Retroviral-mediated gene transfer of human phenylalanine hydroxylase into NIH 3T3 and hepatoma cells.

Phenylketonuria (PKU) is caused by deficiency of the hepatic enzyme phenylalanine hydroxylase (PAH). A full-length human PAH cDNA sequence has been inserted into pzip-neoSV(X), which is a retroviral vector containing the bacterial neo gene. The recombinant has been transfected into psi 2 cells, whic...

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Dades bibliogràfiques

Publicat a:	Proc Natl Acad Sci U S A
Autors principals:	Ledley, F D, Grenett, H E, McGinnis-Shelnutt, M, Woo, S L
Format:	Artigo
Idioma:	Inglês
Publicat:	National Academy of Sciences 1986
Matèries:	Research Article
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC322868/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3455778/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.83.2.409
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