| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 4332262 | Brain Research | 2006 | 7 Pages | 
Abstract
												Hypoxic–ischemic encephalopathy (HIE) in neonates results in long-term disabilities. Stem cell therapy may offer an attractive treatment for HIE. Multipotent astrocytic stem cells (MASCs) from mice transplanted into a rat model of hypoxia–ischemia (HI) survived the transplantation and showed signs of migration towards the injured cortex. Some MASCs around the injured cortex differentiated into neuronal and astrocytic phenotypes. MASCs transplanted into non-ischemic pups survived but retained their astrocytic phenotype. These data suggest that transplanted MASCs can survive and differentiate into neurons and astrocytes in the post-injury milieu of the neonatal brain injured by HI.
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											Authors
												Tong Zheng, Candace Rossignol, Avital Leibovici, Kevin J. Anderson, Dennis A. Steindler, Michael D. Weiss, 
											