Ledley FD - Search Results

1

Physical and genetic localization of quinonoid dihydropteridine reductase gene (QDPR) on short arm of chromosome 4.

MacDonald ME, Anderson MA, Lockyer JL, Milstien S, Hobbs WJ, Faryniarz AG, Kaufman S, Ledley FD, Woo SL, Gusella JF. MacDonald ME, et al. Among authors: ledley fd. Somat Cell Mol Genet. 1987 Sep;13(5):569-74. doi: 10.1007/BF01534498. Somat Cell Mol Genet. 1987. PMID: 2889272

2

Synteny on mouse chromosome 5 of homologs for human DNA loci linked to the Huntington disease gene.

Cheng SV, Martin GR, Nadeau JH, Haines JL, Bucan M, Kozak CA, MacDonald ME, Lockyer JL, Ledley FD, Woo SL, et al. Cheng SV, et al. Among authors: ledley fd. Genomics. 1989 Apr;4(3):419-26. doi: 10.1016/0888-7543(89)90349-2. Genomics. 1989. PMID: 2523855

3

Assignment of human tryptophan hydroxylase locus to chromosome 11: gene duplication and translocation in evolution of aromatic amino acid hydroxylases.

Ledley FD, Grenett HE, Bartos DP, van Tuinen P, Ledbetter DH, Woo SL. Ledley FD, et al. Somat Cell Mol Genet. 1987 Sep;13(5):575-80. doi: 10.1007/BF01534499. Somat Cell Mol Genet. 1987. PMID: 2889273

4

Structure and expression of human dihydropteridine reductase.

Lockyer J, Cook RG, Milstien S, Kaufman S, Woo SL, Ledley FD. Lockyer J, et al. Among authors: ledley fd. Proc Natl Acad Sci U S A. 1987 May;84(10):3329-33. doi: 10.1073/pnas.84.10.3329. Proc Natl Acad Sci U S A. 1987. PMID: 3033643 Free PMC article.

5

Localization of mouse phenylalanine hydroxylase locus on chromosome 10.

Ledley FD, Ledbetter SA, Ledbetter DH, Woo SL. Ledley FD, et al. Cytogenet Cell Genet. 1988;47(3):125-6. doi: 10.1159/000132528. Cytogenet Cell Genet. 1988. PMID: 3378451

6

Selection for phenylalanine hydroxylase activity in cells transformed with recombinant retroviruses.

Ledley FD, Hahn T, Woo SL. Ledley FD, et al. Somat Cell Mol Genet. 1987 Mar;13(2):145-54. doi: 10.1007/BF01534694. Somat Cell Mol Genet. 1987. PMID: 3470952

7

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

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

8

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: ledley fd. Am J Hum Genet. 1985 Jul;37(4):619-34. Am J Hum Genet. 1985. PMID: 9556654 Free PMC article.

9

Molecular basis of phenylketonuria and potential somatic gene therapy.

Woo SL, DiLella AG, Marvit J, Ledley FD. Woo SL, et al. Among authors: ledley fd. 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.

10

Molecular structure and polymorphic map of the human phenylalanine hydroxylase gene.

DiLella AG, Kwok SC, Ledley FD, Marvit J, Woo SL. DiLella AG, et al. Among authors: ledley fd. Biochemistry. 1986 Feb 25;25(4):743-9. doi: 10.1021/bi00352a001. Biochemistry. 1986. PMID: 3008810

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