Mouse hepatocytes migrate to liver parenchyma and function indefinitely after intrasplenic transplantation.

One approach to gene therapy for hepatic diseases is to remove hepatocytes from an affected individual, genetically alter them in vitro, and reimplant them into a receptive locus. Although returning hepatocytes to the liver itself would be advantageous, the feasibility of this approach has never bee...

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Библиографические подробности
Главные авторы: Ponder, K P, Gupta, S, Leland, F, Darlington, G, Finegold, M, DeMayo, J, Ledley, F D, Chowdhury, J R, Woo, S L
Формат: Artigo
Язык:Inglês
Опубликовано: 1991
Предметы:
Research Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC50988/
https://ncbi.nlm.nih.gov/pubmed/1899924
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