Hitomi Tanaka
Sekimachi, 5113892, Japan
Last Updated: 09/26/2026
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Found 11 publications
Mechanistic Insights into Tyrosinase-Catalyzed Metabolism of Hydroquinone: Implications for the Etiology of Exogenous Ochronosis and Cytotoxicity to Melanocytes.
Journal: International journal of molecular sciences
Published: October 06, 2025
Exogenous ochronosis by hydroquinone is not caused by inhibition of homogentisate dioxygenase but potentially by tyrosinase-catalysed metabolism of hydroquinone.
Journal: The British journal of dermatology
Published: May 16, 2025
Pterostilbene, a Dimethyl Derivative of Resveratrol, Exerts Cytotoxic Effects on Melanin-Producing Cells through Metabolic Activation by Tyrosinase.
Journal: International journal of molecular sciences
Published: August 22, 2024
Corrigendum to "DOPA pheomelanin is increased in nigral neuromelanin of Parkinson's disease" [Prog. Neurobiol. 223 (2023) 102414].
Journal: Progress in neurobiology
Published: May 08, 2023
DOPA pheomelanin is increased in nigral neuromelanin of Parkinson's disease.
Journal: Progress in neurobiology
Published: May 20, 2022
Oxidative Transformations of 3,4-Dihydroxyphenylacetaldehyde Generate Potential Reactive Intermediates as Causative Agents for Its Neurotoxicity.
Journal: International journal of molecular sciences
Published: September 30, 2021
The Oxidation of Equol by Tyrosinase Produces a Unique Di-ortho-Quinone: Possible Implications for Melanocyte Toxicity.
Journal: International journal of molecular sciences
Published: July 22, 2021
The Oxidative Pathway to Dopamine-Protein Conjugates and Their Pro-Oxidant Activities: Implications for the Neurodegeneration of Parkinson's Disease.
Journal: International journal of molecular sciences
Published: April 16, 2019
The Pro-Oxidant Activity of Pheomelanin is Significantly Enhanced by UVA Irradiation: Benzothiazole Moieties Are More Reactive than Benzothiazine Moieties.
Journal: International journal of molecular sciences
Published: September 03, 2018
Reduction of the nitro group to amine by hydroiodic acid to synthesize o-aminophenol derivatives as putative degradative markers of neuromelanin.
Journal: Molecules (Basel, Switzerland)
Published: May 04, 2014
Showing 1-11 of 11
Last Updated: 09/26/2026