Woo SL - Search Results

1

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. Fang B, et al. Among authors: woo sl. Gene Ther. 1994 Jul;1(4):247-54. Gene Ther. 1994. PMID: 7584088

2

Gene therapy in heart disease.

Smith LC, Eisensmith RC, Woo SL. Smith LC, et al. Among authors: woo sl. Adv Exp Med Biol. 1995;369:79-88. doi: 10.1007/978-1-4615-1957-7_8. Adv Exp Med Biol. 1995. PMID: 7598019 Review.

3

Molecular genetics of phenylketonuria: from molecular anthropology to gene therapy.

Eisensmith RC, Woo SL. Eisensmith RC, et al. Among authors: woo sl. Adv Genet. 1995;32:199-271. doi: 10.1016/s0065-2660(08)60206-0. Adv Genet. 1995. PMID: 7741023 Review. No abstract available.

4

Gene therapy for phenylketonuria.

Eisensmith RC, Woo SL. Eisensmith RC, et al. Among authors: woo sl. Acta Paediatr Suppl. 1994 Dec;407:124-9. doi: 10.1111/j.1651-2227.1994.tb13471.x. Acta Paediatr Suppl. 1994. PMID: 7766948 Review.

5

Population genetics of phenylketonuria.

Eisensmith RC, Woo SL. Eisensmith RC, et al. Among authors: woo sl. Acta Paediatr Suppl. 1994 Dec;407:19-26. doi: 10.1111/j.1651-2227.1994.tb13442.x. Acta Paediatr Suppl. 1994. PMID: 7766949 Review.

6

A simple, rapid, and highly informative PCR-based procedure for prenatal diagnosis and carrier screening of phenylketonuria.

Eisensmith RC, Goltsov AA, Woo SL. Eisensmith RC, et al. Among authors: woo sl. Prenat Diagn. 1994 Dec;14(12):1113-8. doi: 10.1002/pd.1970141204. Prenat Diagn. 1994. PMID: 7899279

7

Hepatic gene therapy: efficient retroviral-mediated gene transfer into rat hepatocytes in vivo.

Kolodka TM, Finegold M, Kay MA, Woo SL. Kolodka TM, et al. Among authors: woo sl. Somat Cell Mol Genet. 1993 Sep;19(5):491-7. doi: 10.1007/BF01233254. Somat Cell Mol Genet. 1993. PMID: 7980740

8

Three polymorphisms but no disease-causing mutations in the proximal part of the promoter of the phenylalanine hydroxylase gene.

Svensson E, Wang Y, Eisensmith RC, Hagenfeldt L, Woo SL. Svensson E, et al. Among authors: woo sl. Eur J Hum Genet. 1993;1(4):306-13. doi: 10.1159/000472429. Eur J Hum Genet. 1993. PMID: 8081944

9

A single polymorphic STR system in the human phenylalanine hydroxylase gene permits rapid prenatal diagnosis and carrier screening for phenylketonuria.

Goltsov AA, Eisensmith RC, Naughton ER, Jin L, Chakraborty R, Woo SL. Goltsov AA, et al. Among authors: woo sl. Hum Mol Genet. 1993 May;2(5):577-81. doi: 10.1093/hmg/2.5.577. Hum Mol Genet. 1993. PMID: 8100164

10

Assessment of recombinant adenoviral vectors for hepatic gene therapy.

Li Q, Kay MA, Finegold M, Stratford-Perricaudet LD, Woo SL. Li Q, et al. Among authors: woo sl. Hum Gene Ther. 1993 Aug;4(4):403-9. doi: 10.1089/hum.1993.4.4-403. Hum Gene Ther. 1993. PMID: 8399487

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