The Menkes copper transporter is required for the activation of tyrosinase

Human Molecular Genetics

Volumn 9, Issue 19, 2000, Pages 2845-2851

  Petris, Michael J ^a,b   Strausak, Daniel ^a   Mercer, Julian F B ^a  

^a DEAKIN UNIVERSITY   (Australia)

^b UNIVERSITY OF MISSOURI   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; ADENOSINE TRIPHOSPHATE; ASPARTIC ACID; CARRIER PROTEIN; COPPER; CYTOCHROME C OXIDASE; DOPAMINE BETA MONOOXYGENASE; MELANIN; MONOPHENOL MONOOXYGENASE; PROTEIN LYSINE 6 OXIDASE; RECOMBINANT ENZYME;

ARTICLE; CELL MEMBRANE TRANSPORT; CELLULAR DISTRIBUTION; CHELATION; CONTROLLED STUDY; COPPER DEFICIENCY; COPPER METABOLISM; ENZYME ACTIVATION; ENZYME ACTIVITY; ENZYME LOCALIZATION; FIBROBLAST; GENE MUTATION; GENETIC RECOMBINATION; GOLGI COMPLEX; HUMAN; HUMAN CELL; HUMAN TISSUE; INTRACELLULAR TRANSPORT; MAMMAL CELL; MELANOGENESIS; MENKES SYNDROME; PATHOGENESIS; PIGMENTATION; PLASMID; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN PHOSPHORYLATION; TRANSPORT KINETICS; X CHROMOSOME LINKAGE;

MAMMALIA;

EID: 0034703872     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/9.19.2845     Document Type: Article

References (33)

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20. DNA enhances melanogenesis
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