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PUBMED FOR HANDHELDS

Journal Abstract Search


280 related items for PubMed ID: 9367182

  • 1. Chemical characterization of pheomelanogenesis starting from dihydroxyphenylalanine or tyrosine and cysteine. Effects of tyrosinase and cysteine concentrations and reaction time.
    Ozeki H, Ito S, Wakamatsu K, Ishiguro I.
    Biochim Biophys Acta; 1997 Oct 20; 1336(3):539-48. PubMed ID: 9367182
    [Abstract] [Full Text] [Related]

  • 2. Pheomelanogenesis is promoted at a weakly acidic pH.
    Wakamatsu K, Nagao A, Watanabe M, Nakao K, Ito S.
    Pigment Cell Melanoma Res; 2017 May 20; 30(3):372-377. PubMed ID: 28271633
    [Abstract] [Full Text] [Related]

  • 3. Incorporation of sulfhydryl compounds into melanins in vitro.
    Ito S, Imai Y, Jimbow K, Fujita K.
    Biochim Biophys Acta; 1988 Jan 12; 964(1):1-7. PubMed ID: 3120789
    [Abstract] [Full Text] [Related]

  • 4. Optimization of conditions for preparing synthetic pheomelanin.
    Ito S.
    Pigment Cell Res; 1989 Jan 12; 2(1):53-6. PubMed ID: 2497445
    [Abstract] [Full Text] [Related]

  • 5. Co-regulation of melanin precursors and tyrosinase in human pigment cells: roles of cysteine and glutathione.
    Benathan M, Virador V, Furumura M, Kobayashi N, Panizzon RG, Hearing VJ.
    Cell Mol Biol (Noisy-le-grand); 1999 Nov 12; 45(7):981-90. PubMed ID: 10644002
    [Abstract] [Full Text] [Related]

  • 6. Mammalian tyrosinase catalyzes three reactions in the biosynthesis of melanin.
    Körner A, Pawelek J.
    Science; 1982 Sep 17; 217(4565):1163-5. PubMed ID: 6810464
    [Abstract] [Full Text] [Related]

  • 7. Chemical analysis of late stages of pheomelanogenesis: conversion of dihydrobenzothiazine to a benzothiazole structure.
    Wakamatsu K, Ohtara K, Ito S.
    Pigment Cell Melanoma Res; 2009 Aug 17; 22(4):474-86. PubMed ID: 19493317
    [Abstract] [Full Text] [Related]

  • 8. Chemical analysis of melanins and its application to the study of the regulation of melanogenesis.
    Ito S, Wakamatsu K, Ozeki H.
    Pigment Cell Res; 2000 Aug 17; 13 Suppl 8():103-9. PubMed ID: 11041366
    [Abstract] [Full Text] [Related]

  • 9. The role of sulfhydryl compounds in mammalian melanogenesis: the effect of cysteine and glutathione upon tyrosinase and the intermediates of the pathway.
    Jara JR, Aroca P, Solano F, Martinez JH, Lozano JA.
    Biochim Biophys Acta; 1988 Nov 17; 967(2):296-303. PubMed ID: 2903772
    [Abstract] [Full Text] [Related]

  • 10. Interaction of major coat color gene functions in mice as studied by chemical analysis of eumelanin and pheomelanin.
    Lamoreux ML, Wakamatsu K, Ito S.
    Pigment Cell Res; 2001 Feb 17; 14(1):23-31. PubMed ID: 11277491
    [Abstract] [Full Text] [Related]

  • 11. The effect of cysteine on oxidation of tyrosine, dopa, and cysteinyldopas.
    Agrup G, Hansson C, Rorsman H, Rosengren E.
    Arch Dermatol Res; 1982 Feb 17; 272(1-2):103-15. PubMed ID: 6819815
    [Abstract] [Full Text] [Related]

  • 12. Mammalian tyrosinase. A comparison of tyrosine hydroxylation and melanin formation.
    Hearing VJ, Ekel TM.
    Biochem J; 1976 Sep 01; 157(3):549-57. PubMed ID: 825109
    [Abstract] [Full Text] [Related]

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  • 14. Recent advances in the chemistry of melanogenesis in mammals.
    Prota G.
    J Invest Dermatol; 1980 Jul 01; 75(1):122-7. PubMed ID: 6771336
    [Abstract] [Full Text] [Related]

  • 15. From tyrosine to melanin: Signaling pathways and factors regulating melanogenesis.
    Rzepka Z, Buszman E, Beberok A, Wrześniok D.
    Postepy Hig Med Dosw (Online); 2016 Jun 30; 70(0):695-708. PubMed ID: 27356601
    [Abstract] [Full Text] [Related]

  • 16. Enhancement of pheomelanogenesis by L-dopa in the mouse melanocyte cell line, TM10, in vitro.
    Sato C, Ito S, Takeuchi T.
    J Cell Sci; 1987 May 30; 87 ( Pt 4)():507-12. PubMed ID: 2888776
    [Abstract] [Full Text] [Related]

  • 17. Chemistry of mixed melanogenesis--pivotal roles of dopaquinone.
    Ito S, Wakamatsu K.
    Photochem Photobiol; 2008 May 30; 84(3):582-92. PubMed ID: 18435614
    [Abstract] [Full Text] [Related]

  • 18. Protein-bound dopa and 5-S-cysteinyldopa in non-melanogenic tissues.
    Ito S, Jimbow K, Kato T, Kiyota M, Fujita K.
    Acta Derm Venereol; 1983 May 30; 63(6):463-7. PubMed ID: 6198833
    [Abstract] [Full Text] [Related]

  • 19. Ultraweak photon emission in model reactions of the in vitro formation of eumelanins and pheomelanins.
    Sławińska D, Sławiński J.
    Pigment Cell Res; 1987 May 30; 1(3):171-5. PubMed ID: 3149740
    [Abstract] [Full Text] [Related]

  • 20. High-performance liquid chromatography (HPLC) analysis of eu- and pheomelanin in melanogenesis control.
    Ito S.
    J Invest Dermatol; 1993 Feb 30; 100(2 Suppl):166S-171S. PubMed ID: 8433004
    [Abstract] [Full Text] [Related]


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