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Related Concept Videos

Gastrulation01:56

Gastrulation

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Gastrulation establishes the three primary tissues of an embryo: the ectoderm, mesoderm, and endoderm. This developmental process relies on a series of intricate cellular movements, which in humans transforms a flat, “bilaminar disc” composed of two cell sheets into a three-tiered structure. In the resulting embryo, the endoderm serves as the bottom layer, and stacked directly above it is the intermediate mesoderm, and then the uppermost ectoderm. Respectively, these tissue strata...
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Related Experiment Video

Updated: Mar 22, 2026

Mouse Embryonic Development in a Serum-free Whole Embryo Culture System
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Early Development of the Mouse Morphome.

Joseph A Hampel1, Jacob Rinkinen, Jonathan R Peterson

  • 1*Unit for Laboratory Animal Medicine†Department of Surgery, University of Michigan Medical School, Ann Arbor, MI.

The Journal of Craniofacial Surgery
|April 22, 2016
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Summary
This summary is machine-generated.

This study developed a microCT imaging protocol for longitudinal animal studies. The refined method provides reliable, objective data for morphomic analysis, advancing research in frailty and bone health.

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Area of Science:

  • Biomedical Imaging
  • Osteoporosis Research
  • Animal Models

Background:

  • Analytical morphomics uses quantitative data from CT scans to assess patient frailty.
  • Current morphomics studies are retrospective, limiting controlled prospective research.
  • Developing animal models is crucial for prospective, well-controlled morphomics studies.

Purpose of the Study:

  • To establish an in vivo microCT protocol for longitudinal, whole-body imaging in research animals.
  • To enable morphomic analyses of bone structure and density.
  • To create a platform for testing hypotheses derived from human clinical morphomics.

Main Methods:

  • Phantom studies were conducted on two microCT systems (Inveon and CT120) to evaluate tissue radiodensity and system performance.
  • A phantom-immobilization device was designed and tested using phantoms and an ovariectomized (OVX) mouse model.
  • Data analysis involved assessing scan consistency, the impact of field-of-view objects, and the utility of using the middle 80% of slices.

Main Results:

  • The Inveon system demonstrated greater z-axis consistency than the CT120; slice-by-slice calibration reduced variability.
  • Using the middle 80% of slices significantly decreased data variability on both systems.
  • Bone mineral density calibration with a phantom improved estimates, and the OVX mouse model was validated by body weight and uterine mass comparisons.

Conclusions:

  • A refined microCT protocol was developed for acquiring reliable, objective data in research animals.
  • This protocol establishes a foundation for animal morphomics research.
  • The platform will facilitate testing hypotheses generated from human clinical morphomics studies.