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Fat cells heal skull defects in mice, Stanford research shows

elopmental biology of skeleton formation during embryogenesis, and figuring out how to release those same coaching signals in children and adults.

"These cells are readily available, easily expandable and they don't require gene therapy to work," he added. "In the future we may not have to leave the operating room or the patient's bedside to use cell-based therapies for skeletal regenerative medicine."


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Contact: Robert Dicks
rdicks@stanfordmed.org
650-497-8364
Stanford University Medical Center
4-May-2004


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