Woo SL - Search Results

1

Molecular basis of phenylketonuria and its clinical applications.

DiLella AG, Woo SL. DiLella AG, et al. Among authors: woo sl. Mol Biol Med. 1987 Aug;4(4):183-92. Mol Biol Med. 1987. PMID: 2890077 Review. No abstract available.

2

Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuria.

Lidsky AS, Ledley FD, DiLella AG, Kwok SC, Daiger SP, Robson KJ, Woo SL. Lidsky AS, et al. Among authors: woo sl. Am J Hum Genet. 1985 Jul;37(4):619-34. Am J Hum Genet. 1985. PMID: 9556654 Free PMC article.

3

Molecular basis of phenylketonuria and potential somatic gene therapy.

Woo SL, DiLella AG, Marvit J, Ledley FD. Woo SL, et al. Cold Spring Harb Symp Quant Biol. 1986;51 Pt 1:395-401. doi: 10.1101/sqb.1986.051.01.047. Cold Spring Harb Symp Quant Biol. 1986. PMID: 2884065 No abstract available.

4

Molecular biology of phenylketonuria.

Güttler F, DiLella AG, Ledley FD, Lidsky AS, Kvok SC, Marvit J, Woo SL. Güttler F, et al. Among authors: woo sl. Eur J Pediatr. 1987;146 Suppl 1:A5-11. doi: 10.1007/BF00442048. Eur J Pediatr. 1987. PMID: 2891509 No abstract available.

5

Screening for phenylketonuria mutations by DNA amplification with the polymerase chain reaction.

DiLella AG, Huang WM, Woo SL. DiLella AG, et al. Among authors: woo sl. Lancet. 1988 Mar 5;1(8584):497-9. doi: 10.1016/s0140-6736(88)91295-0. Lancet. 1988. PMID: 2893918

6

Molecular basis of phenylketonuria and recombinant DNA strategies for its therapy.

Woo SL, DiLella AG, Marvit J, Ledley FD. Woo SL, et al. Enzyme. 1987;38(1-4):207-13. doi: 10.1159/000469206. Enzyme. 1987. PMID: 2894302

7

Detection of phenylalanine hydroxylase messenger RNA in liver biopsy samples from patients with phenylketonuria.

DiLella AG, Ledley FD, Rey F, Munnich A, Woo SL. DiLella AG, et al. Among authors: woo sl. Lancet. 1985 Jan 19;1(8421):160-1. doi: 10.1016/s0140-6736(85)91925-7. Lancet. 1985. PMID: 2857230 No abstract available.

8

Correlation between polymorphic DNA haplotypes at phenylalanine hydroxylase locus and clinical phenotypes of phenylketonuria.

Güttler F, Ledley FD, Lidsky AS, DiLella AG, Sullivan SE, Woo SL. Güttler F, et al. Among authors: woo sl. J Pediatr. 1987 Jan;110(1):68-71. doi: 10.1016/s0022-3476(87)80290-1. J Pediatr. 1987. PMID: 2878985

9

Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria.

Chakraborty R, Lidsky AS, Daiger SP, Güttler F, Sullivan S, Dilella AG, Woo SL. Chakraborty R, et al. Among authors: woo sl. Hum Genet. 1987 May;76(1):40-6. doi: 10.1007/BF00283048. Hum Genet. 1987. PMID: 2883110

10

An amino-acid substitution involved in phenylketonuria is in linkage disequilibrium with DNA haplotype 2.

DiLella AG, Marvit J, Brayton K, Woo SL. DiLella AG, et al. Among authors: woo sl. Nature. 1987 May 28-Jun 3;327(6120):333-6. doi: 10.1038/327333a0. Nature. 1987. PMID: 2884570

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