Expression of human alpha 1-antitrypsin in dogs after autologous transplantation of retroviral transduced hepatocytes.

The liver represents an excellent organ for gene therapy since many genetic disorders result from the deficiency of liver-specific gene products. We have previously demonstrated that transgenic mouse hepatocytes can be heterologously transplanted into congenic recipients where they survived indefini...

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Detalhes bibliográficos

Publicado no:	Proc Natl Acad Sci U S A
Principais autores:	Kay, M A, Baley, P, Rothenberg, S, Leland, F, Fleming, L, Ponder, K P, Liu, T, Finegold, M, Darlington, G, Pokorny, W
Formato:	Artigo
Idioma:	Inglês
Publicado em:	National Academy of Sciences 1992
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC48181/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1729724/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.89.1.89
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