152 related articles for article (PubMed ID: 1946209)
1. After dopachrome?
Pawelek JM
Pigment Cell Res; 1991 Mar; 4(2):53-62. PubMed ID: 1946209
[TBL] [Abstract][Full Text] [Related]
2. 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; 8(2):105-12. PubMed ID: 7659677
[TBL] [Abstract][Full Text] [Related]
3. Synthesis and characterization of melanins from dihydroxyindole-2-carboxylic acid and dihydroxyindole.
Orlow SJ; Osber MP; Pawelek JM
Pigment Cell Res; 1992 Sep; 5(3):113-21. PubMed ID: 1409448
[TBL] [Abstract][Full Text] [Related]
4. 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; 208(1):155-63. PubMed ID: 1511683
[TBL] [Abstract][Full Text] [Related]
5. Function of dopachrome oxidoreductase and metal ions in dopachrome conversion in the eumelanin pathway.
Leonard LJ; Townsend D; King RA
Biochemistry; 1988 Aug; 27(16):6156-9. PubMed ID: 3142518
[TBL] [Abstract][Full Text] [Related]
6. Dopachrome oxidoreductase: a new enzyme in the pigment pathway.
Barber JI; Townsend D; Olds DP; King RA
J Invest Dermatol; 1984 Aug; 83(2):145-9. PubMed ID: 6432918
[TBL] [Abstract][Full Text] [Related]
7. Effect of pH on elementary steps of dopachrome conversion from first-principles calculation.
Kishida R; Ushijima Y; Saputro AG; Kasai H
Pigment Cell Melanoma Res; 2014 Sep; 27(5):734-43. PubMed ID: 24807014
[TBL] [Abstract][Full Text] [Related]
8. Dopachrome tautomerase decreases the binding of indolic melanogenesis intermediates to proteins.
Salinas C; García-Borrón JC; Solano F; Lozano JA
Biochim Biophys Acta; 1994 Jan; 1204(1):53-60. PubMed ID: 8305475
[TBL] [Abstract][Full Text] [Related]
9. Neutral pH and copper ions promote eumelanogenesis after the dopachrome stage.
Ito S; Suzuki N; Takebayashi S; Commo S; Wakamatsu K
Pigment Cell Melanoma Res; 2013 Nov; 26(6):817-25. PubMed ID: 23844795
[TBL] [Abstract][Full Text] [Related]
10. 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; 70(0):695-708. PubMed ID: 27356601
[TBL] [Abstract][Full Text] [Related]
11. Isolation of a new tautomerase monitored by the conversion of D-dopachrome to 5,6-dihydroxyindole.
Odh G; Hindemith A; Rosengren AM; Rosengren E; Rorsman H
Biochem Biophys Res Commun; 1993 Dec; 197(2):619-24. PubMed ID: 8267597
[TBL] [Abstract][Full Text] [Related]
12. Quinone methide as a new intermediate in eumelanin biosynthesis.
Sugumaran M; Semensi V
J Biol Chem; 1991 Apr; 266(10):6073-8. PubMed ID: 2007565
[TBL] [Abstract][Full Text] [Related]
13. Mechanism of dopachrome tautomerization into 5,6-dihydroxyindole-2-carboxylic acid catalyzed by Cu(II) based on quantum chemical calculations.
Kishida R; Saputro AG; Kasai H
Biochim Biophys Acta; 2015 Feb; 1850(2):281-6. PubMed ID: 25450182
[TBL] [Abstract][Full Text] [Related]
14. DHICA oxidase activity of TRP1 and interactions with other melanogenic enzymes.
Kobayashi T; Urabe K; Winder A; Tsukamoto K; Brewington T; Imokawa G; Potterf B; Hearing VJ
Pigment Cell Res; 1994 Aug; 7(4):227-34. PubMed ID: 7855068
[TBL] [Abstract][Full Text] [Related]
15. Dopachrome conversion factor functions as an isomerase.
Pawelek JM
Biochem Biophys Res Commun; 1990 Feb; 166(3):1328-33. PubMed ID: 2106316
[TBL] [Abstract][Full Text] [Related]
16. Effect of aluminum (III) on the conversion of dopachrome in the melanin synthesis pathway.
Di J; Bi S
Spectrochim Acta A Mol Biomol Spectrosc; 2003 Jun; 59(8):1689-96. PubMed ID: 12736054
[TBL] [Abstract][Full Text] [Related]
17. Regulatory factors for polymerization of melanin monomers within coated vesicles and premelanosomes in melanoma cells.
Wilczek A; Mishima Y
Melanoma Res; 1993 Aug; 3(4):255-62. PubMed ID: 8219758
[TBL] [Abstract][Full Text] [Related]
18. Synthesis in vitro of 5,6-dihydroxyindole-2-carboxylic acid by dopachrome conversion factor from Cloudman S91 melanoma cells.
Korner AM; Gettins P
J Invest Dermatol; 1985 Sep; 85(3):229-31. PubMed ID: 4031539
[TBL] [Abstract][Full Text] [Related]
19. Regulation of DHICA-mediated antioxidation by dopachrome tautomerase: implication for skin photoprotection against UVA radiation.
Jiang S; Liu XM; Dai X; Zhou Q; Lei TC; Beermann F; Wakamatsu K; Xu SZ
Free Radic Biol Med; 2010 May; 48(9):1144-51. PubMed ID: 20123016
[TBL] [Abstract][Full Text] [Related]
20. 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; 257(15):8738-44. PubMed ID: 6807981
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
