These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

159 related items for PubMed ID: 1740428

  • 1. 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]

  • 2. 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]

  • 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 20; 8(2):105-12. PubMed ID: 7659677
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Inhibitory effects of cupferron on the monophenolase and diphenolase activity of mushroom tyrosinase.
    Xie LP, Chen QX, Huang H, Liu XD, Chen HT, Zhang RQ.
    Int J Biochem Cell Biol; 2003 Dec 15; 35(12):1658-66. PubMed ID: 12962705
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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]

  • 8. 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]

  • 9. 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]

  • 10. 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]

  • 11. 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]

  • 12. 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 17; 77(5):337-40. PubMed ID: 3095419
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. 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]

  • 15. Study of tyrosine and dopa enantiomers as tyrosinase substrates initiating l- and d-melanogenesis pathways.
    Fernandez-Julia PJ, Tudela-Serrano J, Garcia-Molina F, Garcia-Canovas F, Garcia-Jimenez A, Munoz-Munoz JL.
    Biotechnol Appl Biochem; 2021 Aug 01; 68(4):823-831. PubMed ID: 32776353
    [Abstract] [Full Text] [Related]

  • 16. Opposite effects of peroxidase in the initial stages of tyrosinase-catalysed melanin biosynthesis.
    García-Molina F, Fenoll LG, Morote JC, García-Ruiz PA, Rodríguez-López JN, García-Cánovas F, Tudela J.
    Int J Biochem Cell Biol; 2005 Jun 01; 37(6):1179-96. PubMed ID: 15778083
    [Abstract] [Full Text] [Related]

  • 17. Melanin formation in the inner ear is catalyzed by a new tyrosine hydroxylase kinetically and structurally different from tyrosinase.
    Benedito E, Jiménez-Cervantes C, Pérez D, Cubillana JD, Solano F, Jiménez-Cervantes J, Meyer zum Gottesberge AM, Lozano JA, García-Borrón JC.
    Biochim Biophys Acta; 1997 Jul 19; 1336(1):59-72. PubMed ID: 9271251
    [Abstract] [Full Text] [Related]

  • 18. Dopachrome conversion: a possible control point in melanin biosynthesis.
    Körner AM, Pawelek J.
    J Invest Dermatol; 1980 Aug 19; 75(2):192-5. PubMed ID: 6774031
    [No Abstract] [Full Text] [Related]

  • 19. New tyrosinase inhibitory decapeptide: Molecular insights into the role of tyrosine residues.
    Ochiai A, Tanaka S, Imai Y, Yoshida H, Kanaoka T, Tanaka T, Taniguchi M.
    J Biosci Bioeng; 2016 Jun 19; 121(6):607-613. PubMed ID: 26589783
    [Abstract] [Full Text] [Related]

  • 20. Dopachrome oxidoreductase: a new enzyme in the pigment pathway.
    Barber JI, Townsend D, Olds DP, King RA.
    J Invest Dermatol; 1984 Aug 19; 83(2):145-9. PubMed ID: 6432918
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.