2001
DOI: 10.1006/abio.2000.4976
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Relationship of Melanin Degradation Products to Actual Melanin Content: Application to Human Hair

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Cited by 84 publications
(68 citation statements)
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“…In the presence of cysteine or glutathione, dopaquinone is converted to cysteinyl DOPA or glutathione DOPA. Subsequently, pheomelanin, a yellowred pigment, is formed (Raper, 1928;Kobayashi et al, 1995;Borges et al, 2001), presented in simplified form in Fig. 2.…”
Section: Melanin Formation and Distribution In The Skinmentioning
confidence: 97%
“…In the presence of cysteine or glutathione, dopaquinone is converted to cysteinyl DOPA or glutathione DOPA. Subsequently, pheomelanin, a yellowred pigment, is formed (Raper, 1928;Kobayashi et al, 1995;Borges et al, 2001), presented in simplified form in Fig. 2.…”
Section: Melanin Formation and Distribution In The Skinmentioning
confidence: 97%
“…[30] Generalizing, dark hairs have more melanin and more photosensitive amino acids than light hairs. Melanin can attribute photoprotection to hair protein, but only in the cortex.…”
Section: Photolightening Of Hair Melaninmentioning
confidence: 99%
“…According to Borges et al [27], black hair contains more or less 99% eumelanin and 1% pheomelanin, darkbrown and blond hairs 95% and 5%, and red hair 67% and 33%. These authors quantified the amounts of eumelanin and pheomelanin of 44 volunteers with different hair types.…”
Section: Susceptibility Of the Different Hair Types To Photodegradationmentioning
confidence: 99%