Evidence map›Paper›PMID 42681388›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Analysis of Relative Telomere Length and mtDNA Content in Individual Oocytes and Embryos by Quantitative Real-Time PCR (qPCR).

Yasmyn E Winstanley, Darryl L Russell, Rebecca L Robker

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Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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.

Yasmyn E WinstanleyRobinson Research Institute, College of Health, Adelaide University, Adelaide, SA, Australia.
Darryl L RussellRobinson Research Institute, College of Health, Adelaide University, Adelaide, SA, Australia.
Rebecca L RobkerRobinson Research Institute, College of Health, Adelaide University, Adelaide, SA, Australia. rebecca.robker@adelaide.edu.au.ORCID http://orcid.org/0000-0002-1538-4604

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oocytes and embryos are highly susceptible to intrinsic and extrinsic stressors, making assays for biomarkers of embryo quality of high importance. This has been technically challenging due to the very small amounts of material in embryos, leading to the use of assays requiring pooled embryos which mask inter-embryo variability. This protocol details a qPCR assay to analyze relative telomere lengths and mtDNA content in individual oocytes and embryos. Each is singly collected and lysed in a minimal volume, then qPCR is used to independently amplify two nuclear (telomere and Rn18S) and one mitochondrial DNA sequence for quantification of relative telomere length or mtDNA content that is normalized for cell number by the reference gene. This methodology enables robust and precise measurements of these molecular biomarkers in physiological contexts where tissue availability is limited. Importantly, this assay allows detection of the natural variability in mtDNA and telomeric DNA content between individual oocytes and embryos.

Indexed as

DNA, MitochondrialEmbryo, MammalianOocytesReal-Time Polymerase Chain ReactionTelomereTelomere HomeostasisAnimalsFemaleMiceDNA, MitochondrialEmbryoMitochondrial DNAMouseOocyteqPCRTelomere

Identifiers

PMID42681388

What OpenQuestion holds

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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.