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Journal Abstract Search

204 related items for PubMed ID: 3101741

  • 1. A kinetic study of the melanization pathway between L-tyrosine and dopachrome.
    Cabanes J, García-Cánovas F, Lozano JA, García-Carmona F.
    Biochim Biophys Acta; 1987 Feb 20; 923(2):187-95. PubMed ID: 3101741
    [Abstract] [Full Text] [Related]

  • 2. Analysis of a kinetic model for melanin biosynthesis pathway.
    Rodríguez-López JN, Tudela J, Varón R, García-Carmona F, García-Cánovas F.
    J Biol Chem; 1992 Feb 25; 267(6):3801-10. PubMed ID: 1740428
    [Abstract] [Full Text] [Related]

  • 3. Inhibitory effects of melanin monomers, dihydroxyindole-2-carboxylic acid (DHICA) and dihydroxyindole (DHI) on mammalian tyrosinase, with a special reference to the role of DHICA/DHI ratio in melanogenesis.
    Wilczek A, Mishima Y.
    Pigment Cell Res; 1995 Apr 25; 8(2):105-12. PubMed ID: 7659677
    [Abstract] [Full Text] [Related]

  • 4. Dopachrome conversion activity in Aedes aegypti: significance during melanotic encapsulation of parasites and cuticular tanning.
    Li J, Zhao X, Christensen BM.
    Insect Biochem Mol Biol; 1994 Dec 25; 24(10):1043-9. PubMed ID: 7703986
    [Abstract] [Full Text] [Related]

  • 5. The role of pH in the melanin biosynthesis pathway.
    Cánovas FG, García-Carmona F, Sánchez JV, Pastor JL, Teruel JA.
    J Biol Chem; 1982 Aug 10; 257(15):8738-44. PubMed ID: 6807981
    [Abstract] [Full Text] [Related]

  • 6. An electrometric method for the determination of tyrosinase activity.
    Solano-Muñoz F, Peñafiel R, Galindo JD.
    Biochem J; 1985 Aug 01; 229(3):573-8. PubMed ID: 2996485
    [Abstract] [Full Text] [Related]

  • 7. Dopachrome conversion: a possible control point in melanin biosynthesis.
    Körner AM, Pawelek J.
    J Invest Dermatol; 1980 Aug 01; 75(2):192-5. PubMed ID: 6774031
    [No Abstract] [Full Text] [Related]

  • 8. Dopachrome oxidoreductase: a new enzyme in the pigment pathway.
    Barber JI, Townsend D, Olds DP, King RA.
    J Invest Dermatol; 1984 Aug 01; 83(2):145-9. PubMed ID: 6432918
    [Abstract] [Full Text] [Related]

  • 9. Kinetic study on the effect of pH on the melanin biosynthesis pathway.
    Rodríguez-López JN, Tudela J, Varón R, García-Cánovas F.
    Biochim Biophys Acta; 1991 Feb 15; 1076(3):379-86. PubMed ID: 1900435
    [Abstract] [Full Text] [Related]

  • 10. Effect of L-ascorbic acid on the monophenolase activity of tyrosinase.
    Ros JR, Rodríguez-López JN, García-Cánovas F.
    Biochem J; 1993 Oct 01; 295 ( Pt 1)(Pt 1):309-12. PubMed ID: 8216233
    [Abstract] [Full Text] [Related]

  • 11. Mechanism of inhibition of melanogenesis by hydroquinone.
    Palumbo A, d'Ischia M, Misuraca G, Prota G.
    Biochim Biophys Acta; 1991 Jan 23; 1073(1):85-90. PubMed ID: 1899343
    [Abstract] [Full Text] [Related]

  • 12. Effect of ferrous ions on the monophenolase activity of tyrosinase.
    Ros JR, Rodríguez-López JN, García-Cánovas F.
    Biochim Biophys Acta; 1993 Jun 04; 1163(3):303-8. PubMed ID: 8507669
    [Abstract] [Full Text] [Related]

  • 13. Oxidation of tyrosine to dopachrome by peroxidase isolated from murine melanoma.
    Okun MR, Schley L, Ziegelstein R, Blair H.
    Physiol Chem Phys; 1982 Jun 04; 14(1):8-12. PubMed ID: 6294694
    [Abstract] [Full Text] [Related]

  • 14. Cooperation of dopachrome conversion factor with phenoloxidase in the eumelanin pathway in haemolymph of Locusta migratoria (Insecta).
    Cherqui A, Duvic B, Reibel C, Brehélin M.
    Insect Biochem Mol Biol; 1998 Nov 04; 28(11):839-48. PubMed ID: 9818385
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. Dopachrome conversion and dopa oxidase activities in recessive yellow mice. Catalytic activities of extracts from pheomelanic and eumelanic tissues.
    Lamoreux ML.
    J Hered; 1986 Sep 01; 77(5):337-40. PubMed ID: 3095419
    [Abstract] [Full Text] [Related]

  • 17. Singlet oxygen generation during the oxidation of L-tyrosine and L-dopa with mushroom tyrosinase.
    Miyaji A, Kohno M, Inoue Y, Baba T.
    Biochem Biophys Res Commun; 2016 Mar 18; 471(4):450-3. PubMed ID: 26898801
    [Abstract] [Full Text] [Related]

  • 18. Regulation of the final phase of mammalian melanogenesis. The role of dopachrome tautomerase and the ratio between 5,6-dihydroxyindole-2-carboxylic acid and 5,6-dihydroxyindole.
    Aroca P, Solano F, Salinas C, García-Borrón JC, Lozano JA.
    Eur J Biochem; 1992 Aug 15; 208(1):155-63. PubMed ID: 1511683
    [Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. Lag kinetics of tyrosinase: its physiological implications.
    Ramaiah A.
    Indian J Biochem Biophys; 1996 Oct 17; 33(5):349-56. PubMed ID: 9029814
    [Abstract] [Full Text] [Related]

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