[1]
Chen, S. R, Jiang, B, Zheng, J. X, Xu, G. Y, Li, J. Y, & Yang, N: Isolation and characterization of natural melanin derived from silky fowl (Gallus gallus domesticus Brisson). Food Chemistry, 111, 745−749. Chua, S. C, Tan, C. P, Mirhosseini, H, Lai, O. M, Long.
DOI: 10.1016/j.foodchem.2008.04.053
Google Scholar
[2]
Riley, P. A. (1997): Melanin. The International Journal of Biochemistry & Cell Biology, 29 (11), 1235−1239.
Google Scholar
[3]
Prota, G: Progress in the chemistry of melanins and related metabolites. Med. Res. Rev. 8: 525–556; (1988).
DOI: 10.1002/med.2610080405
Google Scholar
[4]
G. Prota: Melanins and Melagenesis, Academic, San Diego, (1992).
Google Scholar
[5]
Sarna, T: Properties and function of ocular melanin a photophysical view. J. Photochem. Photobiol. Biol. 12: 215–258; (1992).
Google Scholar
[6]
Wang, H. Pan, Y. Tang, X. & Huang, Z: Isolation and characterization of melanin from Osmanthus fragrans' seeds. LWT, 39, 496−502. (2006).
DOI: 10.1016/j.lwt.2005.04.001
Google Scholar
[7]
Wu, Y. Shan, L. Yang, S. & Ma, A: Identification and antioxidant activity of melanin isolated from Hypoxylon archeri, a companion fungus of Tremella fuciformis. Journal of Basic Microbiology, 48, 217−221. (2008).
DOI: 10.1002/jobm.200700366
Google Scholar
[8]
S.I. Kotob, S.L. Coon, E.J. Quintero, R.M. Weiner. Appl. Environ. Microbiol. 61 (1995) 1620.
Google Scholar
[9]
Crip pa R, Horak V, Prota G, Svoronos P, Wolfram L: Chemistry of melanins. In: Brossi A, ed. The Alkaloids. New York: Academic Press, Inc.; 1989. p.253–323.
DOI: 10.1016/s0099-9598(08)60085-1
Google Scholar
[10]
Waka matsu K, Fujikawa K, Zucca FA, Zecca L, Ito S: The structure of neuromelanin as studied by chemical degradative methods. J Neurochem 2003; 86: 1015–1023.
DOI: 10.1046/j.1471-4159.2003.01917.x
Google Scholar
[11]
Butler, M. J. and A. W. Day. 1998: Fungal melanins: a review. Can. J. Microbiol. 44: 1115–1136.
DOI: 10.1139/w98-119
Google Scholar
[12]
Bell, A. A., and M. H. Wheeler: Biosynthesis and functions of fungal melanins. Annu. Rev. Phytopathol. 24: 411–451. (1986).
DOI: 10.1146/annurev.py.24.090186.002211
Google Scholar
[13]
Polacheck, I., and K. J. Kwon-Chung: Melanogenesis in Cryptococcus neoformans. J. Gen. Microbiol. 134: 1037–1041. ( 1988).
DOI: 10.1099/00221287-134-4-1037
Google Scholar
[14]
Brumbaugh JA. Ultrastructural differences between forming eumelanin and pheomelanin as revealed by the pink-eye mutation in the fowl. Dev Bio 1968; 18: 375–390.
DOI: 10.1016/0012-1606(68)90047-x
Google Scholar
[15]
Sealy RC, Hyde JS, Felix CC, Menon IA, Prota G: Eumelanins and pheomelanins: Characterization by electron spin resonance spectroscopy. Science 1982; 217: 545–547.
DOI: 10.1126/science.6283638
Google Scholar
[16]
Ana M. Gómez-Marín , Carlos I. Sánchez: Thermal and mass spectroscopic characterization of a sulphur-containing bacterial melanin from Bacillus subtilis. Journal of Non-Crystalline Solids 356 (2010) 1576–1580.
DOI: 10.1016/j.jnoncrysol.2010.05.054
Google Scholar
[17]
U. Itoh: Enhancement of photoconductivity by detrapping in anth racene crystal. J. Phys. Soc. Jpn. 35 (1973) 515–517.
Google Scholar
[18]
S. Ito, K. Fujita: Microanalysis of eumelanin and pheomelanin in hair and melanomas by chemical degradation and liquid chromatography. Anal. Biochem. 144 (1985) 527–536.
DOI: 10.1016/0003-2697(85)90150-2
Google Scholar
[19]
M. Latocha, E. Chodurek, S. Kurkiewicz, L. Swiatkowska, T. Wilczok, J. Anal. Appl. Pyrol. 56 (2000) 89.
Google Scholar
[20]
N. Kollias, R.M. Sayre, L. Zeise, M.R. Chedekel. Photoprotection racene crystal. J. Phys. Soc. Jpn. 35 (1973) 515–517.
Google Scholar
[21]
Ito, S: Reexamination of the structure of eumelanin. Biochim. Biophys. Acta 883: 155–161; (1986).
Google Scholar
[22]
Manning, J. T., Bundred, P. E., & Henzi, P: Melanin and HIV in sub-Saharan Africa. Journal of Theoretical Biology, 223, 131−133. (2003).
DOI: 10.1016/s0022-5193(03)00070-5
Google Scholar
[23]
Sava, V. M., Yang, S. M., Hong, M. Y., Yang, P. C., & Huang, G. S: Isolation and characterization of melanic pigments derived from tea and tea polyphenols. Food Chemistry, 73, 117−184. (2001).
DOI: 10.1016/s0308-8146(00)00258-2
Google Scholar
[24]
Montefiori DC, Zhou J: Selection antiuinal activity of synthetic L-tyronsine and L-Dopa melanins against human immunodeficiency virus in vitro. Antiviral Res(1991), 1: 11~20.
DOI: 10.1016/0166-3542(91)90037-r
Google Scholar