These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
139 related articles for article (PubMed ID: 1312261)
1. Reconstitution of enzymatic activity in hepatocytes of phenylalanine hydroxylase-deficient mice. Liu TJ; Kay MA; Darlington GJ; Woo SL Somat Cell Mol Genet; 1992 Jan; 18(1):89-96. PubMed ID: 1312261 [TBL] [Abstract][Full Text] [Related]
2. Retroviral-mediated gene transfer of human phenylalanine hydroxylase into NIH 3T3 and hepatoma cells. Ledley FD; Grenett HE; McGinnis-Shelnutt M; Woo SL Proc Natl Acad Sci U S A; 1986 Jan; 83(2):409-13. PubMed ID: 3455778 [TBL] [Abstract][Full Text] [Related]
3. Long-term enzymatic and phenotypic correction in the phenylketonuria mouse model by adeno-associated virus vector-mediated gene transfer. Oh HJ; Park ES; Kang S; Jo I; Jung SC Pediatr Res; 2004 Aug; 56(2):278-84. PubMed ID: 15181195 [TBL] [Abstract][Full Text] [Related]
4. Expression of human phenylalanine hydroxylase activity in T lymphocytes of classical phenylketonuria children by retroviral-mediated gene transfer. Lin CM; Tan Y; Lee YM; Chang CC; Hsiao KJ J Inherit Metab Dis; 1997 Nov; 20(6):742-54. PubMed ID: 9427141 [TBL] [Abstract][Full Text] [Related]
5. Hepatocytes from wild-type or heterozygous donors are equally effective in achieving successful therapeutic liver repopulation in murine phenylketonuria (PKU). Hamman KJ; Winn SR; Harding CO Mol Genet Metab; 2011 Nov; 104(3):235-40. PubMed ID: 21917493 [TBL] [Abstract][Full Text] [Related]
6. Gene therapy for phenylketonuria: phenotypic correction in a genetically deficient mouse model by adenovirus-mediated hepatic gene transfer. Fang B; Eisensmith RC; Li XH; Finegold MJ; Shedlovsky A; Dove W; Woo SL Gene Ther; 1994 Jul; 1(4):247-54. PubMed ID: 7584088 [TBL] [Abstract][Full Text] [Related]