Evidence map›Paper›PMID 42162540›Full record

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

Dynamic Imaging of Mouse Embryos and Cardiodynamics in Static Culture.

Andrew L Lopez, Irina V Larina

Abstract read
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In one paragraph

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.

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.

Andrew L LopezDepartment of Integrative Physiology, Baylor College of Medicine, Houston, TX, USA.
Irina V LarinaDepartment of Integrative Physiology, Baylor College of Medicine, Houston, TX, USA. larina@bcm.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The heart is a dynamic organ that undergoes rapid morphological and mechanical changes during early embryonic development. Characterizing these early moments is important for our understanding of proper embryonic development and the treatment of heart disease. Traditionally, tomographic imaging modalities and fluorescence-based microscopy are excellent approaches for visualizing structural features and gene expression patterns, respectively, and connecting aberrant gene programs to pathological phenotypes. However, these approaches typically require static samples or fluorescent markers, which can limit the amount of information we can derive from the dynamic and mechanical changes that regulate heart development. Optical coherence tomography (OCT) is unique in this context because it enables the acquisition of three-dimensional structural images and four-dimensional (3D + time) functional imaging of living mouse embryos without the need for fixation or contrast agents. In this chapter, we focus on how OCT can visualize heart morphology at different stages of development and provide cardiodynamic information to reveal the mechanical properties of the developing heart.

Indexed as

Embryo, MammalianHeartTomography, Optical CoherenceAnimalsEmbryo Culture TechniquesEmbryonic DevelopmentImaging, Three-DimensionalMiceCardiodynamic analysisCardiovascular developmentEmbryo cultureHeart morphogenesisLive imagingMouseOptical coherence tomography

Identifiers

PMID42162540

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.