-
1
-
-
55949127974
-
Albinism in the American mink (Neovison vison) is associated with a tyrosinase nonsense mutation
-
Anistoroaei R, Fredholm M, Christensen K, Leeb T. 2008. Albinism in the American mink (Neovison vison) is associated with a tyrosinase nonsense mutation. Anim Genet. 39:645-648.
-
(2008)
Anim Genet
, vol.39
, pp. 645-648
-
-
Anistoroaei, R.1
Fredholm, M.2
Christensen, K.3
Leeb, T.4
-
2
-
-
18044402480
-
Mutation analysis of the tyrosinase gene in oculocutaneous albinism
-
Camand O, Marchant D, Boutboul S, Pequignot M, Odent S, Dollfus H, Sutherland J, Levin A, Menasche M, Marsac C, et al. 2001. Mutation analysis of the tyrosinase gene in oculocutaneous albinism. Hum Mutat. 17:352.
-
(2001)
Hum Mutat
, vol.17
, pp. 352
-
-
Camand, O.1
Marchant, D.2
Boutboul, S.3
Pequignot, M.4
Odent, S.5
Dollfus, H.6
Sutherland, J.7
Levin, A.8
Menasche, M.9
Marsac, C.10
-
3
-
-
55149105361
-
An update on anomalously white cetaceans, including the first account for the pantropical spotted dolphin (Stenella attenuata graffmani)
-
Fertl D, Barros NB, Rowlett RA, Estes S, Richlen M. 2004. An update on anomalously white cetaceans, including the first account for the pantropical spotted dolphin (Stenella attenuata graffmani). Lat Am J Aquat Mamm. 3:163-166.
-
(2004)
Lat Am J Aquat Mamm
, vol.3
, pp. 163-166
-
-
Fertl, D.1
Barros, N.B.2
Rowlett, R.A.3
Estes, S.4
Richlen, M.5
-
4
-
-
0035744609
-
Observations of a hypo-pigmented humpback whale, Megaptera novaeangliae, off east coast Australia: 1991-2000
-
Forestell PH, Paton DA, Hodda P, Kaufman GD. 2001. Observations of a hypo-pigmented humpback whale (Megaptera novaeangliae) off east-coast Australia: 1991-2000. Mem Queensl Mus. 47(2):437-450. (Pubitemid 34735775)
-
(2001)
Memoirs of the Queensland Museum
, vol.47
, Issue.2
, pp. 437-450
-
-
Forestell, P.H.1
Paton, D.A.2
Hodda, P.3
Kaufman, G.D.4
-
5
-
-
0025868437
-
A nonsense mutation in the tyrosinase gene of Afghan patients with tyrosinase negative (type IA) oculocutaneous albinism
-
Giebel LB, Musarella MA, Spritz RA. 1991. A nonsense mutation in the tyrosinase gene of Afghan patients with tyrosinase negative (type IA) oculocutaneous albinism. J Med Genet. 28:464-467. (Pubitemid 21922640)
-
(1991)
Journal of Medical Genetics
, vol.28
, Issue.7
, pp. 464-467
-
-
Giebel, L.B.1
Musarella, M.A.2
Spritz, R.A.3
-
7
-
-
33645210498
-
Albinism in the domestic cat (Felis catus) is associated with a tyrosinase (TYR) mutation
-
Imes DL, Geary LA, Grahn RA, Lyons LA. 2006. Albinism in the domestic cat (Felis catus) is associated with a tyrosinase (TYR) mutation. Anim Genet. 37:175-178.
-
(2006)
Anim Genet
, vol.37
, pp. 175-178
-
-
Imes, D.L.1
Geary, L.A.2
Grahn, R.A.3
Lyons, L.A.4
-
8
-
-
0002554067
-
Biochemistry of melanin formation
-
Lerner AB, Fitzpatrick TB. 1950. Biochemistry of melanin formation. Physiol Rev. 30:91-126.
-
(1950)
Physiol Rev
, vol.30
, pp. 91-126
-
-
Lerner, A.B.1
Fitzpatrick, T.B.2
-
9
-
-
79954456215
-
Acute sun damage and photoprotective responses in whales
-
Martinez-Levasseur LM, Gendron D, Knell RJ, O'Toole EA, Singh M, Acevedo-Whitehouse K. 2010. Acute sun damage and photoprotective responses in whales. Proc Biol Sci. 278:1581-1586.
-
(2010)
Proc Biol Sci
, vol.278
, pp. 1581-1586
-
-
Martinez-Levasseur, L.M.1
Gendron, D.2
Knell, R.J.3
O'toole, E.A.4
Singh, M.5
Acevedo-Whitehouse, K.6
-
10
-
-
0025788758
-
Three different frameshift mutations of the tyrosinase gene in type IA oculocutaneous albinism
-
Oetting WS, Mentink M, Summers CG, Lewis RA, White JG, King RA. 1991. Three different frameshift mutations of the tyrosinase gene in type IA oculocutaneous albinism. Am J Hum Genet. 49:199-206. (Pubitemid 21891668)
-
(1991)
American Journal of Human Genetics
, vol.49
, Issue.1
, pp. 199-206
-
-
Oetting, W.S.1
Mentink, M.M.2
Summers, C.G.3
Lewis, R.A.4
White, J.G.5
King, R.A.6
-
11
-
-
0027531665
-
Molecular basis of Type I (Tryrosinase-related) oculocutaneous albinism: Mutations and polymorphisms of the human tyrosinase gene
-
Oetting WS, King RA. 1993. Molecular basis of type 1 (tyrosinase-related) oculocutaneous albinism: mutations and polymorphisms of the human tyrosinase gene. Hum Mutat. 2:1-6. (Pubitemid 23104789)
-
(1993)
Human Mutation
, vol.2
, Issue.1
, pp. 1-6
-
-
Oetting, W.S.1
King, R.A.2
-
12
-
-
0028525572
-
Analysis of tyrosinase mutations associated with tyrosinase-related oculocutaneous albinism (OCA1)
-
Oetting WS, King RA. 1994. Analysis of tyrosinase mutations associated with tyrosinase-related oculocutaneous albinism (OCA1). Pigment Cell Res. 7:285-290.
-
(1994)
Pigment Cell Res
, vol.7
, pp. 285-290
-
-
Oetting, W.S.1
King, R.A.2
-
13
-
-
83255193089
-
TaqMan assays for genotyping 45 single nucleotide polymorphisms in the humpback whale nuclear genome
-
Polanowski A, Schmitt N, Double M, Jarman S. 2011. TaqMan assays for genotyping 45 single nucleotide polymorphisms in the humpback whale nuclear genome. Conserv Genet Resour. 3:645-649.
-
(2011)
Conserv Genet Resour
, vol.3
, pp. 645-649
-
-
Polanowski, A.1
Schmitt, N.2
Double, M.3
Jarman, S.4
-
14
-
-
25844488215
-
Tyrosinase and tyrosinase related protein I alleles specify domestic cat coat color phenotypes of the albino and brown loci
-
DOI 10.1093/jhered/esi066
-
Schmidt-Kûntzel A, Eizirik E, O'Brien SJ, Menotti-Raymon M. 2005. Tyrosinase and tyrosinase related protein 1 alleles specify domestic cat coat color phenotypes of the albino and brown loci. J Hered. 96:289-301. (Pubitemid 41399389)
-
(2005)
Journal of Heredity
, vol.96
, Issue.4
, pp. 289-301
-
-
Schmidt-Kuntzel, A.1
Eizirik, E.2
O'Brien, S.J.3
Menotti-Raymond, M.4
-
15
-
-
0347931983
-
A form of albinism in cattle is caused by a tyrosinase frameshift mutation
-
DOI 10.1007/s00335-002-2249-5
-
Schmutz SM, Berryere TG, Ciobanu DC, Mileham AJ, Schmidtz BH, Fredholm M. 2004. A form of albinism in cattle is caused by a tyrosinase frameshift mutation. Mamm Genome. 15:62-67. (Pubitemid 38096211)
-
(2004)
Mammalian Genome
, vol.15
, Issue.1
, pp. 62-67
-
-
Schmutz, S.M.1
Berryere, T.G.2
Ciobanu, D.C.3
Mileham, A.J.4
Schmidtz, B.H.5
Fredholm, M.6
-
16
-
-
0030749392
-
Mutational analysis of copper binding by human tyrosinase
-
Spritz RA, Ho L, Furumura M, Hearing VJ. 1997. Mutational analysis of copper binding by human tyrosinase. J Invest Dermatol. 109:207-212. (Pubitemid 27337337)
-
(1997)
Journal of Investigative Dermatology
, vol.109
, Issue.2
, pp. 207-212
-
-
Spritz, R.A.1
Ho, L.2
Furumura, M.3
Hearing Jr., V.J.4
-
17
-
-
0024433692
-
Human oculocutaneous albinism caused by single base insertion in the tyrosinase gene
-
Tomita Y, Takeda A, Okinaga S, Tagami H, Shibahara S. 1989. Human oculocutaneous albinism caused by a single base insertion in the tyrosinase gene. Biochem Biophys Res Commun. 164:990-996. (Pubitemid 19283942)
-
(1989)
Biochemical and Biophysical Research Communications
, vol.164
, Issue.3
, pp. 990-996
-
-
Tomita, Y.1
Takeda, A.2
Okinaga, S.3
Tagami, H.4
Shibahara, S.5
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