147 related articles for article (PubMed ID: 3130302)
1. The tyrosinase-positive oculocutaneous albinism locus is not linked to the beta-globin locus in man.
Heim RA; Dunn DS; Candy SE; Zwane E; Kromberg JG; Jenkins T
Hum Genet; 1988 May; 79(1):89. PubMed ID: 3130302
[TBL] [Abstract][Full Text] [Related]
2. A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinism.
Giebel LB; Strunk KM; King RA; Hanifin JM; Spritz RA
Proc Natl Acad Sci U S A; 1990 May; 87(9):3255-8. PubMed ID: 1970634
[TBL] [Abstract][Full Text] [Related]
3. Visual evoked potentials in Negro carriers of the gene for tyrosinase positive oculocutaneous albinism.
Castle D; Kromberg J; Kowalsky R; Moosa R; Gillman N; Zwane E; Fritz V
J Med Genet; 1988 Dec; 25(12):835-7. PubMed ID: 3148727
[TBL] [Abstract][Full Text] [Related]
4. Human oculocutaneous albinism caused by single base insertion in the tyrosinase gene.
Tomita Y; Takeda A; Okinaga S; Tagami H; Shibahara S
Biochem Biophys Res Commun; 1989 Nov; 164(3):990-6. PubMed ID: 2511845
[TBL] [Abstract][Full Text] [Related]
5. Allelism in human oculocutaneous albinism.
Warren ST
Am J Hum Genet; 1981 May; 33(3):479-80. PubMed ID: 6787918
[No Abstract] [Full Text] [Related]
6. A study of murine albinism using tyrosinase cDNA.
Shibahara S
Prog Clin Biol Res; 1988; 256():263-71. PubMed ID: 3130638
[No Abstract] [Full Text] [Related]
7. Hairbulb tyrosinase activity in oculocutaneous albinism: suggestions for pathway control and block location.
King RA; Olds DP
Am J Med Genet; 1985 Jan; 20(1):49-55. PubMed ID: 3918447
[TBL] [Abstract][Full Text] [Related]
8. Molecular analysis of the DNA segments cross-hybridizable to the tyrosinase gene in patients affected with oculocutaneous albinism.
Takeda A; Matsunaga J; Tomita Y; Tagami H; Shibahara S
Tohoku J Exp Med; 1989 Dec; 159(4):333-40. PubMed ID: 2517365
[TBL] [Abstract][Full Text] [Related]
9. Expression of tyrosinase gene in amelanotic mutant mice.
Takeuchi S; Yamamoto H; Takeuchi T
Biochem Biophys Res Commun; 1988 Aug; 155(1):470-5. PubMed ID: 3137937
[TBL] [Abstract][Full Text] [Related]
10. Exclusion of two candidate pigment loci, c and b, part of chromosome 11p, and 33 random polymorphic markers as the locus for tyrosinase-positive oculocutaneous albinism.
Colman MA; Stevens G; Ramsay M; Kwon B; Jenkins T
Hum Genet; 1993 Jan; 90(5):556-60. PubMed ID: 8428754
[TBL] [Abstract][Full Text] [Related]
11. Rescue of the albino phenotype by introduction of a functional tyrosinase gene into mice.
Beermann F; Ruppert S; Hummler E; Bosch FX; Müller G; Rüther U; Schütz G
EMBO J; 1990 Sep; 9(9):2819-26. PubMed ID: 2118105
[TBL] [Abstract][Full Text] [Related]
12. Comparative genetics of albinism.
Searle AG
Ophthalmic Paediatr Genet; 1990 Sep; 11(3):159-64. PubMed ID: 2126367
[TBL] [Abstract][Full Text] [Related]
13. Characteristic sequences in the upstream region of the human tyrosinase gene.
Kikuchi H; Miura H; Yamamoto H; Takeuchi T; Dei T; Watanabe M
Biochim Biophys Acta; 1989 Dec; 1009(3):283-6. PubMed ID: 2480811
[TBL] [Abstract][Full Text] [Related]
14. [Mouse model of tyrosinase positive type oculocutaneous albinism (chinchilla mouse, Cch/Cch) : tyrosinase activity and ultrastructure of hair bulb melanocyte (author's transl)].
Hori Y; Shichiro M; Mizoguchi M
Nihon Hifuka Gakkai Zasshi; 1980 Oct; 90(11):987-94. PubMed ID: 6780712
[No Abstract] [Full Text] [Related]
15. A Tyrosinase missense mutation causes albinism in the Wistar rat.
Blaszczyk WM; Arning L; Hoffmann KP; Epplen JT
Pigment Cell Res; 2005 Apr; 18(2):144-5. PubMed ID: 15760344
[TBL] [Abstract][Full Text] [Related]
16. Isolation, chromosomal mapping, and expression of the mouse tyrosinase gene.
Kwon BS; Haq AK; Wakulchik M; Kestler D; Barton DE; Francke U; Lamoreux ML; Whitney JB; Halaban R
J Invest Dermatol; 1989 Nov; 93(5):589-94. PubMed ID: 2507645
[TBL] [Abstract][Full Text] [Related]
17. The tyrosinase-positive oculocutaneous albinism locus maps to chromosome 15q11.2-q12.
Ramsay M; Colman MA; Stevens G; Zwane E; Kromberg J; Farrall M; Jenkins T
Am J Hum Genet; 1992 Oct; 51(4):879-84. PubMed ID: 1415228
[TBL] [Abstract][Full Text] [Related]
18. Detection of point mutation in the tyrosinase gene of a Japanese albino patient by a direct sequencing of amplified DNA.
Kikuchi H; Hara S; Ishiguro S; Tamai M; Watanabe M
Hum Genet; 1990 Jun; 85(1):123-4. PubMed ID: 2113511
[TBL] [Abstract][Full Text] [Related]
19. Murine and human b locus pigmentation genes encode a glycoprotein (gp75) with catalase activity.
Halaban R; Moellmann G
Proc Natl Acad Sci U S A; 1990 Jun; 87(12):4809-13. PubMed ID: 1693779
[TBL] [Abstract][Full Text] [Related]
20. Characterization of human hairbulb tyrosinase: properties of normal and albino enzyme.
King RA; Olds DP; Witkop CJ
J Invest Dermatol; 1978 Aug; 71(2):136-9. PubMed ID: 28370
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
