Ctr1 drives intestinal copper absorption and is essential for growth, iron metabolism, and neonatal cardiac function

Cell Metabolism

Volumn 4, Issue 3, 2006, Pages 235-244

  Nose, Yasuhiro ^a   Kim, Byung Eun ^a   Thiele, Dennis J ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

HUMDISEASE

Indexed keywords

COPPER; COPPER SULFATE; FREE RADICAL; IRON; MEMBRANE PROTEIN; PROTEIN CTR1; UNCLASSIFIED DRUG;

ANGIOGENESIS; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BINDING AFFINITY; CELL SPECIFICITY; CONTROLLED STUDY; COPPER DEFICIENCY; COPPER METABOLISM; DETOXIFICATION; ENERGY RESOURCE; FEMALE; GROWTH DISORDER; HEART FUNCTION; HEART HYPERTROPHY; INTESTINE ABSORPTION; INTESTINE EPITHELIUM CELL; IRON METABOLISM; IRON OVERLOAD; KNOCKOUT MOUSE; MALE; MEMBRANE TRANSPORT; MOUSE; NONHUMAN; PRIORITY JOURNAL;

ANIMALS; ANIMALS, NEWBORN; CARDIOMEGALY; CATION TRANSPORT PROTEINS; CELL MEMBRANE; COPPER; DISEASE MODELS, ANIMAL; DWARFISM; HEART DEFECTS, CONGENITAL; INTESTINAL ABSORPTION; INTESTINAL MUCOSA; INTESTINES; IRON; MALABSORPTION SYNDROMES; MEMBRANE TRANSPORT PROTEINS; MICE; MICE, KNOCKOUT;

MAMMALIA;

EID: 33747849534     PISSN: 15504131     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cmet.2006.08.009     Document Type: Article

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