Developmental expression of the mouse mottled and toxic milk genes suggests distinct functions for the Menkes and Wilson disease copper transporters

Human Molecular Genetics

Volumn 6, Issue 7, 1997, Pages 1043-1049

  Kuo, Yien Ming ^a   Gitschier, Jane ^a   Packman, Seymour ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COPPER; METALLOPROTEIN;

ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRONCHUS; CENTRAL NERVOUS SYSTEM; CHOROID PLEXUS; CONTROLLED STUDY; COPPER METABOLISM; DEVELOPMENTAL GENETICS; DISORDERS OF METAL METABOLISM; EMBRYO; EMBRYO DEVELOPMENT; GENE MUTATION; HEART; IN SITU HYBRIDIZATION; INTESTINE; LIVER; LUNG; MENKES SYNDROME; MILK; MOUSE; NASOPHARYNX; NONHUMAN; PRIORITY JOURNAL; RESPIRATORY EPITHELIUM; RNA HYBRIDIZATION; THYMUS; TOXICITY; TRACHEA; WILSON DISEASE;

ADENOSINE TRIPHOSPHATASES; ANIMALS; CARRIER PROTEINS; CATION TRANSPORT PROTEINS; COPPER; EMBRYO; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HEPATOLENTICULAR DEGENERATION; HOMEOSTASIS; HUMANS; IN SITU HYBRIDIZATION; MENKES KINKY HAIR SYNDROME; MICE; RECOMBINANT FUSION PROTEINS; TISSUE DISTRIBUTION;

ANIMALIA; BRONCHUS;

EID: 0030751819     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/6.7.1043     Document Type: Article

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