrismarDepartment of Applied Physics, KTH Royal Institute of Technology, Science for Life Laboratory, Stockholm, Sweden.ORCID https://orcid.org/0000-0003-0578-4003

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studying the nanoscale dynamics of subcellular structures is possible with 2D structured illumination microscopy (SIM). The method allows for acquisition with improved resolution over typical widefield. For 3D samples, the acquisition speed is inherently limited by the need to acquire sequential two-dimensional planes to create a volume. Here, we present a development of multifocus SIM designed to provide high volumetric frame rate by using fast synchronized electro-optical components. We demonstrate the high volumetric imaging capacity of the microscope by recording the dynamics of microtubule and endoplasmatic reticulum in living cells at up to 2.3 super resolution volumes per second for a total volume of 30 × 30 × 1.8 µm

Identifiers

PMID38633103
PMCPMC11019691

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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.