153 related articles for article (PubMed ID: 3134027)
1. Kinetic study of sinephrine oxidation by mushroom tyrosinase.
Garcia-Carmona F; Cabanes J; Garcia-Canovas F
Biochem Int; 1987 Jun; 14(6):1003-13. PubMed ID: 3134027
[TBL] [Abstract][Full Text] [Related]
2. Isoproterenol oxidation by tyrosinase: intermediates characterization and kinetic study.
Jiménez M; García-Cánovas F; García-Carmona F; Iborra JL; Lozano JA
Biochem Int; 1985 Jul; 11(1):51-9. PubMed ID: 2994673
[TBL] [Abstract][Full Text] [Related]
3. Pronounced formation of 5-OH-dopa at enzymatic oxidation of DOPA in the presence of ascorbic acid.
Hansson C; Rorsman H; Rosengren E
Acta Derm Venereol; 1981; 61(2):147-8. PubMed ID: 6165191
[TBL] [Abstract][Full Text] [Related]
4. The effect of polyamines on tyrosinase activity.
Galindo JD; Martinez JH; Lopez-Ballester JA; Peñafiel R; Solano F; Lozano JA
Biochem Int; 1987 Dec; 15(6):1151-8. PubMed ID: 3125836
[TBL] [Abstract][Full Text] [Related]
5. Mushroom tyrosinase has an ascorbate oxidase activity.
Ros JR; Rodríguez-López JN; Varón-Castellanos R; García-Canovas F
Biochem Mol Biol Int; 1995 Jun; 36(2):301-9. PubMed ID: 7663434
[TBL] [Abstract][Full Text] [Related]
6. Analysis and interpretation of the action mechanism of mushroom tyrosinase on monophenols and diphenols generating highly unstable o-quinones.
Fenoll LG; Rodríguez-López JN; García-Sevilla F; García-Ruiz PA; Varón R; García-Cánovas F; Tudela J
Biochim Biophys Acta; 2001 Jul; 1548(1):1-22. PubMed ID: 11451433
[TBL] [Abstract][Full Text] [Related]
7. Chemical modification of lysine residues in affinity purified mushroom tyrosinase.
Khan IA; Ali R
Indian J Biochem Biophys; 1987 Feb; 24(1):12-7. PubMed ID: 3114128
[No Abstract] [Full Text] [Related]
8. Kinetic study and intermediates identification of noradrenaline oxidation by tyrosinase.
Jimenez M; Garcia-Canovas F; Garcia-Carmona F; Lozano JA; Iborra JL
Biochem Pharmacol; 1984 Nov; 33(22):3689-97. PubMed ID: 6439211
[TBL] [Abstract][Full Text] [Related]
9. Chemical intermediates in dopamine oxidation by tyrosinase, and kinetic studies of the process.
Jimenez M; Garcia-Carmona F; Garcia-Canovas F; Iborra JL; Lozano JA; Martinez F
Arch Biochem Biophys; 1984 Dec; 235(2):438-48. PubMed ID: 6097187
[TBL] [Abstract][Full Text] [Related]
10. The influence of catechol structure on the suicide-inactivation of tyrosinase.
Ramsden CA; Stratford MR; Riley PA
Org Biomol Chem; 2009 Sep; 7(17):3388-90. PubMed ID: 19675891
[TBL] [Abstract][Full Text] [Related]
11. [Quantitative determination of phenoloxidase (EC 1.14.18.1). Absorption behavior of mushroom and potato tyrosinase].
Schmidt H
Dermatol Monatsschr; 1986; 172(5):276-81. PubMed ID: 3087800
[No Abstract] [Full Text] [Related]
12. Major primary cytotoxic product of 4-hydroxyanisole oxidation by mushroom tyrosinase is 4-methoxy ortho benzoquinone.
Naish S; Holden JL; Cooksey CJ; Riley PA
Pigment Cell Res; 1988; 1(6):382-5. PubMed ID: 3148922
[TBL] [Abstract][Full Text] [Related]
13. Ellagic acid: characterization as substrate of polyphenol oxidase.
Muñoz-Muñoz JL; Garcia-Molina F; Garcia-Molina M; Tudela J; García-Cánovas F; Rodriguez-Lopez JN
IUBMB Life; 2009 Feb; 61(2):171-7. PubMed ID: 18925653
[TBL] [Abstract][Full Text] [Related]
14. The adrenochrome pathway. A potential catabolic route for adrenaline metabolism in inflammatory disease.
Matthews SB; Hallett MB; Henderson AH; Campbell AK
Adv Myocardiol; 1985; 6():367-81. PubMed ID: 3992038
[TBL] [Abstract][Full Text] [Related]
15. Hydroxylation of 7-hydroxychlorpromazine by mushroom tyrosinase.
Grover TA; Piette LH; Manian AA
Adv Biochem Psychopharmacol; 1974; 9(0):561-9. PubMed ID: 4365285
[No Abstract] [Full Text] [Related]
16. pH-dependent interconvertible forms of mushroom tyrosinase with different kinetic properties.
Devi CC; Tripathi RK; Ramaiah A
Pigment Cell Res; 1989; 2(1):8-13. PubMed ID: 2497446
[TBL] [Abstract][Full Text] [Related]
17. Kinetic study of the transient phase of a chemical reaction system coupled to an enzymatically catalyzed step. Application to the oxidation of epinine by tyrosinase.
Escribano J; García M; García Cánovas F; García Carmona F; Varón R; Tudela J; Lozano JA
Biophys Chem; 1987 Jul; 27(1):15-25. PubMed ID: 3111559
[TBL] [Abstract][Full Text] [Related]
18. Model sclerotization studies. 4. Generation of N-acetylmethionyl catechol adducts during tyrosinase-catalyzed oxidation of catechols in the presence of N-acetylmethionine.
Sugumaran M; Nelson E
Arch Insect Biochem Physiol; 1998; 38(1):44-52. PubMed ID: 9589603
[TBL] [Abstract][Full Text] [Related]
19. Initial mushroom tyrosinase-catalysed oxidation product of 4-hydroxyanisole is 4-methoxy-ortho-benzoquinone.
Naish S; Cooksey CJ; Riley PA
Pigment Cell Res; 1988; 1(6):379-81. PubMed ID: 3148921
[TBL] [Abstract][Full Text] [Related]
20. The catalytic effect of tyrosinase upon oxidation of 2-hydroxyestradiol in presence of catechol.
Jacobsohn GM; Jacobsohn MK
Arch Biochem Biophys; 1984 Jul; 232(1):189-96. PubMed ID: 6430238
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]