Hargun Sohi1, Seth Ruffins1, Yang
Chai2, Scott Fraser1, Russell Jacobs3
1Caltech; 2USC; 3Caltech,
Microscopic
MRI (μMRI) is an emerging technique for high-throughput phenotyping of
transgenic mouse embryos, and is capable of visualizing abnormalities in
craniofacial development. μMRI methods rely on reduction of the tissue
T1 relaxation time by penetration of a gadolinium chelate contrast
agent. The use of contrast agents is
aimed at reducing the T1 relaxation time of the sample thus permitting a
decrease in acquisition scan time, and/or increase in image signal-to-noise
ratio (SNR), and/or increase in spatial resolution. In this work we apply
these technologies to delineating changes in a murine cleft palate model
system.