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Journal Abstract Search

183 related items for PubMed ID: 7886000

  • 1. Analysis of tyrosinase mutations associated with tyrosinase-related oculocutaneous albinism (OCA1).
    Oetting WS, King RA.
    Pigment Cell Res; 1994 Oct; 7(5):285-90. PubMed ID: 7886000
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  • 2. Mutations of the human tyrosinase gene associated with tyrosinase related oculocutaneous albinism (OCA1). Mutations in brief no. 204. Online.
    Oetting WS, Fryer JP, King RA.
    Hum Mutat; 1998 Oct; 12(6):433-4. PubMed ID: 10671066
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  • 3. Analysis of mutations in the copper B binding region associated with type I (tyrosinase-related) oculocutaneous albinism.
    Oetting WS, King RA.
    Pigment Cell Res; 1992 Nov; 5(5 Pt 2):274-8. PubMed ID: 1292009
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  • 4. Molecular analysis of type I-A (tyrosinase negative) oculocutaneous albinism.
    Oetting WS, King RA.
    Hum Genet; 1992 Nov; 90(3):258-62. PubMed ID: 1487241
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  • 11. Detection of 53 novel DNA variations within the tyrosinase gene and accumulation of mutations in 17 patients with albinism.
    Opitz S, Käsmann-Kellner B, Kaufmann M, Schwinger E, Zühlke C.
    Hum Mutat; 2004 Jun; 23(6):630-1. PubMed ID: 15146472
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  • 12. Molecular basis of oculocutaneous albinism type 1 in Lebanese patients.
    Zahed L, Zahreddine H, Noureddine B, Rebeiz N, Shakar N, Zalloua P, Haddad F.
    J Hum Genet; 2005 Jun; 50(6):317-319. PubMed ID: 15937636
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  • 13. Tyrosinase gene mutations in type I (tyrosinase-deficient) oculocutaneous albinism define two clusters of missense substitutions.
    Tripathi RK, Strunk KM, Giebel LB, Weleber RG, Spritz RA.
    Am J Med Genet; 1992 Jul 15; 43(5):865-71. PubMed ID: 1642278
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  • 14. Insertion/deletion mutations of type I oculocutaneous albinism in chinese patients from Taiwan.
    Tsai CH, Tsai FJ, Wu JY, Lin SP, Chang JG, Yang CF, Lee CC.
    Hum Mutat; 1999 Dec 15; 14(6):542. PubMed ID: 10571953
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  • 15. Mutational analysis of copper binding by human tyrosinase.
    Spritz RA, Ho L, Furumura M, Hearing VJ.
    J Invest Dermatol; 1997 Aug 15; 109(2):207-12. PubMed ID: 9242509
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  • 16. Cloning and sequence analysis of the tyrosinase gene from a patient with tyrosinase-positive oculocutaneous albinism.
    Matsunaga J, Takeda A, Tomita Y, Hara M, Shibahara S, Tagami H.
    J Dermatol Sci; 1992 May 15; 3(3):181-5. PubMed ID: 1498098
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  • 17. 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. PubMed ID: 9163730
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  • 18. Computational analysis of histidine mutations on the structural stability of human tyrosinases leading to albinism insurgence.
    Hassan M, Abbas Q, Raza H, Moustafa AA, Seo SY.
    Mol Biosyst; 2017 Jul 25; 13(8):1534-1544. PubMed ID: 28640309
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