Tissue localization of the copper chaperone ATOX1 and its potential role in disease

Mammalian Genome

Volumn 13, Issue 10, 2002, Pages 563-568

  Moore, Steven D P ^a   Helmle, Karmon E ^a   Prat, Lisa M ^a   Cox, Diane W ^a  

^a UNIVERSITY OF ALBERTA   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CHAPERONE; COPPER; PROTEIN ATOX1; UNCLASSIFIED DRUG; ADENOSINE TRIPHOSPHATASE; ARABIDOPSIS PROTEIN; ATOX1 PROTEIN, HUMAN; ATOX1 PROTEIN, MOUSE; CARRIER PROTEIN; CATION TRANSPORT PROTEIN; CCH PROTEIN, ARABIDOPSIS; WILSON DISEASE PROTEIN;

ADULT; ANIMAL TISSUE; ARTICLE; CENTRAL VEIN; CLINICAL ARTICLE; COPPER METABOLISM; GENE MUTATION; GLOMERULUS; HENLE LOOP; HEPATIC VEIN; HOMEOSTASIS; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; JUXTAGLOMERULAR APPARATUS; KIDNEY; KIDNEY CORTEX; KIDNEY MEDULLA; LIVER; LIVER CELL; MENKES SYNDROME; MOUSE; NEPHRON; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; STORAGE DISEASE; WILSON DISEASE; ANIMAL; BAGG ALBINO MOUSE; GENETICS; IMMUNOLOGY; METABOLISM; MOUSE MUTANT; MUTATION; PATHOLOGY; TISSUE DISTRIBUTION;

ANIMALIA; GLOMERULUS;

ADENOSINE TRIPHOSPHATASES; ANIMALS; ARABIDOPSIS PROTEINS; CARRIER PROTEINS; CATION TRANSPORT PROTEINS; HUMANS; IMMUNOHISTOCHEMISTRY; KIDNEY; LIVER; MENKES KINKY HAIR SYNDROME; MICE; MICE, INBRED BALB C; MICE, MUTANT STRAINS; MOLECULAR CHAPERONES; MUTATION; TISSUE DISTRIBUTION;

EID: 0036800925     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00335-002-2172-9     Document Type: Article

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