Evidence map›Paper›PMID 38975021›Full record

ArticleMicrobial cell (Graz, Austria)2024

Expansion of metabolically labelled endocytic organelles and cytoskeletal cell structures in

Clirim Jetishi, Erina A Balmer, Bianca M Berger, Carmen Faso, Torsten Ochsenreiter

Abstract read
In one paragraph

Article in Microbial cell (Graz, Austria), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Clirim JetishiInstitute of Cell Biology, University of Bern Bern Switzerland.ORCID https://orcid.org/0000-0002-5632-7075
Erina A BalmerInstitute of Cell Biology, University of Bern Bern Switzerland.ORCID https://orcid.org/0000-0003-4815-2065
Bianca M BergerInstitute of Cell Biology, University of Bern Bern Switzerland.ORCID https://orcid.org/0000-0003-1009-4293
Carmen FasoInstitute of Cell Biology, University of Bern Bern Switzerland.ORCID https://orcid.org/0000-0002-1831-9365
Torsten OchsenreiterInstitute of Cell Biology, University of Bern Bern Switzerland.ORCID https://orcid.org/0000-0002-8846-8526

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding cellular ultrastructure is tightly bound to microscopic resolution and the ability to identify individual components at that resolution. Expansion microscopy has revolutionised this topic. Here we present and compare two protocols of ultrastructure expansion microscopy that allow for 4.5-fold mostly isotropic expansion and the use of antibodies, metabolic labelling, and DNA stains to demarcate individual regions such as the endoplasmic reticulum, the nuclei, the peripheral endocytic compartments as well as the ventral disc and the cytoskeleton in

Indexed as

cytoskeletonendocytosisendoplasmic reticulumexpansion microscopyGiardia lambliametabolic labellingsubcellular compartment

Identifiers

PMID38975021
PMCPMC11224680

What Socratic 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 Socratic graph.