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186 related items for PubMed ID: 32776353
1. 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; 68(4):823-831. PubMed ID: 32776353 [Abstract] [Full Text] [Related]
4. 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]
5. Effects of ultraviolet irradiation on melanogenesis from tyrosine, Dopa and dopamine: a matrix-assisted laser desorption/ionization mass spectrometric study. Bertazzo A, Favretto D, Costa CV, Allegri G, Traldi P. Rapid Commun Mass Spectrom; 2000 Sep 17; 14(19):1862-8. PubMed ID: 11006597 [Abstract] [Full Text] [Related]
6. 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 17; 8(2):105-12. PubMed ID: 7659677 [Abstract] [Full Text] [Related]
11. Modulating effects of a novel skin-lightening agent, alpha-lipoic acid derivative, on melanin production by the formation of DOPA conjugate products. Tsuji-Naito K, Hatani T, Okada T, Tehara T. Bioorg Med Chem; 2007 Mar 01; 15(5):1967-75. PubMed ID: 17218103 [Abstract] [Full Text] [Related]
12. 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]
16. 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]