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Results: 1 to 20 of 222

1.

Tyrosinase mutations associated with Siamese and Burmese patterns in the domestic cat (Felis catus).

Lyons LA, Imes DL, Rah HC, Grahn RA.

Anim Genet. 2005 Apr;36(2):119-26.

PMID:
15771720
[PubMed - indexed for MEDLINE]
2.

Albinism in the domestic cat (Felis catus) is associated with a tyrosinase (TYR) mutation.

Imes DL, Geary LA, Grahn RA, Lyons LA.

Anim Genet. 2006 Apr;37(2):175-8.

PMID:
16573534
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Tyrosinase and tyrosinase related protein 1 alleles specify domestic cat coat color phenotypes of the albino and brown loci.

Schmidt-Küntzel A, Eizirik E, O'Brien SJ, Menotti-Raymond M.

J Hered. 2005 Jul-Aug;96(4):289-301. Epub 2005 Apr 27.

PMID:
15858157
[PubMed - indexed for MEDLINE]
Free Article
4.

Chocolate coated cats: TYRP1 mutations for brown color in domestic cats.

Lyons LA, Foe IT, Rah HC, Grahn RA.

Mamm Genome. 2005 May;16(5):356-66.

PMID:
16104383
[PubMed - indexed for MEDLINE]
5.

A tyrosinase gene missense mutation in temperature-sensitive type I oculocutaneous albinism. A human homologue to the Siamese cat and the Himalayan mouse.

Giebel LB, Tripathi RK, King RA, Spritz RA.

J Clin Invest. 1991 Mar;87(3):1119-22.

PMID:
1900309
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Molecular characterization of the Himalayan mink.

Benkel BF, Rouvinen-Watt K, Farid H, Anistoroaei R.

Mamm Genome. 2009 Apr;20(4):256-9. doi: 10.1007/s00335-009-9177-6. Epub 2009 Mar 24.

PMID:
19308642
[PubMed - indexed for MEDLINE]
7.

Mutation analysis of the tyrosinase gene in oculocutaneous albinism.

Camand O, Marchant D, Boutboul S, Péquignot M, Odent S, Dollfus H, Sutherland J, Levin A, Menasche M, Marsac C, Dufier JL, Heon E, Abitbol M.

Hum Mutat. 2001 Apr;17(4):352.

PMID:
11295837
[PubMed - indexed for MEDLINE]
8.

Feline polycystic kidney disease mutation identified in PKD1.

Lyons LA, Biller DS, Erdman CA, Lipinski MJ, Young AE, Roe BA, Qin B, Grahn RA.

J Am Soc Nephrol. 2004 Oct;15(10):2548-55.

PMID:
15466259
[PubMed - indexed for MEDLINE]
Free Article
9.

A homozygous single-base deletion in MLPH causes the dilute coat color phenotype in the domestic cat.

Ishida Y, David VA, Eizirik E, Schäffer AA, Neelam BA, Roelke ME, Hannah SS, O'brien SJ, Menotti-Raymond M.

Genomics. 2006 Dec;88(6):698-705. Epub 2006 Jul 24.

PMID:
16860533
[PubMed - indexed for MEDLINE]
Free Article
10.

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.

PMID:
15760344
[PubMed - indexed for MEDLINE]
11.

Missense and nonsense mutations in melanocortin 1 receptor (MC1R) gene of different goat breeds: association with red and black coat colour phenotypes but with unexpected evidences.

Fontanesi L, Beretti F, Riggio V, Dall'Olio S, González EG, Finocchiaro R, Davoli R, Russo V, Portolano B.

BMC Genet. 2009 Aug 25;10:47. doi: 10.1186/1471-2156-10-47.

PMID:
19706191
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Identification of a tyrosinase (TYR) exon 4 deletion in albino ferrets (Mustela putorius furo).

Blaszczyk WM, Distler C, Dekomien G, Arning L, Hoffmann KP, Epplen JT.

Anim Genet. 2007 Aug;38(4):421-3.

PMID:
17655555
[PubMed - indexed for MEDLINE]
13.

Albinism in the American mink (Neovison vison) is associated with a tyrosinase nonsense mutation.

Anistoroaei R, Fredholm M, Christensen K, Leeb T.

Anim Genet. 2008 Dec;39(6):645-8. doi: 10.1111/j.1365-2052.2008.01788.x. Epub 2008 Sep 24.

PMID:
18822100
[PubMed - indexed for MEDLINE]
14.

A missense mutation in PMEL17 is associated with the Silver coat color in the horse.

Brunberg E, Andersson L, Cothran G, Sandberg K, Mikko S, Lindgren G.

BMC Genet. 2006 Oct 9;7:46.

PMID:
17029645
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Prevalent and novel mutations of the tyrosinase gene in Korean patients with tyrosinase-deficient oculocutaneous albinism.

Park SK, Lee KH, Park KC, Lee JS, Spritz RA, Lee ST.

Mol Cells. 1997 Apr 30;7(2):187-91.

PMID:
9163730
[PubMed - indexed for MEDLINE]
Free Article
16.

Molecular basis of mouse Himalayan mutation.

Kwon BS, Halaban R, Chintamaneni C.

Biochem Biophys Res Commun. 1989 May 30;161(1):252-60.

PMID:
2567165
[PubMed - indexed for MEDLINE]
17.

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.

PMID:
1970634
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Somatic mutations of the thyroid-stimulating hormone receptor gene in feline hyperthyroidism: parallels with human hyperthyroidism.

Watson SG, Radford AD, Kipar A, Ibarrola P, Blackwood L.

J Endocrinol. 2005 Sep;186(3):523-37.

PMID:
16135672
[PubMed - indexed for MEDLINE]
Free Article
19.

Melanocortin 1-receptor (MC1R) mutations are associated with plumage colour in chicken.

Kerje S, Lind J, Schütz K, Jensen P, Andersson L.

Anim Genet. 2003 Aug;34(4):241-8.

PMID:
12873211
[PubMed - indexed for MEDLINE]
20.

A novel mutation of the tyrosinase gene causing oculocutaneous albinism type 1 (OCA1).

Nakamura E, Miyamura Y, Matsunaga J, Kano Y, Dakeishi-Hara M, Tanita M, Kono M, Tomita Y.

J Dermatol Sci. 2002 Feb;28(2):102-5.

PMID:
11858948
[PubMed - indexed for MEDLINE]

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