HD-17711/HD/NICHD NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1983	1
1984	4
1985	6
1986	5
1987	10
1988	5
1989	5
1990	6
1991	10
1992	9
1993	3
1994	3
1995	1
1996	1
1999	1
2024	0

1

Molecular basis and population genetics of phenylketonuria.

Woo SL. Woo SL. Biochemistry. 1989 Jan 10;28(1):1-7. doi: 10.1021/bi00427a001. Biochemistry. 1989. PMID: 2565120 Review. No abstract available.

2

Phenylketonuria and the phenylalanine hydroxylase gene.

Eisensmith RC, Woo SL. Eisensmith RC, et al. Mol Biol Med. 1991 Feb;8(1):3-18. Mol Biol Med. 1991. PMID: 1943687 Review.

3

Molecular basis of phenylketonuria and related hyperphenylalaninemias: mutations and polymorphisms in the human phenylalanine hydroxylase gene.

Eisensmith RC, Woo SL. Eisensmith RC, et al. Hum Mutat. 1992;1(1):13-23. doi: 10.1002/humu.1380010104. Hum Mutat. 1992. PMID: 1301187 Review.

4

Molecular genetic analysis of phenylketonuria and mental retardation.

Woo SL. Woo SL. Res Publ Assoc Res Nerv Ment Dis. 1991;69:193-203. Res Publ Assoc Res Nerv Ment Dis. 1991. PMID: 1672237 Review. No abstract available.

5

Gene transfer and expression of human phenylalanine hydroxylase.

Ledley FD, Grenett HE, DiLella AG, Kwok SC, Woo SL. Ledley FD, et al. Science. 1985 Apr 5;228(4695):77-9. doi: 10.1126/science.3856322. Science. 1985. PMID: 3856322

6

Structural characterization of the 5' regions of the human phenylalanine hydroxylase gene.

Konecki DS, Wang Y, Trefz FK, Lichter-Konecki U, Woo SL. Konecki DS, et al. Biochemistry. 1992 Sep 8;31(35):8363-8. doi: 10.1021/bi00150a033. Biochemistry. 1992. PMID: 1326329

7

Haplotype distribution of the human phenylalanine hydroxylase locus in Scotland and Switzerland.

Sullivan SE, Moore SD, Connor JM, King M, Cockburn F, Steinmann B, Gitzelmann R, Daiger SP, Woo SL. Sullivan SE, et al. Am J Hum Genet. 1989 May;44(5):652-9. Am J Hum Genet. 1989. PMID: 2565077 Free PMC article.

8

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

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

9

Phenylketonuria missense mutations in the Mediterranean.

Okano Y, Wang T, Eisensmith RC, Longhi R, Riva E, Giovannini M, Cerone R, Romano C, Woo SL. Okano Y, et al. Genomics. 1991 Jan;9(1):96-103. doi: 10.1016/0888-7543(91)90225-4. Genomics. 1991. PMID: 1672294

10

The PKU locus in man is on chromosome 12.

Lidksy AS, Robson KJ, Thirumalachary C, Barker PE, Ruddle FH, Woo SL. Lidksy AS, et al. Am J Hum Genet. 1984 May;36(3):527-33. Am J Hum Genet. 1984. PMID: 6547271 Free PMC article.

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