A mutation in the ATP7B copper transporter causes reduced dopamine β-hydroxylase and norepinephrine in mouse adrenal

Neurochemical Research

Volumn 28, Issue 6, 2003, Pages 867-873

  Gerbasi, Vincent ^a   Lutsenko, Svetlana ^a   Lewis, Elaine J ^a  

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

ATP7B, copper; Dopamine hydroxylase; Norepinephrine; Wilson disease

Indexed keywords

ADRENALIN; CARRIER PROTEIN; CHROMOGRANIN A; DOPAMINE BETA MONOOXYGENASE; NORADRENALIN; UNCLASSIFIED DRUG; WILSON DISEASE PROTEIN;

ADRENAL GLAND; ANIMAL TISSUE; ARTICLE; CELL LEVEL; CHROMAFFIN CELL; CONTROLLED STUDY; ENZYME ACTIVE SITE; ENZYME METABOLISM; GENE EXPRESSION; GENE MUTATION; HOMEOSTASIS; MOUSE; NEUROENDOCRINOLOGY; NONHUMAN; PRIORITY JOURNAL; PROTEIN CONTENT; PROTEIN SYNTHESIS; SECRETORY VESICLE; WILSON DISEASE;

ADENOSINE TRIPHOSPHATASES; ADRENAL GLANDS; ANIMALS; BASE SEQUENCE; CATION TRANSPORT PROTEINS; DNA PRIMERS; DOPAMINE BETA-HYDROXYLASE; EPINEPHRINE; GENOTYPE; HEPATOLENTICULAR DEGENERATION; MICE; MICE, KNOCKOUT; NOREPINEPHRINE; REFERENCE VALUES; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION;

ANIMALIA;

EID: 0037409990     PISSN: 03643190     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1023219308890     Document Type: Article

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