Evidence map›Paper›PMID 39126473›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2024

Dynamic Live Cell Imaging of Budding Yeast Meiosis.

Hoa H Chuong, Jared M Evatt, Dean S Dawson

Abstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 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

3 authors.

Hoa H ChuongOklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Jared M EvattOklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Dean S DawsonOklahoma Medical Research Foundation, Oklahoma City, OK, USA. dawsond@omrf.org.

Funding

Centromere behaviors that promote proper chromosome segregation in meiosis and mitosisR35GM152165 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI DEAN S DAWSON · 2024 to 2026
$1.3M
NIGMS NIH HHS R35 GM152165
6 · The paper itself

Abstract

For over a century, major advances in understanding meiosis have come from the use of microscopy-based methods. Studies using the budding yeast, Saccharomyces cerevisiae, have made important contributions to our understanding of meiosis because of the facility with which budding yeast can be manipulated as a genetic model organism. In contrast, imaging-based approaches with budding yeast have been constrained by the small size of its chromosomes. The advent of advances in fluorescent chromosome tagging techniques has made it possible to use yeast more effectively for imaging-based approaches as well. This protocol describes live cell imaging methods that can be used to monitor chromosome movements throughout meiosis in living yeast cells.

Indexed as

MeiosisSaccharomyces cerevisiaeChromosomes, FungalMicroscopy, FluorescenceSaccharomycetalesBudding yeastFluorescence microscopyHardware triggeringInverted microscopeLight engineLive-cell imagingMeiosisMicrofluidicsSaccharomyces cerevisiae

Identifiers

PMID39126473
PMCPMC12704253

What OpenQuestion holds

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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.