Evidence map›Paper›PMID 40736798›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

Nuclear Tracking During Early Embryonic Divisions.

Yunan Ye, Hayden A Homer

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2025. 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

2 authors.

Yunan YeThe Christopher Chen Oocyte Biology Research Laboratory, Centre for Clinical Research, The University of Queensland, Herston, QLD, Australia.
Hayden A HomerThe Christopher Chen Oocyte Biology Research Laboratory, Centre for Clinical Research, The University of Queensland, Herston, QLD, Australia. h.homer@uq.edu.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Positioning of the largest organelle, the nucleus, provides important cues for the geometry of cell divisions and cell fate determination. A primary function of nuclear positioning is to determine the spindle position and cleavage plane localization during cell division. Thus, centrally located nuclei lead to symmetrical divisions typical of mitosis, and off-center spindles culminate in symmetry-breaking as in mammalian oocytes. More recently, nuclear positioning has also been implicated in regulating mechanotransduction and gene expression in mouse oocytes. In human embryos, equal blastomere size arising from symmetrical cleavage-stage divisions is associated with favorable developmental outcomes, whereas off-center nuclear positioning affects division symmetry that can derail development. Therefore, investigating the mechanisms involved in nuclear positioning is critical for understanding embryo biology and the basis for clinical infertility. Here, we describe a method involving confocal imaging for performing nuclear tracking during early embryonic divisions in mouse embryos.

Indexed as

Cell DivisionCell NucleusEmbryo, MammalianIntravital MicroscopyAnimalsEmbryo Culture TechniquesEmbryonic DevelopmentFemaleGene Expression Regulation, DevelopmentalMaleMechanotransduction, CellularMiceMicroscopy, ConfocalPregnancySpindle ApparatusEmbryoNuclear positioningNuclear trackingOocyteTime-lapse imagingTrackMate

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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.