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Items: 1 to 20 of 25

1.

Evidence for genetic admixture as a determinant in the occurrence of insulin-dependent diabetes mellitus in U.S. blacks.

Reitnauer PJ, Go RC, Acton RT, Murphy CC, Budowle B, Barger BO, Roseman JM.

Diabetes. 1982 Jun;31(6 Pt 1):532-7.

PMID:
7152138
2.

The PKU locus in man is on chromosome 12.

Lidksy AS, Robson KJ, Thirumalachary C, Barker PE, Ruddle FH, Woo SL.

Am J Hum Genet. 1984 May;36(3):527-33.

3.

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.

Feinberg AP, Vogelstein B.

Anal Biochem. 1983 Jul 1;132(1):6-13.

PMID:
6312838
4.

The isolation and properties of phenylalanine hydroxylase from human liver.

Woo SL, Gillam SS, Woolf LI.

Biochem J. 1974 Jun;139(3):741-9.

5.

Characterization of beta-thalassaemia mutations using direct genomic sequencing of amplified single copy DNA.

Wong C, Dowling CE, Saiki RK, Higuchi RG, Erlich HA, Kazazian HH Jr.

Nature. 1987 Nov 26-Dec 2;330(6146):384-6.

PMID:
3683554
6.

Full-length cDNA for rabbit tryptophan hydroxylase: functional domains and evolution of aromatic amino acid hydroxylases.

Grenett HE, Ledley FD, Reed LL, Woo SL.

Proc Natl Acad Sci U S A. 1987 Aug;84(16):5530-4.

7.

Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction.

Mullis KB, Faloona FA.

Methods Enzymol. 1987;155:335-50. No abstract available.

PMID:
3431465
8.

Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuria.

DiLella AG, Marvit J, Lidsky AS, Güttler F, Woo SL.

Nature. 1986 Aug 28-Sep 3;322(6082):799-803.

PMID:
3018584
9.

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

DiLella AG, Kwok SC, Ledley FD, Marvit J, Woo SL.

Biochemistry. 1986 Feb 25;25(4):743-9.

PMID:
3008810
10.

Nucleotide sequence of a full-length complementary DNA clone and amino acid sequence of human phenylalanine hydroxylase.

Kwok SC, Ledley FD, DiLella AG, Robson KJ, Woo SL.

Biochemistry. 1985 Jan 29;24(3):556-61.

PMID:
2986678
11.

Collation of RFLP haplotypes at the human phenylalanine hydroxylase (PAH) locus.

Woo SL.

Am J Hum Genet. 1988 Nov;43(5):781-3. No abstract available.

12.

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

DiLella AG, Marvit J, Brayton K, Woo SL.

Nature. 1987 May 28-Jun 3;327(6120):333-6.

PMID:
2884570
13.
14.

Phenylketonuria in the Greek population. Haplotype analysis of the phenylalanine hydroxylase gene and identification of a PKU mutation.

Hofman KJ, Antonarakis SE, Missiou-Tsangaraki S, Boehm CD, Valle D.

Mol Biol Med. 1989 Jun;6(3):245-50.

PMID:
2615649
15.

Phenylketonuria: detection of a frequent haplotype 4 allele mutation.

Dworniczak B, Aulehla-Scholz C, Horst J.

Hum Genet. 1989 Dec;84(1):95-6.

PMID:
2606484
16.

CpG dinucleotides are mutation hot spots in phenylketonuria.

Abadie V, Lyonnet S, Maurin N, Berthelon M, Caillaud C, Giraud F, Mattei JF, Rey J, Rey F, Munnich A.

Genomics. 1989 Nov;5(4):936-9.

PMID:
2574153
17.

Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in Asian families with phenylketonuria (PKU).

Daiger SP, Reed L, Huang SS, Zeng YT, Wang T, Lo WH, Okano Y, Hase Y, Fukuda Y, Oura T, et al.

Am J Hum Genet. 1989 Aug;45(2):319-24.

18.

Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in European families with phenylketonuria (PKU).

Daiger SP, Chakraborty R, Reed L, Fekete G, Schuler D, Berenssi G, Nasz I, Brdicka R, Kamarýt J, Pijácková A, et al.

Am J Hum Genet. 1989 Aug;45(2):310-8.

19.

Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiency.

Lyonnet S, Caillaud C, Rey F, Berthelon M, Frézal J, Rey J, Munnich A.

Am J Hum Genet. 1989 Apr;44(4):511-7.

20.

Phenylalanine hydroxylase gene haplotypes in Polynesians: evolutionary origins and absence of alleles associated with severe phenylketonuria.

Hertzberg M, Jahromi K, Ferguson V, Dahl HH, Mercer J, Mickleson KN, Trent RJ.

Am J Hum Genet. 1989 Mar;44(3):382-7.

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