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Updated: Jun 8, 2026

A Pipeline to Characterize Structural Heart Defects in the Fetal Mouse
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Imaging modalities to assess structural birth defects in mutant mouse models.

Kimimasa Tobita1, Xiaoqin Liu, Cecilia W Lo

  • 1Department of Developmental Biology, University of Pittsburgh, Pennsylvania 15224, USA. kit3@pitt.edu

Birth Defects Research. Part C, Embryo Today : Reviews
|September 23, 2010
PubMed
Summary

Advanced imaging techniques like ultrasound biomicroscopy and micro-MRI enable rapid phenotyping of structural birth defects (SBDs) in animal models. These methods allow detailed, noninvasive assessment of fetal development and detection of various SBDs.

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Area of Science:

  • Developmental Biology
  • Medical Imaging
  • Toxicology

Background:

  • Traditional assessment of structural birth defects (SBDs) in animal models involves invasive necropsy and histology.
  • These methods are time-consuming and do not allow for longitudinal studies of fetal development.

Purpose of the Study:

  • To review the application of advanced imaging technologies for the rapid phenotyping of SBDs in rodent embryos and fetuses.
  • To highlight the utility of these technologies in detecting a wide range of structural abnormalities.

Main Methods:

  • Review of recent advances in imaging technologies including ultra-high frequency ultrasound biomicroscopy, optical coherence tomography, micro-CT, and micro-MRI.
  • Discussion of the application of these modalities for noninvasive, in utero assessment of fetal anatomy and cardiovascular function.

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Last Updated: Jun 8, 2026

A Pipeline to Characterize Structural Heart Defects in the Fetal Mouse
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Published on: December 16, 2022

Murine Fetal Echocardiography
08:04

Murine Fetal Echocardiography

Published on: February 15, 2013

Fetal Mouse Cardiovascular Imaging Using a High-frequency Ultrasound (30/45MHZ) System
07:34

Fetal Mouse Cardiovascular Imaging Using a High-frequency Ultrasound (30/45MHZ) System

Published on: May 5, 2018

Main Results:

  • Advanced imaging modalities permit detailed assessment of organ and tissue structure in developing rodent embryos and fetuses.
  • Ultrasound biomicroscopy allows for noninvasive, longitudinal tracking of fetal development and cardiovascular assessment.
  • These technologies facilitate the detection of a broad spectrum of SBDs.

Conclusions:

  • State-of-the-art imaging technologies offer efficient and detailed methods for SBD phenotyping in preclinical research.
  • These noninvasive techniques can replace or supplement traditional methods, enabling longitudinal studies and early detection of developmental abnormalities.