Intracellular localization and loss of copper responsiveness of Mnk, the murine homologue of the Menkes protein, in cells from blotchy (Mo(blo)) and brindled (Mo(br) mouse mutants

Human Molecular Genetics

Volumn 8, Issue 6, 1999, Pages 1069-1075

  La Fontaine, Sharon ^a,d   Firth, Stephen D ^a,d   Lockhart, Paul J ^a   Brooks, Hilary ^b   Camakaris, James ^b   Mercer, Julian F B ^a,c,d  

^a ROYAL CHILDREN'S HOSPITAL   (Australia)

^b UNIVERSITY OF MELBOURNE   (Australia)

^c DEAKIN UNIVERSITY   (Australia)

^d Ctr for Cell and Molecular Biology   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; COPPER;

ANIMAL CELL; ANIMAL MODEL; ARTICLE; CELL CULTURE; COPPER DEFICIENCY; GENE MUTATION; MENKES SYNDROME; MOUSE; NONHUMAN; OCCIPITAL LOBE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN LOCALIZATION; SEQUENCE HOMOLOGY; X CHROMOSOME LINKAGE;

ADENOSINE TRIPHOSPHATASES; AMINO ACID SEQUENCE; ANIMALS; CARRIER PROTEINS; CATION TRANSPORT PROTEINS; CELL LINE; CHO CELLS; COPPER; CRICETINAE; DNA, COMPLEMENTARY; FIBROBLASTS; FLUORESCENT ANTIBODY TECHNIQUE, INDIRECT; HUMANS; MENKES KINKY HAIR SYNDROME; MICE; MICE, MUTANT STRAINS; MUTATION; RECOMBINANT FUSION PROTEINS;

ANIMALIA; MURINAE;

EID: 0033046222     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/8.6.1069     Document Type: Article

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