Copper accumulation and compartmentalization in mouse fibroblast lacking metallothionein and copper chaperone, Atox1

Toxicology and Applied Pharmacology

Volumn 237, Issue 2, 2009, Pages 205-213

  Miyayama, Takamitsu ^a,b   Suzuki, Kazuo T ^a   Ogra, Yasumitsu ^a,b  

^a CHIBA UNIVERSITY   (Japan)

^b SHOWA PHARMACEUTICAL UNIVERSITY   (Japan)

Author keywords

Atox1; Copper; CS1; Ctr1; Metallothionein

Indexed keywords

ATOX1 PROTEIN; CCS PROTEIN; CHAPERONE; COPPER; COPPER EXPORTING ADENOSINE TRIPHOSPHATASE; CTR1 PROTEIN; FLUORESCENT DYE; METALLOTHIONEIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; BIOACCUMULATION; CELL COMPARTMENTALIZATION; CELL LEVEL; CELLULAR DISTRIBUTION; CONTROLLED STUDY; COPPER DEFICIENCY; CYTOPLASM VESICLE; DETOXIFICATION; ENZYME ACTIVE SITE; FIBROBLAST; HOMEOSTASIS; IMAGING SYSTEM; KNOCKOUT GENE; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; OXIDATION REDUCTION REACTION; PROTEIN FUNCTION; REGULATORY MECHANISM; TECHNIQUE;

ANIMALS; CATION TRANSPORT PROTEINS; CELL LINE; COPPER; FIBROBLASTS; GENE EXPRESSION REGULATION; GENE SILENCING; METALLOTHIONEIN; MICE; MICE, KNOCKOUT; MOLECULAR CHAPERONES; RNA, SMALL INTERFERING;

MAMMALIA;

EID: 67349118440     PISSN: 0041008X     EISSN: 10960333     Source Type: Journal    
DOI: 10.1016/j.taap.2009.03.024     Document Type: Article

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