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174 related items for PubMed ID: 25736709

  • 1. A nonsense nucleotide substitution in the oculocutaneous albinism II gene underlies the original pink-eyed dilution allele (Oca2(p)) in mice.
    Shoji H, Kiniwa Y, Okuyama R, Yang M, Higuchi K, Mori M.
    Exp Anim; 2015; 64(2):171-9. PubMed ID: 25736709
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  • 2. Identification of P gene mutations in individuals with oculocutaneous albinism in sub-Saharan Africa.
    Kerr R, Stevens G, Manga P, Salm S, John P, Haw T, Ramsay M.
    Hum Mutat; 2000; 15(2):166-72. PubMed ID: 10649493
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  • 3. l-tyrosine induces melanocyte differentiation in novel pink-eyed dilution castaneus mouse mutant showing age-related pigmentation.
    Hirobe T, Ishikawa A.
    J Dermatol Sci; 2015 Dec; 80(3):203-11. PubMed ID: 26475433
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  • 6. Development of a novel pink-eyed dilution mouse model showing progressive darkening of the eyes and coat hair with aging.
    Ishikawa A, Sugiyama M, Hondo E, Kinoshita K, Yamagishi Y.
    Exp Anim; 2015 Dec; 64(2):207-20. PubMed ID: 25739360
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  • 9. The mouse p (pink-eyed dilution) and human P genes, oculocutaneous albinism type 2 (OCA2), and melanosomal pH.
    Brilliant MH.
    Pigment Cell Res; 2001 Apr; 14(2):86-93. PubMed ID: 11310796
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  • 10. Complementation of hypopigmentation in p-mutant (pink-eyed dilution) mouse melanocytes by normal human P cDNA, and defective complementation by OCA2 mutant sequences.
    Sviderskaya EV, Bennett DC, Ho L, Bailin T, Lee ST, Spritz RA.
    J Invest Dermatol; 1997 Jan; 108(1):30-4. PubMed ID: 8980282
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  • 12. The mouse pink-eyed dilution gene: association with hypopigmentation in Prader-Willi and Angelman syndromes and with human OCA2.
    Brilliant MH, King R, Francke U, Schuffenhauer S, Meitinger T, Gardner JM, Durham-Pierre D, Nakatsu Y.
    Pigment Cell Res; 1994 Dec; 7(6):398-402. PubMed ID: 7761348
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  • 15. Inheritance of a novel mutated allele of the OCA2 gene associated with high incidence of oculocutaneous albinism in a Polynesian community.
    Johanson HC, Chen W, Wicking C, Sturm RA.
    J Hum Genet; 2010 Feb; 55(2):103-11. PubMed ID: 20019752
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  • 17. In Southern Africa, brown oculocutaneous albinism (BOCA) maps to the OCA2 locus on chromosome 15q: P-gene mutations identified.
    Manga P, Kromberg J, Turner A, Jenkins T, Ramsay M.
    Am J Hum Genet; 2001 Mar; 68(3):782-7. PubMed ID: 11179026
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  • 18. Organization and sequence of the human P gene and identification of a new family of transport proteins.
    Lee ST, Nicholls RD, Jong MT, Fukai K, Spritz RA.
    Genomics; 1995 Mar 20; 26(2):354-63. PubMed ID: 7601462
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