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Neutral p H and copper ions promote eumelanogenesis after the dopachrome stage

https://doi.org/10.1111/pcmr.12137
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/9783527636150.ch6openalex-snapshot
Structure of Melanins
inferredcites →https://doi.org/10.1002/humu.20143openalex-snapshot
Single nucleotide polymorphisms in theMATP gene are associated with normal human pigmentation variation
inferredcites →https://doi.org/10.1002/j.1460-2075.1992.tb05082.xopenalex-snapshot
A second tyrosinase‐related protein, TRP‐2, is a melanogenic enzyme termed DOPAchrome tautomerase.
inferredcites →https://doi.org/10.1002/j.1460-2075.1992.tb05083.xopenalex-snapshot
A second tyrosinase‐related protein, TRP‐2, maps to and is mutated at the mouse slaty locus.
inferredcites →https://doi.org/10.1002/j.1460-2075.1994.tb06925.xopenalex-snapshot
Tyrosinase related protein 1 (TRP1) functions as a DHICA oxidase in melanin biosynthesis.
inferredcites →https://doi.org/10.1006/abio.1997.2079openalex-snapshot
Chemical Characterization of Eumelanins with Special Emphasis on 5,6-Dihydroxyindole-2-carboxylic Acid Content and Molecular Size
inferredcites →https://doi.org/10.1006/bbrc.2001.4315openalex-snapshot
Characterization of a Model Compound for the Lysine Tyrosylquinone Cofactor of Lysyl Oxidase
inferredcites →https://doi.org/10.1006/excr.2000.5092openalex-snapshot
Regulation of the Catalytic Activity of Preexisting Tyrosinase in Black and Caucasian Human Melanocyte Cell Cultures
inferredcites →https://doi.org/10.1006/excr.2001.5251openalex-snapshot
Melanosomal pH Controls Rate of Melanogenesis, Eumelanin/Phaeomelanin Ratio and Melanosome Maturation in Melanocytes and Melanoma Cells
inferredcites →https://doi.org/10.1016/0003-2697(88)90639-2openalex-snapshot
Preparation of eumelanin-related metabolites 5,6-dihydroxyindole, 5,6-dihydroxyindole-2-carboxylic acid, and their O-methyl derivatives
inferredcites →https://doi.org/10.1016/0006-291x(90)91011-gopenalex-snapshot
Dopachrome conversion factor functions as an isomerase
inferredcites →https://doi.org/10.1016/0304-4165(85)90048-0openalex-snapshot
A pulse radiolysis investigation of the oxidation of the melanin precursors 3,4-dihydroxyphenylalanine (dopa) and the cysteinyldopas
inferredcites →https://doi.org/10.1016/0304-4165(86)90146-7openalex-snapshot
Reexamination of the structure of eumelanin
inferredcites →https://doi.org/10.1016/0304-4165(87)90110-3openalex-snapshot
Effect of metal ions on the rearrangement of dopachrome
inferredcites →https://doi.org/10.1016/0304-4165(91)90003-yopenalex-snapshot
Comparative action of dopachrome tautomerase and metal ions on the rearrangement of dopachrome
inferredcites →https://doi.org/10.1016/j.ab.2012.12.005openalex-snapshot
High-performance liquid chromatography estimation of cross-linking of dihydroxyindole moiety in eumelanin
inferredcites →https://doi.org/10.1016/j.exer.2011.04.004openalex-snapshot
Chemical composition of melanosomes, lipofuscin and melanolipofuscin granules of human RPE tissues
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2007.11.021openalex-snapshot
TRP-2 specifically decreases WM35 cell sensitivity to oxidative stress
inferredcites →https://doi.org/10.1016/j.neuro.2009.07.006openalex-snapshot
Cytotoxicity of dopaminochrome in the mesencephalic cell line, MN9D, is dependent upon oxidative stress
inferredcites →https://doi.org/10.1016/j.yexcr.2004.04.033openalex-snapshot
The relationship between Na+/H+ exchanger expression and tyrosinase activity in human melanocytes
inferredcites →https://doi.org/10.1016/s0021-9258(17)32408-0openalex-snapshot
A new enzymatic function in the melanogenic pathway. The 5,6-dihydroxyindole-2-carboxylic acid oxidase activity of tyrosinase-related protein-1 (TRP1).
inferredcites →https://doi.org/10.1016/s0040-4020(01)87714-0openalex-snapshot
Sulphydryl compounds in melanogenesis
inferredcites →https://doi.org/10.1016/s0040-4020(02)00335-6openalex-snapshot
Atropoisomeric melanin intermediates by oxidation of the melanogenic precursor 5,6-dihydroxyindole-2-carboxylic acid under biomimetic conditions
inferredcites →https://doi.org/10.1038/nature07163openalex-snapshot
Cell-specific ATP7A transport sustains copper-dependent tyrosinase activity in melanosomes
inferredcites →https://doi.org/10.1038/nature09141openalex-snapshot
HIF-1 antagonizes p53-mediated apoptosis through a secreted neuronal tyrosinase
inferredcites →https://doi.org/10.1038/ng.160openalex-snapshot
Two newly identified genetic determinants of pigmentation in Europeans
inferredcites →https://doi.org/10.1038/ng1195-328openalex-snapshot
Variants of the melanocyte–stimulating hormone receptor gene are associated with red hair and fair skin in humans
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Determination of Melanin Synthetic Pathways
inferredcites →https://doi.org/10.1042/0264-6021:3540131openalex-snapshot
The 5,6-dihydroxyindole-2-carboxylic acid (DHICA) oxidase activity of human tyrosinase
inferredcites →https://doi.org/10.1074/jbc.m109.005819openalex-snapshot
αMSH and Cyclic AMP Elevating Agents Control Melanosome pH through a Protein Kinase A-independent Mechanism
inferredcites →https://doi.org/10.1093/hmg/9.19.2845openalex-snapshot
The Menkes copper transporter is required for the activation of tyrosinase
inferredcites →https://doi.org/10.1093/hmg/ddp003openalex-snapshot
Molecular genetics of human pigmentation diversity
inferredcites →https://doi.org/10.1093/molbev/msl203openalex-snapshot
Genetic Evidence for the Convergent Evolution of Light Skin in Europeans and East Asians
inferredcites →https://doi.org/10.1096/fj.11-201376openalex-snapshot
Cystinosin is a melanosomal protein that regulates melanin synthesis
inferredcites →https://doi.org/10.1111/1523-1747.ep12320792openalex-snapshot
Chemical Characterization of Hair Melanins in Various Coat-Color Mutants of Mice
inferredcites →https://doi.org/10.1111/j.1468-2494.2011.00691.xopenalex-snapshot
Age‐dependent changes in eumelanin composition in hairs of various ethnic origins
inferredcites →https://doi.org/10.1111/j.1468-3083.2011.04278.xopenalex-snapshot
Diversity of human hair pigmentation as studied by chemical analysis of eumelanin and pheomelanin
inferredcites →https://doi.org/10.1111/j.1556-4029.2009.01317.xopenalex-snapshot
Predicting Phenotype from Genotype: Normal Pigmentation*
inferredcites →https://doi.org/10.1111/j.1600-0749.2004.00170.xopenalex-snapshot
Absence of TRP‐2 in Melanogenic Melanocytes of Human Hair
inferredcites →https://doi.org/10.1111/j.1600-0749.2006.00327.xopenalex-snapshot
Dopaquinone redox exchange with dihydroxyindole and dihydroxyindole carboxylic acid
inferredcites →https://doi.org/10.1111/j.1751-1097.2005.tb01532.xopenalex-snapshot
Comparison of Structural and Chemical Properties of Black and Red Human Hair Melanosomes¶
inferredcites →https://doi.org/10.1111/j.1751-1097.2007.00238.xopenalex-snapshot
Chemistry of Mixed Melanogenesis—Pivotal Roles of Dopaquinone†
inferredcites →https://doi.org/10.1111/j.1751-1097.2010.00726.xopenalex-snapshot
Zinc‐induced Structural Effects Enhance Oxygen Consumption and Superoxide Generation in Synthetic Pheomelanins on UVA/Visible Light Irradiation†
inferredcites →https://doi.org/10.1111/j.1755-148x.2009.00580.xopenalex-snapshot
Chemical analysis of late stages of pheomelanogenesis: conversion of dihydrobenzothiazine to a benzothiazole structure
inferredcites →https://doi.org/10.1111/j.1755-148x.2009.00610.xopenalex-snapshot
Current challenges in understanding melanogenesis: bridging chemistry, biological control, morphology, and function
inferredcites →https://doi.org/10.1111/j.1755-148x.2010.00755.xopenalex-snapshot
Human hair melanins: what we have learned and have not learned from mouse coat color pigmentation
inferredcites →https://doi.org/10.1111/j.1755-148x.2011.00864.xopenalex-snapshot
Usefulness of alkaline hydrogen peroxide oxidation to analyze eumelanin and pheomelanin in various tissue samples: application to chemical analysis of human hair melanins
inferredcites →https://doi.org/10.1111/pcmr.12053openalex-snapshot
S lc45a2 and V ‐ ATP ase are regulators of melanosomal p H homeostasis in zebrafish, providing a mechanism for human pigment evolution and disease
inferredcites →https://doi.org/10.1111/pcmr.12121openalex-snapshot
Melanins and melanogenesis: methods, standards, protocols
inferredcites →https://doi.org/10.1126/science.1116238openalex-snapshot
SLC24A5, a Putative Cation Exchanger, Affects Pigmentation in Zebrafish and Humans
inferredcites →https://doi.org/10.1146/annurev.genet.37.110801.143233openalex-snapshot
Genetics of Hair and Skin Color
inferredcites →https://doi.org/10.1159/000247407openalex-snapshot
Menkes’ Disease: Report of a Case and Determination of Eumelanin and Pheomelanin in Hypopigmented Hair
inferredcites →https://doi.org/10.1562/2004-08-03-ra-259.1openalex-snapshot
Comparison of Structural and Chemical Properties of Black and Red Human Hair Melanosomes¶

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Melanins in Vertebrates
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Iron and copper ions accelerate and modify dopamine oxidation to eumelanin: implications for neuromelanin genesis
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Mechanism of dopachrome tautomerization into 5,6-dihydroxyindole-2-carboxylic acid catalyzed by Cu(II) based on quantum chemical calculations
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Characterization of a previously uncharacterized MelC2 tyrosinase from Streptomyces griseorubiginosus and development of a whole-cell catalytic system for DOPA-melanin production
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Identification of critical amino acid residues in the regulatory N-terminal domain of PMEL
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Pheomelanogenesis is promoted at a weakly acidic pH
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inferred← citeshttps://doi.org/10.7287/peerj.5215v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Ultrastructural alterations in the retinal pigment epithelium and photoreceptors of a Stargardt patient and three Stargardt mouse models: indication for the central role of RPE melanin in oxidative stress (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.5215v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Ultrastructural alterations in the retinal pigment epithelium and photoreceptors of a Stargardt patient and three Stargardt mouse models: indication for the central role of RPE melanin in oxidative stress (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.5215v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Ultrastructural alterations in the retinal pigment epithelium and photoreceptors of a Stargardt patient and three Stargardt mouse models: indication for the central role of RPE melanin in oxidative stress (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.5215v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Ultrastructural alterations in the retinal pigment epithelium and photoreceptors of a Stargardt patient and three Stargardt mouse models: indication for the central role of RPE melanin in oxidative stress (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.5215openalex-snapshot
Ultrastructural alterations in the retinal pigment epithelium and photoreceptors of a Stargardt patient and three Stargardt mouse models: indication for the central role of RPE melanin in oxidative stress
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