| Distinct contribution of human cord blood-derived endothelial colony forming cells to liver and gut in a fetal sheep model. | |
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MedLine Citation:
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PMID: 22488442 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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CONCLUSION: ECFC inherently constitute a potential source of cells for the treatment of intestinal diseases, but strategies to increase the numbers of ECFC persisting within the hepatic parenchyma are needed in order to enhance ECFC therapeutic potential for this organ. |
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Authors:
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Joshua A Wood; Evan Colletti; Laura E Mead; David Ingram; Christopher D Porada; Esmail D Zanjani; Mervin C Yoder; Graça Almeida-Porada |
Publication Detail:
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Type: Journal Article; Research Support, N.I.H., Extramural Date: 2012-08-02 |
Journal Detail:
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Title: Hepatology (Baltimore, Md.) Volume: 56 ISSN: 1527-3350 ISO Abbreviation: Hepatology Publication Date: 2012 Sep |
Date Detail:
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Created Date: 2012-08-29 Completed Date: 2012-10-30 Revised Date: 2013-05-20 |
Medline Journal Info:
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Nlm Unique ID: 8302946 Medline TA: Hepatology Country: United States |
Other Details:
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Languages: eng Pagination: 1086-96 Citation Subset: IM |
Copyright Information:
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Copyright © 2012 American Association for the Study of Liver Diseases. |
Affiliation:
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Department of Animal Biotechnology, University of Nevada, Reno, NV, USA. |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Animals Cell Movement* Endothelial Cells / physiology*, transplantation Fetal Blood* Humans Intestines / cytology* Liver / cytology* Sheep |
| Grant Support | |
ID/Acronym/Agency:
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HL073737/HL/NHLBI NIH HHS; HL097623/HL/NHLBI NIH HHS; R01 HL073737/HL/NHLBI NIH HHS; R01 HL073737-04/HL/NHLBI NIH HHS; R01 HL097623/HL/NHLBI NIH HHS; R01 HL097623-03/HL/NHLBI NIH HHS |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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