King RA - Search Results

1

Molecular basis of type IA (tyrosinase negative) oculocutaneous albinism.

King RA, Oetting WS. King RA, et al. Pigment Cell Res. 1992;Suppl 2:249-53. doi: 10.1111/j.1600-0749.1990.tb00380.x. Pigment Cell Res. 1992. PMID: 1409426

2

Identification and characterization of a DNase hypersensitive region of the human tyrosinase gene.

Fryer JP, Oetting WS, King RA. Fryer JP, et al. Among authors: king ra. Pigment Cell Res. 2003 Dec;16(6):679-84. doi: 10.1046/j.1600-0749.2003.00099.x. Pigment Cell Res. 2003. PMID: 14629726

3

P gene mutations associated with oculocutaneous albinism type II (OCA2).

Oetting WS, Garrett SS, Brott M, King RA. Oetting WS, et al. Among authors: king ra. Hum Mutat. 2005 Mar;25(3):323. doi: 10.1002/humu.9318. Hum Mutat. 2005. PMID: 15712365

4

The R402Q tyrosinase variant does not cause autosomal recessive ocular albinism.

Oetting WS, Pietsch J, Brott MJ, Savage S, Fryer JP, Summers CG, King RA. Oetting WS, et al. Among authors: king ra. Am J Med Genet A. 2009 Mar;149A(3):466-9. doi: 10.1002/ajmg.a.32654. Am J Med Genet A. 2009. PMID: 19208379

5

Tyrosinase gene mutations in oculocutaneous albinism 1 (OCA1): definition of the phenotype.

King RA, Pietsch J, Fryer JP, Savage S, Brott MJ, Russell-Eggitt I, Summers CG, Oetting WS. King RA, et al. Hum Genet. 2003 Nov;113(6):502-13. doi: 10.1007/s00439-003-0998-1. Epub 2003 Sep 10. Hum Genet. 2003. PMID: 13680365

6

MC1R mutations modify the classic phenotype of oculocutaneous albinism type 2 (OCA2).

King RA, Willaert RK, Schmidt RM, Pietsch J, Savage S, Brott MJ, Fryer JP, Summers CG, Oetting WS. King RA, et al. Am J Hum Genet. 2003 Sep;73(3):638-45. doi: 10.1086/377569. Epub 2003 Jul 22. Am J Hum Genet. 2003. PMID: 12876664 Free PMC article.

7

Oculocutaneous albinism type 1: the last 100 years.

Oetting WS, Fryer JP, Shriram S, King RA. Oetting WS, et al. Among authors: king ra. Pigment Cell Res. 2003 Jun;16(3):307-11. doi: 10.1034/j.1600-0749.2003.00045.x. Pigment Cell Res. 2003. PMID: 12753405 Review.

8

Molecular analysis of type I-A (tyrosinase negative) oculocutaneous albinism.

Oetting WS, King RA. Oetting WS, et al. Among authors: king ra. Hum Genet. 1992 Nov;90(3):258-62. doi: 10.1007/BF00220074. Hum Genet. 1992. PMID: 1487241

9

Molecular analysis of an extended family with type IA (tyrosinase-negative) oculocutaneous albinism.

Oetting WS, Handoko HY, Mentink MM, Paller AS, White JG, King RA. Oetting WS, et al. Among authors: king ra. J Invest Dermatol. 1991 Jul;97(1):15-9. doi: 10.1111/1523-1747.ep12477808. J Invest Dermatol. 1991. PMID: 1676041 Free article.

10

PCR detection of a TaqI polymorphism at the CCAATT box of the human tyrosinase (TYR) gene.

Oetting WS, Roed CM, Mentink MM, King RA. Oetting WS, et al. Among authors: king ra. Nucleic Acids Res. 1991 Oct 25;19(20):5800. doi: 10.1093/nar/19.20.5800-a. Nucleic Acids Res. 1991. PMID: 1682887 Free PMC article. No abstract available.

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